RU2016129536A - Препараты на основе терпенов и каннабиноидов - Google Patents
Препараты на основе терпенов и каннабиноидов Download PDFInfo
- Publication number
- RU2016129536A RU2016129536A RU2016129536A RU2016129536A RU2016129536A RU 2016129536 A RU2016129536 A RU 2016129536A RU 2016129536 A RU2016129536 A RU 2016129536A RU 2016129536 A RU2016129536 A RU 2016129536A RU 2016129536 A RU2016129536 A RU 2016129536A
- Authority
- RU
- Russia
- Prior art keywords
- terpene
- pinene
- group
- myrcene
- terpenes
- Prior art date
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- 235000007586 terpenes Nutrition 0.000 title claims 48
- 229930003827 cannabinoid Natural products 0.000 title claims 13
- 239000003557 cannabinoid Substances 0.000 title claims 13
- 238000002360 preparation method Methods 0.000 title claims 4
- 150000003505 terpenes Chemical class 0.000 claims 44
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 claims 26
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 claims 19
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims 14
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 claims 13
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 claims 12
- 229940079593 drug Drugs 0.000 claims 11
- 239000003814 drug Substances 0.000 claims 11
- FAMPSKZZVDUYOS-UHFFFAOYSA-N 2,6,6,9-tetramethylcycloundeca-1,4,8-triene Chemical compound CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 claims 10
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 claims 10
- -1 cannadibiol Chemical compound 0.000 claims 10
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims 10
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 claims 10
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 claims 8
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 claims 8
- RGZSQWQPBWRIAQ-CABCVRRESA-N (-)-alpha-Bisabolol Chemical compound CC(C)=CCC[C@](C)(O)[C@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-CABCVRRESA-N 0.000 claims 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 8
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 claims 8
- RGZSQWQPBWRIAQ-LSDHHAIUSA-N alpha-Bisabolol Natural products CC(C)=CCC[C@@](C)(O)[C@@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-LSDHHAIUSA-N 0.000 claims 8
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 claims 8
- 229930006722 beta-pinene Natural products 0.000 claims 8
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 claims 8
- 239000001500 (2R)-6-methyl-2-[(1R)-4-methyl-1-cyclohex-3-enyl]hept-5-en-2-ol Substances 0.000 claims 7
- 235000001510 limonene Nutrition 0.000 claims 7
- 229940087305 limonene Drugs 0.000 claims 7
- 239000000725 suspension Substances 0.000 claims 7
- 229940065144 cannabinoids Drugs 0.000 claims 6
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 claims 5
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 claims 5
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 claims 5
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 claims 5
- PSVBPLKYDMHILE-UHFFFAOYSA-N alpha-humulene Natural products CC1=C/CC(C)(C)C=CCC=CCC1 PSVBPLKYDMHILE-UHFFFAOYSA-N 0.000 claims 5
- 229940088601 alpha-terpineol Drugs 0.000 claims 5
- 229930007744 linalool Natural products 0.000 claims 5
- 239000002502 liposome Substances 0.000 claims 5
- YCBKSSAWEUDACY-IAGOWNOFSA-N 11-hydroxy-Delta(9)-tetrahydrocannabinol Chemical compound C1=C(CO)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 YCBKSSAWEUDACY-IAGOWNOFSA-N 0.000 claims 4
- CYQFCXCEBYINGO-UHFFFAOYSA-N THC Natural products C1=C(C)CCC2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3C21 CYQFCXCEBYINGO-UHFFFAOYSA-N 0.000 claims 4
- CYQFCXCEBYINGO-IAGOWNOFSA-N delta1-THC Chemical compound C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 CYQFCXCEBYINGO-IAGOWNOFSA-N 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- ZTGXAWYVTLUPDT-UHFFFAOYSA-N cannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1C1C(C(C)=C)CC=C(C)C1 ZTGXAWYVTLUPDT-UHFFFAOYSA-N 0.000 claims 3
- 150000007823 ocimene derivatives Chemical class 0.000 claims 3
- 239000000243 solution Substances 0.000 claims 3
- XJPBRODHZKDRCB-UHFFFAOYSA-N trans-alpha-ocimene Natural products CC(=C)CCC=C(C)C=C XJPBRODHZKDRCB-UHFFFAOYSA-N 0.000 claims 3
- BQOFWKZOCNGFEC-DTWKUNHWSA-N (-)-Delta(3)-carene Chemical compound C1C(C)=CC[C@@H]2C(C)(C)[C@H]12 BQOFWKZOCNGFEC-DTWKUNHWSA-N 0.000 claims 2
- AOYYFUGUUIRBML-IAGOWNOFSA-N (6ar,10ar)-6,6-dimethyl-9-methylidene-3-pentyl-7,8,10,10a-tetrahydro-6ah-benzo[c]chromen-1-ol Chemical compound C1C(=C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 AOYYFUGUUIRBML-IAGOWNOFSA-N 0.000 claims 2
- YCBKSSAWEUDACY-UHFFFAOYSA-N 7-Hydroxy-Delta1-THC Natural products C1=C(CO)CCC2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3C21 YCBKSSAWEUDACY-UHFFFAOYSA-N 0.000 claims 2
- VBGLYOIFKLUMQG-UHFFFAOYSA-N Cannabinol Chemical compound C1=C(C)C=C2C3=C(O)C=C(CCCCC)C=C3OC(C)(C)C2=C1 VBGLYOIFKLUMQG-UHFFFAOYSA-N 0.000 claims 2
- XXGMIHXASFDFSM-UHFFFAOYSA-N Delta9-tetrahydrocannabinol Natural products CCCCCc1cc2OC(C)(C)C3CCC(=CC3c2c(O)c1O)C XXGMIHXASFDFSM-UHFFFAOYSA-N 0.000 claims 2
- CYQFCXCEBYINGO-DLBZAZTESA-N Dronabinol Natural products C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@H]21 CYQFCXCEBYINGO-DLBZAZTESA-N 0.000 claims 2
- 229960003453 cannabinol Drugs 0.000 claims 2
- HCAWPGARWVBULJ-IAGOWNOFSA-N delta8-THC Chemical compound C1C(C)=CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 HCAWPGARWVBULJ-IAGOWNOFSA-N 0.000 claims 2
- 229960004242 dronabinol Drugs 0.000 claims 2
- 229950005812 levonantradol Drugs 0.000 claims 2
- FFVXQGMUHIJQAO-BFKQJKLPSA-N levonantradol Chemical compound C([C@@H](C)OC=1C=C(OC(C)=O)C=2[C@@H]3C[C@H](O)CC[C@H]3[C@H](C)NC=2C=1)CCC1=CC=CC=C1 FFVXQGMUHIJQAO-BFKQJKLPSA-N 0.000 claims 2
- GECBBEABIDMGGL-RTBURBONSA-N nabilone Chemical compound C1C(=O)CC[C@H]2C(C)(C)OC3=CC(C(C)(C)CCCCCC)=CC(O)=C3[C@@H]21 GECBBEABIDMGGL-RTBURBONSA-N 0.000 claims 2
- 229960002967 nabilone Drugs 0.000 claims 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 2
- WTVHAMTYZJGJLJ-UHFFFAOYSA-N (+)-(4S,8R)-8-epi-beta-bisabolol Natural products CC(C)=CCCC(C)C1(O)CCC(C)=CC1 WTVHAMTYZJGJLJ-UHFFFAOYSA-N 0.000 claims 1
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 claims 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims 1
- 229920002261 Corn starch Polymers 0.000 claims 1
- 108010010803 Gelatin Proteins 0.000 claims 1
- 229920002907 Guar gum Polymers 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- QHMBSVQNZZTUGM-UHFFFAOYSA-N Trans-Cannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1C1C(C(C)=C)CCC(C)=C1 QHMBSVQNZZTUGM-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 229940072056 alginate Drugs 0.000 claims 1
- 235000010443 alginic acid Nutrition 0.000 claims 1
- 229920000615 alginic acid Polymers 0.000 claims 1
- 125000003447 alpha-pinene group Chemical group 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 229940036350 bisabolol Drugs 0.000 claims 1
- HHGZABIIYIWLGA-UHFFFAOYSA-N bisabolol Natural products CC1CCC(C(C)(O)CCC=C(C)C)CC1 HHGZABIIYIWLGA-UHFFFAOYSA-N 0.000 claims 1
- QHMBSVQNZZTUGM-ZWKOTPCHSA-N cannabidiol Chemical compound OC1=CC(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)=C)CCC(C)=C1 QHMBSVQNZZTUGM-ZWKOTPCHSA-N 0.000 claims 1
- 229950011318 cannabidiol Drugs 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 235000010980 cellulose Nutrition 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 239000008120 corn starch Substances 0.000 claims 1
- PCXRACLQFPRCBB-ZWKOTPCHSA-N dihydrocannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)C)CCC(C)=C1 PCXRACLQFPRCBB-ZWKOTPCHSA-N 0.000 claims 1
- 238000004090 dissolution Methods 0.000 claims 1
- 239000012153 distilled water Substances 0.000 claims 1
- 235000013312 flour Nutrition 0.000 claims 1
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- 239000008273 gelatin Substances 0.000 claims 1
- 235000019322 gelatine Nutrition 0.000 claims 1
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- 229920002674 hyaluronan Polymers 0.000 claims 1
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- 150000003904 phospholipids Chemical class 0.000 claims 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
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Claims (27)
1. Препарат с водной липосомной формулой терпена включающей:
первичный терпен, отобранный из группы, включающей α-пинен, α-бизаболол, β-пипен, гуаен, гуайол, лимонен, мирцен и оцимен;
вторичный терпен;
третичный терпен,
где первичный терпен в формуле составляет 50% (процент от массы), вторичный терпен - примерно от 30% до 40% (процент от массы) и третичный терпен - примерно от 8% до 10% (процент от массы).
2. Препарат по п. 1, отличающийся тем, что в формулу дополнительно включены один или несколько каннабиноидов или их аналогов, при среднем диаметре липосомы в формуле в пределах 50-1000 нм.
3. Препарат по п. 2, отличающийся тем, что максимальная конечная концентрация каннабиноидов или их аналогов составляет примерно от 0,01 г/л до 100 г/л.
4. Препарат по п. 2, отличающийся тем, что один или несколько каннабиноидов или их аналогов выбраны из группы в составе каннабинола, каннадибиола, Δ9-тетрагидроканнабинола, Δ8-тетрагидроканнабинола, 11-гидрокси-тетрагидроканнабинола, 11-гидрокси-Δ9-тетрагидро каннабинола, левонантрадола, Δ11-тетрагидроканнабинола, тетрагидроканнабиварина, дронабинола, амандамида и набилона, и комбинации двух или более смесей.
5. Препарат по п. 2, отличающийся тем, что в формулу дополнительно включен стабилизатор, выбранный из группы в составе гуаровой смолы, гиалуроновой кислоты, целлюлозы, ксантановой смолы, поливинилового пирролидона (PVP), альгината, сульфат хондритина, полигаммаглютаминовой кислоты, желатина, хитизина, кукурузного крахмала и муки, в объеме примерно от 0,1% до 2% (процент от объема).
6. Препарат по п. 1, отличающийся тем, что первичный терпен представлен α-пиненом, вторичный терпен выбран из группы в составе мирцена, β-пинена и t-карофиллена, третичный терпен выбран из группы в составе β-пинена, t-карофиллена, α-бизаболола и мирцена, а в суспензию дополнительно входит незначительное количество одного или нескольких терпенов, выбранных из группы в составе α-гумулена, α-бизаболола, гуаена, лимонена, оцимена, терпинолена, 3-карена, миерцена, гуайола, α-терпинеола и
линалоола.
7. Препарат по п. 1, отличающийся тем, что первичный терпен представлен α-бизабололом, а вторичный терпен t-карофилленом, третичный терпен выбран из группы в составе α-пинена и мирцена, а в суспензию дополнительно входит незначительное количество одного или нескольких терпенов, выбранных из группы в составе α-гумулена, α-терпинеола, гуайола и линалоола.
8. Препарат по п. 1, отличающийся тем, что первичный терпен представлен β-пиненом, а вторичный терпен α-пиненом, третичный терпен выбран из группы в составе t-карофиллена и терпинолена, а в суспензию дополнительно входит незначительное количество мирцена.
9. Препарат по п. 1, отличающийся тем, что первичный терпен представлен гуайеном, а вторичный терпен t-карофилленом, третичный терпен выбран из группы в составе мирцена и α-гумулена, а в суспензию дополнительно входит незначительное количество α-пинена, α-бизаболола, β-пинена, лимонена, оцимена и терпинолена.
10. Препарат по п. 1, отличающийся тем, что первичный терпен представлен гуайолом, а вторичный терпен α-бизабололом, третичный терпен выбран из группы в составе t-карофиллена мирцена, а в суспензию дополнительно входит незначительное количество α-пинена, α-терпинеола, α-гумулена и терпинолена.
11. Препарат по п. 1, отличающийся тем, что первичный терпен представлен лимоненом, вторичный терпен выбран из группы в составе мирцена и t-карофиллена, третичный терпен выбран из группы в составе линалоола, мирцена, β-пинена и t-карофиллена, α-бизаболола и мирцена, а в суспензию дополнительно входит незначительное количество одного или нескольких терпенов, выбранных из группы в составе α-гумулена, α-пинена, β-пинена, фенхола, гуайена, линалоола, оцимена и α-терпинеола.
12. Препарат по п. 1, отличающийся тем, что первичный терпен представлен мирценом, вторичный терпен выбран из группы в составе α-пинена, t-карофиллена, терпинолена, оцимена, лимонена и линалоола, третичный терпен выбран из группы в составе β-пинена, t-карофиллена, лимонена, оцимена и мирцена; α-пинена, бизаболола и мирцена, а в суспензию дополнительно входит незначительное количество одного или нескольких терпенов, выбранных из группы в составе α-гумулена, α-бизаболола, гуаена, лимонена, оцимена, 3-карена, β-пинена, α-пинена, миерцена, гуайола, α-терпинеола,
терпинолена и линалоола.
13. Метод приготовления стабильной липосомальной формулы, содержащей один или несколько терпенов, состоит из следующих операций:
(a) растворить один или несколько терпенов в этаноле для получения этанолового раствора терпенов;
(b) добавить фосфолипид в этаноловый раствор терпенов;
(c) произвести впрыск полученного при выполнении операции (b) раствора в дистиллированную воду для получения водно-спиртовой липосомальной формулы терпенов;
(d) извлечь этанол из водно-спиртовой липосомальной формулы терпенов для получения стабильной водной липосомальной формулы с одним или несколькими терпенами, где максимальная конечная концентрация терпенов в липосомальной формуле составляет примерно от 0,01 г/л до 100 г/л.
14. Метод по п. 13, отличающийся тем, что максимальная конечная концентрация терпенов в липосомальной формуле составляет примерно от 10 г/л до 70 г/л.
15. Метод по п. 13, отличающийся тем, что, при выполнении операции (а) дополнительно применяется растворение одного или нескольких каннабиноидов или аналогов каннабиноидов, выбранных из группы в составе каннабинола, каннабидиола, Δ9-тетрагидроканнабинола, Δ8-тетрагидроканнабинола, 11-гидрокси-тетрагидроканнабинола, 11-гидрокси-Δ9-тетрагидроканнабинола, левонантрадола, Δ11-тетрагидроканнабинола, тетрагидроканнабиварина, дронабинола, амандамида, набилона и их сочетаний.
16. Метод по п. 15, отличающийся тем, что средний диаметр липосомов составляет от 50 нм до 1000 нм, а максимальная конечная концентрация каннабиноидов или аналогов каннабиноидов в суспензии - примерно от 0,01 г/л до 100 г/л.
17. Препарат в виде водного раствора терпена и каннабиноида включает в себя первичный терпен, вторичный терпен и третичный терпен, а также один или несколько каннабиноидов или аналогов каннабиноидов, при общем содержании терпена и каннабиноида или терпена и аналога каннабиноида, равном 50 г/л.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11040932B2 (en) | 2018-10-10 | 2021-06-22 | Treehouse Biotech, Inc. | Synthesis of cannabigerol |
US11084770B2 (en) | 2016-12-07 | 2021-08-10 | Treehouse Biotech, Inc. | Cannabis extracts |
US11202771B2 (en) | 2018-01-31 | 2021-12-21 | Treehouse Biotech, Inc. | Hemp powder |
Families Citing this family (124)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10738268B2 (en) * | 2016-08-21 | 2020-08-11 | Insectergy, Llc | Cannabis nanoemulsion methods |
US10595555B2 (en) * | 2013-11-04 | 2020-03-24 | Jason Wasserman | Methods for creating concentrated plant material solutions |
US20160037823A1 (en) * | 2014-08-11 | 2016-02-11 | Aari Ruben | Medical therapy using cigarettes |
MX2017005277A (es) | 2014-10-21 | 2018-01-11 | United Cannabis Corp | Extractos de cannabis y métodos de preparación y uso de la misma. |
US10350165B2 (en) | 2014-12-12 | 2019-07-16 | Ojai Energetics Pbc | Methods and systems for forming stable droplets |
JP2018505912A (ja) * | 2014-12-12 | 2018-03-01 | オーハイ エナジェティクス ピービーシー | マイクロカプセル化カンナビノイド組成物 |
CA3050535C (en) | 2014-12-15 | 2021-11-09 | Richard Clark Kaufman | Methods of treating inflammatory disorders and global inflammation with compositions comprising phospholipid nanoparticle encapsulations of anti-inflammatory nutraceuticals |
EP3261629A4 (en) * | 2015-02-27 | 2018-12-05 | Ebbu, LLC | Compositions comprising combinations of purified cannabinoids, with at least one flavonoid, terpene, or mineral |
BR112017018316A2 (pt) | 2015-02-27 | 2018-04-17 | Ebbu Llc | composições compreendendo combinações de canabinoides purificados, com pelo menos um flavonoide, terpeno ou mineral |
US10383816B2 (en) | 2015-03-02 | 2019-08-20 | Afgin Pharma, Llc | Topical regional neuro-affective therapy with cannabinoid combination products |
CN107530318A (zh) | 2015-03-02 | 2018-01-02 | 阿福金制药有限责任公司 | 用***素的局部区域神经影响性疗法 |
AU2015385825A1 (en) * | 2015-03-10 | 2017-10-05 | Nanosphere Health Sciences, Llc | Lipid nanoparticle compositions and methods as carriers of cannabinoids in standardized precision-metered dosage forms |
AU2016231788A1 (en) * | 2015-03-19 | 2017-10-12 | One World Cannabis Ltd | Preparations of cannabis emulsions and methods thereof |
US9962340B2 (en) | 2015-06-09 | 2018-05-08 | Life Tech Global, Llc | Device and method for the transdermal delivery of cannabidiol |
US10272125B2 (en) * | 2015-09-14 | 2019-04-30 | Life Tech Global, Llc | Transdermal delivery of cannabidiol with other active moieties including cannabinoids |
WO2017051398A1 (en) * | 2015-09-27 | 2017-03-30 | Buzzelet Development And Technologies Ltd. | Methods for the production of different cannabis product compositions |
EP3368033A4 (en) * | 2015-10-31 | 2019-06-26 | Canabuzz-Med | THERAPEUTIC HONEY CANNABINOID COMPOSITION |
US11590230B2 (en) * | 2015-12-07 | 2023-02-28 | Elka Touitou | Compositions of therapeutic substances, methods and uses thereof |
US10328216B2 (en) * | 2016-01-20 | 2019-06-25 | Flurry Powders, Llc | Encapsulation of lipophilic ingredients in dispensible spray dried powders suitable for inhalation |
US11833118B2 (en) | 2016-01-20 | 2023-12-05 | Flurry Powders, Llc | Encapsulation of lipophilic ingredients in dispersible spray dried powders suitable for inhalation |
US11166912B2 (en) * | 2016-03-03 | 2021-11-09 | Ctt Pharma Inc. | Orally administrable composition |
CA3017696A1 (en) * | 2016-03-16 | 2017-09-21 | Buzzelet Development And Technologies Ltd | Terpene-enriched cannabinoid composition |
US10542770B2 (en) | 2016-03-18 | 2020-01-28 | Aceso Wellness LLC | Cannabinoid emulsion product and process for making the same |
CN109069459A (zh) * | 2016-04-12 | 2018-12-21 | 哈比制药私人有限公司 | 脂质体制剂和治疗方法 |
EP3445179A4 (en) * | 2016-04-19 | 2020-07-22 | Canna-B Cure Ltd | ENZYMATICALLY TREATED THERAPEUTIC COMPOSITION ENRICHED IN CANNABIS |
US20190142788A1 (en) * | 2016-05-04 | 2019-05-16 | Inmed Pharmaceuticals Inc. | Use of topical formulations of cannabinoids in the treatment of epidermolysis bullosa and related connective tissue disorders |
EP3452026A4 (en) * | 2016-05-06 | 2019-12-25 | Harvest Direct Enterprises LLC | METHODS OF MANUFACTURE, COMPOSITIONS AND MEDICAL APPLICATIONS OF ORAL-ADDED CANNABIS-BASED PHARMACEUTICAL PRODUCTS |
EP3463304A4 (en) * | 2016-05-24 | 2020-01-08 | Bol Pharma Ltd. | COMPOSITIONS COMPRISING CANNABIDIOL AND HYALURONIC ACID FOR THE TREATMENT OF INFLAMMATORY JOINT DISEASES |
US10499584B2 (en) | 2016-05-27 | 2019-12-10 | New West Genetics | Industrial hemp Cannabis cultivars and seeds with stable cannabinoid profiles |
JP6992057B2 (ja) | 2016-06-10 | 2022-01-13 | クラリティ コスメティックス インコーポレイテッド | 非面皰形成性の毛髪および頭皮ケア製剤ならびにその使用方法 |
JP7454332B2 (ja) * | 2016-06-15 | 2024-03-22 | オーハイ エナジェティクス ピービーシー | 酸化ストレスを低減するための方法および組成物 |
BR112018076283A2 (pt) * | 2016-06-15 | 2019-03-26 | Ojai Energetics Pbc | métodos e composições para potencializar terapias de célula tronco |
IL246790A0 (en) | 2016-07-14 | 2016-09-29 | Friedman Doron | Self-dissolving compounds of cannabinoids |
WO2018017431A1 (en) * | 2016-07-16 | 2018-01-25 | Connoisseur Holdings, Llc | System and method of forming a terpene solution |
WO2018023163A1 (en) | 2016-08-03 | 2018-02-08 | Zelda Therapeutics Operations Pty Ltd | Cannabis composition |
US20180049994A1 (en) | 2016-08-16 | 2018-02-22 | Afgin Pharma, Llc | Topical regional neuro-affective therapy with caryophyllene |
US10568865B2 (en) | 2016-08-29 | 2020-02-25 | Canopy Growth Corporation | Water soluble compositions comprising purified cannabinoids |
WO2018075730A1 (en) * | 2016-10-21 | 2018-04-26 | Axim Biotechnologies, Inc. | Suppositories comprising cannabinoids |
US10857482B1 (en) * | 2016-12-07 | 2020-12-08 | Rien Havens | Botanical super heated processing equipment |
JP7436209B2 (ja) | 2016-12-16 | 2024-02-21 | フレーヴァーセンス | 活性成分を有する乾燥フレーク |
US11974984B2 (en) | 2017-02-09 | 2024-05-07 | Caamtech, Inc. | Compositions and methods comprising a combination of serotonergic drugs |
US20210346346A1 (en) | 2017-02-09 | 2021-11-11 | Caamtech, Inc. | Compositions comprising a serotonergic tryptamine compound |
EP3579832A4 (en) * | 2017-02-09 | 2020-12-30 | Caamtech, LLC | COMPOSITIONS AND PROCESSES INCLUDING A PSILOCYBIN DERIVATIVE |
CN110636834A (zh) * | 2017-02-15 | 2019-12-31 | 分子浸剂有限公司 | 制剂 |
CA3054269A1 (en) * | 2017-03-02 | 2018-09-07 | Iiw Entourage Delivery Systems Ltd | Aromatized and flavored paper products |
EP3600271A4 (en) * | 2017-03-30 | 2020-12-16 | Ojai Energetics PBC | PROCEDURES AND COMPOSITIONS FOR THE IMPROVEMENT OF HEALTH |
WO2018204326A1 (en) * | 2017-05-01 | 2018-11-08 | Mj Wooly Corporation | Methodology and formulation for creating a powder of an encapsulated cannabis-based component embedded in a polymer matrix |
EP3630063A2 (en) | 2017-05-22 | 2020-04-08 | GBS Global Biopharma, Inc. | Myrcene-containing complex mixtures targeting trpv1 |
EP3630067A4 (en) * | 2017-05-26 | 2021-08-11 | Altum Pharmaceuticals Inc. | BIPHASIC CANNABINOID ADMINISTRATION |
US10058531B1 (en) * | 2017-06-01 | 2018-08-28 | Spartak LLC | Dosage delivery film |
US10206888B2 (en) | 2017-06-06 | 2019-02-19 | Cmg Partners, Inc. | Cannabis-based therapeutic product for treatment of chronic pain |
WO2019003163A2 (en) * | 2017-06-28 | 2019-01-03 | Buzzelet Development And Technologies Ltd. | CANNABINOID PRODUCT ENRICHED IN TERPENE GOOD FOR WOMEN'S HEALTH |
CA3070156A1 (en) * | 2017-07-20 | 2019-01-24 | Yissum Research Development Company Of The Hebrew University Of Jerusam Ltd. | Pharmaceutical film compositions for delivery of lipophilic compounds into and/or across the skin |
CA3071497A1 (en) * | 2017-08-13 | 2019-02-21 | Buzzelet Development And Technologies Ltd | Terpene-enriched cannabinoid composition and method of treatment |
US11925652B2 (en) * | 2017-08-13 | 2024-03-12 | Buzzelet Development And Technologies Ltd | Terpene-enriched cannabinoid composition and method of treatment |
WO2019057899A1 (en) * | 2017-09-22 | 2019-03-28 | Lipid Systems Sp. Z.O.O. | AQUEOUS COMPOSITION COMPRISING AT LEAST ONE PHOSHOLIPID AND AT LEAST ONE TERPENE WITH ACIDICITY ACTIVITY AGAINST DEMODEX |
US10220061B1 (en) | 2017-09-26 | 2019-03-05 | Cynthia Denapoli | Method of reducing stress and anxiety in equines |
WO2019075006A1 (en) * | 2017-10-10 | 2019-04-18 | La'au Pono | TREATMENT OF BOTANICAL EXTRACT DRYED BY SPRAYING |
WO2019084679A1 (en) * | 2017-10-30 | 2019-05-09 | Whistler Technologies Corp. | Terpene enrichment methods and systems |
EP3704263A4 (en) * | 2017-10-30 | 2021-08-25 | Endocanna Health, Inc. | GRAPHIC USER INTERFACES FOR DETERMINING PERSONALIZED ENDOCANNABINOID GENOTYPES AND RELATED RECOMMENDATIONS |
WO2019100168A1 (en) * | 2017-11-27 | 2019-05-31 | Enrico BOUCHARD | Method of preparing a cannabis based terpene beverage and beverage thereof |
US20200330378A1 (en) * | 2018-01-03 | 2020-10-22 | Icdpharma Ltd. | Taste-enhanced cannabinoid submicron emulsion syrup compositions |
EP3735240A4 (en) * | 2018-01-03 | 2021-08-18 | ICDPharma Ltd | SOLID SELF-SYSTEMULATING CANNABINOID COMPOSITIONS |
BR102018002843A2 (pt) | 2018-02-09 | 2019-08-27 | Prati Donaduzzi & Cia Ltda | composição farmacêutica e uso da mesma |
US11951086B2 (en) | 2018-04-03 | 2024-04-09 | Pure Green Pharmaceuticals, Inc. | Tablet or composition having n-acyl ethanolamine and cannabinoid |
CN112969452A (zh) * | 2018-04-09 | 2021-06-15 | 艾乐文特科学公司 | 用于治疗动物疼痛的***提取物 |
EP3793542A4 (en) * | 2018-05-14 | 2022-03-30 | Buzzelet Development And Technologies Ltd | TERPENE-ENRICHED CANNABINOID COMPOSITIONS AND THEIR USES IN THE TREATMENT OF INFECTIOUS DISEASES |
WO2019226833A1 (en) * | 2018-05-22 | 2019-11-28 | Gbs Global Biopharma, Inc. | Cannabinoids and/or terpenes for use in trpv1 modulation |
US11252985B1 (en) * | 2018-05-31 | 2022-02-22 | Cannasphere Biotech, LLC. | Dietary supplement compositions including cannabidiol formulations having enhanced bioavailability with sustained time release and enhanced organoleptics, and methods of making same |
WO2019237201A1 (en) * | 2018-06-12 | 2019-12-19 | Paige Growth Technologies Inc. | Devices, systems and methods for multivariable optimization of plant growth and growth of other phototrophic organisms |
US10946308B2 (en) * | 2018-07-12 | 2021-03-16 | Bright Green Corporation | Enzymatic method for extraction and purification of phytocannabinoids |
US10946307B2 (en) * | 2018-07-12 | 2021-03-16 | Bright Green Corporation | Extraction of cannabinoids, curcuminoids and ginsenosides |
US11235013B2 (en) | 2018-09-04 | 2022-02-01 | Babak Ghalili | Cannabinoid, menthol and caffeine dissolvable film compositions, devices and methods |
US11185526B2 (en) | 2018-09-04 | 2021-11-30 | Babak Ghalili | Cannabinoid, menthol and caffeine dissolvable film compositions, devices and methods |
US10695301B2 (en) * | 2018-09-04 | 2020-06-30 | Babak Ghalili | Veterinary cannabinoid and menthol compositions and methods |
US11020355B2 (en) * | 2018-09-06 | 2021-06-01 | NuVessl, Inc. | Method of encapsulating cannabinoids in phospholipid carriers |
CA3115985A1 (en) * | 2018-10-10 | 2020-04-16 | Tilray, Inc. | Methods and formulations for treating chemotherapy-induced nausea and vomiting |
EP3873440A4 (en) * | 2018-11-01 | 2022-08-17 | Molecular Infusions, LLC | POLYMER-BASED ORAL CANNABINOID AND/OR TERPEN FORMULATIONS |
KR20210114409A (ko) * | 2018-12-11 | 2021-09-23 | 디스럽션 랩스 인코퍼레이티드 | 치료제 전달용 조성물과 이의 이용 및 제조 방법 |
EP3897684A4 (en) * | 2018-12-21 | 2022-10-12 | Botaneco Inc. | CANNABINOID FORMULATIONS AND METHODS OF PREPARING THEM |
AU2019412825A1 (en) * | 2018-12-27 | 2021-08-12 | Buzzelet Development And Technologies Ltd. | Herbal preparation-enriched cannabinoid composition and method of treatment |
EP3911148A4 (en) * | 2019-01-17 | 2022-10-12 | Synthonics, Inc. | SOLID MICELLAR COMPOSITIONS OF CANNABINOID ACIDS |
US11154502B2 (en) | 2019-01-24 | 2021-10-26 | CannaClear Inc. | Lecithin vesicles for oral delivery |
CA3038349C (en) * | 2019-01-31 | 2021-04-13 | Nam Hai LAI | Process for producing a nano-cbd liposome system |
CA3127476A1 (en) * | 2019-02-07 | 2020-08-13 | Cannasoul Analytics Ltd. | Cannabinoid containing composition, methods of preparation and use thereof |
WO2020163775A1 (en) * | 2019-02-08 | 2020-08-13 | Srin Therapeutics, Inc. | Cannabinoid compositions and methods of use thereof for immune modulation, immune protection, and treatment of cancer |
CA3130763A1 (en) | 2019-02-25 | 2020-09-03 | Ginkgo Bioworks, Inc. | Biosynthesis of cannabinoids and cannabinoid precursors |
AU2020260090C9 (en) * | 2019-04-15 | 2023-08-31 | Metagenics LLC | Novel hemp and PEA formulation and its use |
US10993928B2 (en) * | 2019-04-26 | 2021-05-04 | Natural Extraction Systems, LLC | Compositions comprising non-crystalline forms of cannabidiol |
CN111838746B (zh) * | 2019-04-30 | 2022-04-05 | 云南汉盟制药有限公司 | 一种香烟爆珠及其制备方法和香烟 |
US11298336B2 (en) | 2019-05-30 | 2022-04-12 | Soluble Technologies, Inc. | Water soluble formulation |
CA3141564A1 (en) * | 2019-06-03 | 2020-12-10 | Benuvia Manufacturing, Llc | Cannabidiol nanocrystal compositions |
KR102478632B1 (ko) * | 2019-06-18 | 2022-12-19 | 바이오메디칼쓰리디프린팅 주식회사 | Cbd를 포함하는 3d 객체 및 그의 프린팅 운영 시스템 |
US20220242050A1 (en) * | 2019-06-18 | 2022-08-04 | Bio Medical 3D Printing Co., Ltd. | 3d object containing cbd and printing operating system therefor |
US11622956B1 (en) * | 2019-06-26 | 2023-04-11 | RCR BioPharma | Compound and method for treating diseases and disorders |
WO2021003091A1 (en) * | 2019-07-03 | 2021-01-07 | Vertosa Inc. | Infusion of emulsified hydrophobic active ingredients into high polyphenolic beverages |
US20210023005A1 (en) * | 2019-07-26 | 2021-01-28 | Landsteiner Scientific S.A. De C.V. | Cannabinoid-containing compositions in the form of spheres or sphere-like particles, methods for their preparation, and therapeutic applications |
WO2021064730A1 (en) * | 2019-10-03 | 2021-04-08 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd | Liposomal cannabinoids and uses thereof |
GB2588172B (en) * | 2019-10-11 | 2023-05-24 | Blackhawk Partners Ltd | A pharmaceutical composition comprising cannabinoid |
US20220401381A1 (en) * | 2019-11-08 | 2022-12-22 | Vella Bioscience, Inc. | Peripherally acting cannabidiol (cbd)-containing compounds and uses thereof for enhancing female sexual function or treating female sexual disorders |
CA3171272A1 (en) * | 2020-03-09 | 2021-09-16 | Gregory S. Baldi | Process for making a water soluble, full spectrum hemp oil |
WO2021179087A1 (en) * | 2020-03-11 | 2021-09-16 | Hexo Operations Inc. | Terpene-enhanced compositions and uses thereof |
WO2021179088A1 (en) * | 2020-03-13 | 2021-09-16 | Hexo Operations Inc. | Terpene-enhanced compositions and uses thereof |
BR112022023352A2 (pt) * | 2020-05-18 | 2023-05-02 | Max Biology Co Ltd | Composições, método para fornecer um agente bioativo, preparar uma pluralidade de partículas compósitas, tratar doença do olho seco e tratar uma doença ou afecção e método de uso recreativo |
FR3110427B1 (fr) * | 2020-05-20 | 2023-07-14 | Laboratoires Eriger | Conjugué terpenique de couplage |
CN113925896A (zh) * | 2020-06-29 | 2022-01-14 | 汉义生物科技(北京)有限公司 | 一种含***提取物的药物组合物、制剂及其应用 |
US11786475B2 (en) | 2020-07-22 | 2023-10-17 | Soluble Technologies Inc. | Film-based dosage form |
CN111643377B (zh) * | 2020-07-23 | 2023-08-11 | 中国热带农业科学院南亚热带作物研究所 | 一种汉麻油纳米微胶囊及其制备方法和应用 |
EP4188363A1 (en) | 2020-07-28 | 2023-06-07 | Wsmef, Llc | Micelle preparations of full-spectrum hemp oil for treating type ii diabetes, reducing inflammation during covid-19, and improving sleep quality |
WO2022027053A1 (en) * | 2020-07-28 | 2022-02-03 | Wsmef, Llc | Micelle preparations of full-spectrum hemp oil for treating type ii diabetes, reducing inflammation during covid-19, and improving sleep quality |
US20220054446A1 (en) * | 2020-08-18 | 2022-02-24 | Yvette Rose Webb | Targeted treatment with a topical cream of cannabinoids, terpenes, and essential oils |
US11731950B2 (en) * | 2020-09-07 | 2023-08-22 | Shuang Xie | Mass production and application of Δ 8 THC |
AU2021376539A1 (en) * | 2020-11-06 | 2023-06-15 | Zelira Therapeutics Operations Pty Ltd | Cannabinoid encapsulation technology |
WO2022126112A1 (en) * | 2020-12-08 | 2022-06-16 | Dt Ip Holdings I, Llc | Formulations containing cannabinoids |
CA3204862A1 (en) | 2020-12-09 | 2022-06-16 | I+Med S. Coop. | Composition comprising sea water and cannabinoid loaded submicroparticles for pharmaceutical, nutraceutical and cosmetic applications |
CN112472661A (zh) * | 2020-12-11 | 2021-03-12 | 云南苏旺润生物医药有限公司 | 一种***二酚按摩油组合物及其制备方法和应用 |
CA3102947A1 (en) * | 2020-12-18 | 2022-06-18 | Skymount Medical Us Inc. | Nutraceuticals useful in the treatment of coronavirus diseases |
US20240049760A1 (en) * | 2020-12-24 | 2024-02-15 | Petro Pawlo Czupiel | Safe-to-ingest microemulsions and nanoemulsions containing lipophilic components |
WO2022140849A1 (en) * | 2021-01-04 | 2022-07-07 | Hexo Operations Inc. | Cannabinoid compositions with taste-barrier properties |
WO2022165165A1 (en) * | 2021-01-29 | 2022-08-04 | The Johns Hopkins University | Limonene effects on tetrahydrocannabinol (thc)-induced anxiety |
US12011470B2 (en) | 2021-07-28 | 2024-06-18 | Clint Sorensen | Micelle preparations of full-spectrum hemp oil |
WO2023060323A1 (en) * | 2021-10-15 | 2023-04-20 | Bod Science Limited | Terpene-containing formulations and use thereof |
WO2023212170A1 (en) * | 2022-04-29 | 2023-11-02 | Abstrax Tech Inc. | Endogenous stabilization of cannabinoids |
WO2024057304A1 (en) * | 2022-09-12 | 2024-03-21 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Compositions for dermal/transdermal delivery and cosmetic use |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0927025A4 (en) * | 1996-09-18 | 2001-07-25 | Dragoco Inc | DRY POWDER COMPOSITION WITH ACTIVE INGREDIENT ENCLOSED IN LIPOSOMES |
US20030180349A1 (en) * | 2001-12-07 | 2003-09-25 | Franklin Lanny U. | Respiratory infection prevention and treatment with terpene-containing compositions |
GB0202385D0 (en) * | 2002-02-01 | 2002-03-20 | Gw Pharma Ltd | Compositions for the treatment of nausea,vomiting,emesis,motion sicknes or like conditions |
CA2659775A1 (en) * | 2006-08-04 | 2008-02-14 | Insys Therapeutics Inc. | Aqueous dronabinol formulations |
EP2201942A1 (de) * | 2008-12-23 | 2010-06-30 | Intendis GmbH | Zusammensetzung mit Hanföl für die Behandlung topischer Erkrankungen |
GB2478595B (en) * | 2010-03-12 | 2018-04-04 | Gw Pharma Ltd | Phytocannabinoids in the treatment of glioma |
GB2479153B (en) * | 2010-03-30 | 2014-03-19 | Gw Pharma Ltd | The phytocannabinoid cannabidivarin (CBDV) for use in the treatment of epilepsy |
WO2013009928A1 (en) * | 2011-07-11 | 2013-01-17 | Organic Medical Research | Cannabinoid formulations |
-
2014
- 2014-10-31 RU RU2016129536A patent/RU2016129536A/ru not_active Application Discontinuation
- 2014-10-31 US US15/033,023 patent/US20160279073A1/en not_active Abandoned
- 2014-10-31 KR KR1020167014451A patent/KR20160094950A/ko not_active Application Discontinuation
- 2014-10-31 CA CA2929280A patent/CA2929280A1/en not_active Abandoned
- 2014-10-31 WO PCT/IB2014/003156 patent/WO2015068052A2/en active Application Filing
- 2014-10-31 EP EP14851442.5A patent/EP3062774A2/en not_active Withdrawn
- 2014-10-31 AU AU2014347807A patent/AU2014347807A1/en not_active Abandoned
- 2014-10-31 JP JP2016551089A patent/JP2016537412A/ja active Pending
- 2014-10-31 CN CN201480068135.XA patent/CN105916492A/zh active Pending
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2016
- 2016-05-01 IL IL245368A patent/IL245368A0/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11084770B2 (en) | 2016-12-07 | 2021-08-10 | Treehouse Biotech, Inc. | Cannabis extracts |
US11202771B2 (en) | 2018-01-31 | 2021-12-21 | Treehouse Biotech, Inc. | Hemp powder |
US11040932B2 (en) | 2018-10-10 | 2021-06-22 | Treehouse Biotech, Inc. | Synthesis of cannabigerol |
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JP2016537412A (ja) | 2016-12-01 |
CN105916492A (zh) | 2016-08-31 |
IL245368A0 (en) | 2016-06-30 |
WO2015068052A2 (en) | 2015-05-14 |
EP3062774A2 (en) | 2016-09-07 |
KR20160094950A (ko) | 2016-08-10 |
CA2929280A1 (en) | 2015-05-14 |
WO2015068052A3 (en) | 2015-09-03 |
US20160279073A1 (en) | 2016-09-29 |
AU2014347807A1 (en) | 2016-05-26 |
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