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

Details

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Internal ID 4ee68a5f-a5b5-40fd-bcf3-54062122f29e
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (3aS,4R,5R,7aS)-3a,4,5,7a-tetramethyl-2,3-dimethylidene-4,5,6,7-tetrahydro-1H-indene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-10-7-8-14(5)9-11(2)13(4)15(14,6)12(10)3/h10,12H,2,4,7-9H2,1,3,5-6H3/t10-,12-,14+,15-/m1/s1
InChI Key HWUPIPCEJJWJBV-WAZAZEMKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.8735 87.35%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.8102 81.02%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9356 93.56%
OATP1B3 inhibitior + 0.8766 87.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9225 92.25%
P-glycoprotein inhibitior - 0.9151 91.51%
P-glycoprotein substrate - 0.8680 86.80%
CYP3A4 substrate + 0.5164 51.64%
CYP2C9 substrate - 0.8001 80.01%
CYP2D6 substrate - 0.7763 77.63%
CYP3A4 inhibition - 0.7107 71.07%
CYP2C9 inhibition - 0.8314 83.14%
CYP2C19 inhibition - 0.7292 72.92%
CYP2D6 inhibition - 0.9315 93.15%
CYP1A2 inhibition - 0.7026 70.26%
CYP2C8 inhibition - 0.8548 85.48%
CYP inhibitory promiscuity - 0.6100 61.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Warning 0.4673 46.73%
Eye corrosion - 0.9334 93.34%
Eye irritation + 0.7237 72.37%
Skin irritation + 0.5546 55.46%
Skin corrosion - 0.9721 97.21%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5993 59.93%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7022 70.22%
skin sensitisation + 0.8480 84.80%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5923 59.23%
Acute Oral Toxicity (c) III 0.7844 78.44%
Estrogen receptor binding - 0.7509 75.09%
Androgen receptor binding - 0.6394 63.94%
Thyroid receptor binding - 0.7173 71.73%
Glucocorticoid receptor binding - 0.8346 83.46%
Aromatase binding - 0.7126 71.26%
PPAR gamma - 0.7650 76.50%
Honey bee toxicity - 0.8912 89.12%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.78% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.43% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.52% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.17% 92.94%
CHEMBL221 P23219 Cyclooxygenase-1 82.26% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.49% 100.00%
CHEMBL1871 P10275 Androgen Receptor 81.47% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.15% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.04% 86.00%

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.
Ligusticum grayi

Cross-Links

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PubChem 162879833
LOTUS LTS0113185
wikiData Q105034835