(6aR,10R,10aR)-6,6-dimethyl-9-methylidene-3-pentyl-7,8,10,10a-tetrahydro-6aH-benzo(c)chromene-1,10-diol

Details

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Internal ID 759e4d2a-eae0-4203-93d3-ae34a740080c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name (6aR,10R,10aR)-6,6-dimethyl-9-methylidene-3-pentyl-7,8,10,10a-tetrahydro-6aH-benzo[c]chromene-1,10-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O3/c1-5-6-7-8-14-11-16(22)19-17(12-14)24-21(3,4)15-10-9-13(2)20(23)18(15)19/h11-12,15,18,20,22-23H,2,5-10H2,1,3-4H3/t15-,18-,20+/m1/s1
InChI Key HDNJNVPZXVJOMB-ZTNFWEORSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O3
Molecular Weight 330.50 g/mol
Exact Mass 330.21949481 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.71
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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(6aR,10R,10aR)-6,6-dimethyl-9-methylidene-3-pentyl-7,8,10,10a-tetrahydro-6aH-benzo(c)chromene-1,10-diol
10alpha-hydroxy-exo-THC
56986-42-6
CHEMBL3586108
10alpha-Hydroxy-delta9'11-hexahydrocannabinol
10-Hydroxy-exo-THC
10|A-Hydroxy-exo-THC
SCHEMBL31545467
DTXSID301357316
BDBM50092345
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (6aR,10R,10aR)-6,6-dimethyl-9-methylidene-3-pentyl-7,8,10,10a-tetrahydro-6aH-benzo(c)chromene-1,10-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.6579 65.79%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6428 64.28%
OATP2B1 inhibitior - 0.7215 72.15%
OATP1B1 inhibitior + 0.8209 82.09%
OATP1B3 inhibitior + 0.9244 92.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7972 79.72%
P-glycoprotein inhibitior - 0.6474 64.74%
P-glycoprotein substrate - 0.5627 56.27%
CYP3A4 substrate + 0.6874 68.74%
CYP2C9 substrate - 0.7786 77.86%
CYP2D6 substrate + 0.5000 50.00%
CYP3A4 inhibition - 0.5091 50.91%
CYP2C9 inhibition + 0.6261 62.61%
CYP2C19 inhibition + 0.7340 73.40%
CYP2D6 inhibition - 0.7819 78.19%
CYP1A2 inhibition + 0.7057 70.57%
CYP2C8 inhibition + 0.7805 78.05%
CYP inhibitory promiscuity + 0.8548 85.48%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7004 70.04%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9643 96.43%
Skin irritation - 0.7127 71.27%
Skin corrosion - 0.9057 90.57%
Ames mutagenesis - 0.7937 79.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6533 65.33%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation - 0.6369 63.69%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6962 69.62%
Acute Oral Toxicity (c) III 0.6514 65.14%
Estrogen receptor binding + 0.6452 64.52%
Androgen receptor binding + 0.7135 71.35%
Thyroid receptor binding + 0.7419 74.19%
Glucocorticoid receptor binding + 0.7721 77.21%
Aromatase binding + 0.7833 78.33%
PPAR gamma + 0.8276 82.76%
Honey bee toxicity - 0.9101 91.01%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6747 67.47%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL218 P21554 Cannabinoid CB1 receptor 117 nM
Ki
via Super-PRED
CHEMBL253 P34972 Cannabinoid CB2 receptor 129 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.88% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.77% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.94% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.07% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.17% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.91% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.69% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.15% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.06% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.03% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.97% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.83% 92.62%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.73% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.30% 92.08%
CHEMBL233 P35372 Mu opioid receptor 85.25% 97.93%
CHEMBL226 P30542 Adenosine A1 receptor 84.52% 95.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.35% 89.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.40% 99.18%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.67% 93.40%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.51% 95.89%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 81.35% 80.33%
CHEMBL3401 O75469 Pregnane X receptor 80.47% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Cannabis sativa

Cross-Links

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PubChem 122180086
LOTUS LTS0090874
wikiData Q105246034