(2S,3S,3aS,4R,7aS)-6-ethenyl-3,3a,7,7a-tetramethyl-2,3,4,5-tetrahydro-1H-indene-2,4-diol

Details

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Internal ID 4ebe841e-6317-41ee-96df-af6cdf2896fa
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name (2S,3S,3aS,4R,7aS)-6-ethenyl-3,3a,7,7a-tetramethyl-2,3,4,5-tetrahydro-1H-indene-2,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-6-11-7-13(17)15(5)10(3)12(16)8-14(15,4)9(11)2/h6,10,12-13,16-17H,1,7-8H2,2-5H3/t10-,12+,13-,14+,15-/m1/s1
InChI Key PDROKIQEFJBKSQ-MYBUGEPTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S,3aS,4R,7aS)-6-ethenyl-3,3a,7,7a-tetramethyl-2,3,4,5-tetrahydro-1H-indene-2,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.6994 69.94%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.7128 71.28%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9118 91.18%
OATP1B3 inhibitior + 0.9160 91.60%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9082 90.82%
P-glycoprotein inhibitior - 0.9532 95.32%
P-glycoprotein substrate - 0.8355 83.55%
CYP3A4 substrate + 0.5173 51.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7337 73.37%
CYP3A4 inhibition - 0.7612 76.12%
CYP2C9 inhibition - 0.9081 90.81%
CYP2C19 inhibition - 0.8061 80.61%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.7380 73.80%
CYP2C8 inhibition - 0.9381 93.81%
CYP inhibitory promiscuity - 0.7526 75.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7937 79.37%
Carcinogenicity (trinary) Non-required 0.5345 53.45%
Eye corrosion - 0.9835 98.35%
Eye irritation - 0.8701 87.01%
Skin irritation + 0.6302 63.02%
Skin corrosion - 0.9165 91.65%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5108 51.08%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5249 52.49%
skin sensitisation + 0.6322 63.22%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.7163 71.63%
Acute Oral Toxicity (c) III 0.7132 71.32%
Estrogen receptor binding - 0.7882 78.82%
Androgen receptor binding - 0.5297 52.97%
Thyroid receptor binding - 0.7117 71.17%
Glucocorticoid receptor binding - 0.8198 81.98%
Aromatase binding - 0.6620 66.20%
PPAR gamma - 0.7550 75.50%
Honey bee toxicity - 0.8417 84.17%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9629 96.29%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.43% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.64% 85.14%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.29% 86.00%
CHEMBL1951 P21397 Monoamine oxidase A 84.58% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.36% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.90% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.36% 100.00%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.63% 95.58%
CHEMBL240 Q12809 HERG 80.11% 89.76%

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.
Porella platyphylla

Cross-Links

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PubChem 163062485
LOTUS LTS0258309
wikiData Q105206708