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(6aR)-6aβ,7,8,10aα-テトラヒドロ-6,6,9-トリメチル-3-プロピル-6H-ジベンゾ[b,d]ピラン-1-オール

Tetrahydrocannabivarin

HCID 93147
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
31262-37-0
標準SMILES
CCCc1cc(O)c2c(c1)OC(C)(C)[C@@H]1CCC(C)=C[C@@H]21
InChIKey
ZROLHBHDLIHEMS-HUUCEWRRSA-N
分子式
C19H26O2
平均分子量
286.4 g/mol
単同位体質量
286.19328007

概要

Tetrahydrocannabivarin (THCV) is a propyl analogue of tetrahydrocannabinol (Δ9-THC), one of the primary pharmacological components of [Medical Cannabis]. Δ9-THC is currently available in several synthetic forms, including [Dronabinol], while purified or isolated THCV is not approved for any medical uses and is not available as any marketed products. As a major phytocannabinoid, however, THCV is accessible within [Medical Cannabis] along with other identified cannabinoids including [Cannabidiol] (CBD), [cannabinol] (CBN), [cannabigerol] (CBG), [cannabichromene] (CBC), [cannabivarin] (CBV), and [Cannabidivarin] (CBDV). THCV is one of four cannabinoids with identified potential as anticonvulsant agents, which also includes Δ9-tetrahydrocannabinolic acid, [Cannabidiol] (CBD), and [Cannabidivarin] (CBDV). Although THCV possesses an almost identical structure to Δ9-THC (varying only by the length of its lipophilic alkyl chain), it has different molecular targets and pharmacological profile. Compared to THC which demonstrates its effects through weak partial agonist activity of both endocannabinoid receptors Cannabinoid-1 (CB1R) and Cannabinoid-2 (CB2R), THCV acts as a CB1 antagonist and a partial agonist of CB2. Further evidence has also shown that THCV acts as an agonist of GPR55 and l-α-lysophosphatidylinositol (LPI). Beyond the endocannabinoid system, THCV has also been reported to activate 5HT1A receptors to produce an antipsychotic effect that has therapeutic potential for ameliorating some of the negative, cognitive and positive symptoms of schizophrenia. Furthermore, THCV interacts with different transient receptor potential (TRP) channels including TRPV2, which may contribute to the analgesic, anti-inflammatory and anti-cancer effects of cannabinoids and Cannabis extracts. It has also shown antiepileptiform and anticonvulsant properties, that suggest possible therapeutic application in the treatment of pathophysiologic hyperexcitability states such as untreatable epilepsy. Cannabinoid receptors are utilized endogenously by the body through the endocannabinoid system, which includes a group of lipid proteins, enzymes, and receptors that are involved in many physiological processes. Through its modulation of neurotransmitter release, the endocannabinoid system regulates cognition, pain sensation, appetite, memory, sleep, immune function, and mood among many others. These effects are largely mediated through two members of the G-protein coupled receptor family, cannabinoid receptors 1 and 2 (CB1 and CB2). CB1 receptors are found in both the central and peripheral nervous systems, with the majority of receptors localized to the hippocampus and amygdala of the brain. Physiological effects of using cannabis make sense in the context of its receptor activity as the hippocampus and amygdala are primarily involved with regulation of memory, fear, and emotion. In contrast, CB2 receptors are mainly found peripherally in immune cells, lymphoid tissue, and peripheral nerve terminals. Reliably studying the effects of Cannabis (and of THCV) is complicated by the numerous other compounds that Cannabis contains such as terpenes, flavonoids, phenols, amino acids, and fatty acids among many others that have the potential to modulate the plant's pharmacological effect.

名称と識別子

優先名称
Tetrahydrocannabivarin
IUPAC
(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydrobenzo[c]chromen-1-ol
現地名
(6aR)-6aβ,7,8,10aα-テトラヒドロ-6,6,9-トリメチル-3-プロピル-6H-ジベンゾ[b,d]ピラン-1-オール
英語名
Delta9-tetrahydrocannabivarin
分子式
C19H26O2
分子量
286.41

名称と別名

TETRAHYDROCANNABIVARIN31262-37-0delta9-TetrahydrocannabivarinTHCVTHC-V.delta.9-Tetrahydrocannabivarin(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydrobenzo[c]chromen-1-olGWP42004GWP-42004I5YE3I47D8O-4394Cannabivarol, .delta.9-tetrahydro-
名称をさらに表示
[6aR,(-)]-6aβ,7,8,10aα-テトラヒドロ-6,6,9-トリメチル-3-プロピル-6H-ジベンゾ[b,d]ピラン-1-オール(6aR)-3-プロピル-6,6,9-トリメチル-6aβ,7,8,10aα-テトラヒドロ-6H-ジベンゾ[b,d]ピラン-1-オールΔ9-テトラヒドロカンナビバロールΔ9-テトラヒドロカンナビバリンΔ1-テトラヒドロカンナビジバロール(6aR)-6aβ,7,8,10aα-テトラヒドロ-6,6,9-トリメチル-3-プロピル-6H-ジベンゾ[b,d]ピラン-1-オールΔ9-trans-テトラヒドロカンナビバリン(6aR,10aR)-6,6,9-トリメチル-3-プロピル-6H,6aH,7H,8H,10aH-ベンゾ[c]イソクロメン-1-オールΔ9-TetrahydrocannabivarinTetrahydrocannavarinΔ9-TetrahydrocannabivarolΔ1-TetrahydrocannabidivarolTetrahydrocannabivarin(THCV)Tetrahydrocannabivarin (CRM)

物性

構造計算による物性

XLogP
5.9
極性表面積
29.5 Ų
水素結合供与体数
1
水素結合受容体数
2
回転可能結合数
2
重原子数
21
形式電荷
0
複雑度
412

実験および物理化学的性質

Drugs · 2 件

DEA NFLIS-Drug Category -> Cannabinoids

Pharmaceuticals -> Listed in ZINC15

Endocrine DisruptorsPotential endocrine disrupting compound

物理化学的性質

沸点
360.6 · 360.6±42.0 °C(Predicted)
比重(密度)
1.034 · 1.034±0.06 g/cm3(Predicted)
溶解性
10 mg/ml · Methanol: 10 mg/ml
酸解離定数(Pka)
9.79 · 9.79±0.60(Predicted)
InChI
InChI=1S/C19H26O2/c1-5-6-13-10-16(20)18-14-9-12(2)7-8-15(14)19(3,4)21-17(18)11-13/h9-11,14-15,20H,5-8H2,1-4H3/t14-,15-/m1/s1
InChIKey
ZROLHBHDLIHEMS-HUUCEWRRSA-N
SMILES
C12=CC(CCC)=CC(O)=C1[C@]1([H])C=C(C)CC[C@@]1([H])C(C)(C)O2

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 4 件

Warning

H400 (100%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]

P273, P391, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 38 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Hazard Classes and CategoriesAquatic Acute 1 (100%)

安全データ

危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード H410

化学と産業

薬理情報

Pharmacodynamics · 1 件

Compared to THC which demonstrates its effects through weak partial agonist activity at Cannabinoid-1 (CB1R) and Cannabinoid-2 (CB2R) receptors, THCV acts as a CB1 antagonist and a partial agonist of CB2. Further evidence has also shown that THCV acts as an agonist of GPR55 and l-α-lysophosphatidylinositol (LPI). Beyond the endocannabinoid system, THCV has also been reported to activate 5HT1A receptors to produce an antipsychotic effect that has therapeutic potential for ameliorating some of the negative, cognitive and positive symptoms of schizophrenia. Furthermore, THCV interacts with different transient receptor potential (TRP) channels including TRPV1, which may contribute to the analgesic, anti-inflammatory and anti-cancer effects of cannabinoids and Cannabis extracts.

応用分野

説明Tetrahydrocannabivarin (CRM) (Item No. 18091) is a certified reference material categorized as a phytocannabinoid. This product is intended for research and forensic applications.

上流・下流製品情報

上流原料

6H-Dibenzo[b,d]pyran-1-ol, 6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-propyl-, 1-(4-methylbenzenesulfonate), (6aR,10aR)-2-[(1R,6R)-3-メチル-6-(1-メチルエテニル)-2-シクロヘキセン-1-イル]-5-プロピル-1,3-ベンゼンジオール

サプライヤー19 社

广州佳途科技股份有限公司

関連反応

0 件
反応記録を作成

現在のフィルター条件では反応記録がありません。

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
Δ9-trans-Tetrahydrocannabivarin
(-)-.delta.9-trans-Tetrahydrocannabivarin(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydro-6H-dibenzo[b,d]pyran-1-ol6H-Dibenzo(b,d)pyran-1-ol, 6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-propyl-, (6aR-trans)-6H-Dibenzo[b,d]pyran-1-ol, 6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-propyl-, (6aR-trans)-UNII-I5YE3I47D86H-DIBENZO(B,D)PYRAN-1-OL, 6A,7,8,10A-TETRAHYDRO-6,6,9-TRIMETHYL-3-PROPYL-, (6AR,10AR)-6H-Dibenzo[b,d]pyran-1-ol, 6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-propyl-, (6aR,10aR)-

データベース識別子

CAS
31262-37-0
PubChem CID
93147
DTXSID
DTXSID10893920
ChEMBL
CHEMBL2387541
UNII
I5YE3I47D8
EC Number
809-026-4
Nikkaji
J108.077F
81960175-877 18933936954 · [email protected]
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