(6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydrobenzo[c]chromene-1,2-diol

Details

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Internal ID 9e76909f-4f3c-4377-9ee3-780d0bca05c3
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name (6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydrobenzo[c]chromene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O3/c1-5-6-7-8-14-12-17-18(20(23)19(14)22)15-11-13(2)9-10-16(15)21(3,4)24-17/h11-12,15-16,22-23H,5-10H2,1-4H3/t15-,16-/m1/s1
InChI Key XXGMIHXASFDFSM-HZPDHXFCSA-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 6.60
Atomic LogP (AlogP) 5.44
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydrobenzo[c]chromene-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9868 98.68%
Caco-2 + 0.7696 76.96%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6837 68.37%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8299 82.99%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4939 49.39%
P-glycoprotein inhibitior - 0.6161 61.61%
P-glycoprotein substrate - 0.6620 66.20%
CYP3A4 substrate + 0.6880 68.80%
CYP2C9 substrate - 0.6031 60.31%
CYP2D6 substrate + 0.4351 43.51%
CYP3A4 inhibition - 0.6793 67.93%
CYP2C9 inhibition + 0.6173 61.73%
CYP2C19 inhibition + 0.6985 69.85%
CYP2D6 inhibition - 0.7836 78.36%
CYP1A2 inhibition + 0.6261 62.61%
CYP2C8 inhibition + 0.8141 81.41%
CYP inhibitory promiscuity + 0.7322 73.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6784 67.84%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9025 90.25%
Skin irritation - 0.6961 69.61%
Skin corrosion - 0.9076 90.76%
Ames mutagenesis - 0.7691 76.91%
Human Ether-a-go-go-Related Gene inhibition - 0.3605 36.05%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation - 0.6782 67.82%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8383 83.83%
Acute Oral Toxicity (c) III 0.6529 65.29%
Estrogen receptor binding + 0.6705 67.05%
Androgen receptor binding + 0.7543 75.43%
Thyroid receptor binding + 0.7339 73.39%
Glucocorticoid receptor binding + 0.8833 88.33%
Aromatase binding + 0.7769 77.69%
PPAR gamma + 0.8409 84.09%
Honey bee toxicity - 0.9224 92.24%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6275 62.75%
Fish aquatic toxicity + 0.9955 99.55%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.61% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.88% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 97.37% 89.63%
CHEMBL2581 P07339 Cathepsin D 94.33% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.67% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 91.57% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.62% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.84% 92.94%
CHEMBL2996 Q05655 Protein kinase C delta 88.84% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.69% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.57% 100.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 87.26% 96.25%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.21% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.93% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.63% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.91% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.98% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.52% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.29% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.12% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.91% 92.62%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 81.58% 95.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.17% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.56% 91.71%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.48% 95.17%
CHEMBL4581 P52732 Kinesin-like protein 1 80.38% 93.18%

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 162953051
LOTUS LTS0177909
wikiData Q105344013