(3S,3aS,6S,7Z,7aR)-3,6-dimethyl-7-(2-methylprop-2-enylidene)-1,2,3,3a,4,5,6,7a-octahydroindene

Details

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Internal ID e5f5d37d-ceec-4055-a284-47fe394b1f8f
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (3S,3aS,6S,7Z,7aR)-3,6-dimethyl-7-(2-methylprop-2-enylidene)-1,2,3,3a,4,5,6,7a-octahydroindene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-10(2)9-15-12(4)5-7-13-11(3)6-8-14(13)15/h9,11-14H,1,5-8H2,2-4H3/b15-9-/t11-,12-,13-,14+/m0/s1
InChI Key LOWXYGTWKXWTGY-KBJJDSDRSA-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 5.40
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,3aS,6S,7Z,7aR)-3,6-dimethyl-7-(2-methylprop-2-enylidene)-1,2,3,3a,4,5,6,7a-octahydroindene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9151 91.51%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.7534 75.34%
OATP2B1 inhibitior - 0.8444 84.44%
OATP1B1 inhibitior + 0.9252 92.52%
OATP1B3 inhibitior + 0.8954 89.54%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9075 90.75%
P-glycoprotein inhibitior - 0.9381 93.81%
P-glycoprotein substrate - 0.9197 91.97%
CYP3A4 substrate - 0.5703 57.03%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7357 73.57%
CYP3A4 inhibition - 0.8823 88.23%
CYP2C9 inhibition - 0.8368 83.68%
CYP2C19 inhibition - 0.7481 74.81%
CYP2D6 inhibition - 0.9383 93.83%
CYP1A2 inhibition - 0.5895 58.95%
CYP2C8 inhibition - 0.7514 75.14%
CYP inhibitory promiscuity - 0.6332 63.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Warning 0.4700 47.00%
Eye corrosion - 0.8556 85.56%
Eye irritation - 0.5335 53.35%
Skin irritation + 0.6050 60.50%
Skin corrosion - 0.9758 97.58%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6697 66.97%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8807 88.07%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7971 79.71%
Acute Oral Toxicity (c) III 0.6376 63.76%
Estrogen receptor binding - 0.9121 91.21%
Androgen receptor binding - 0.5166 51.66%
Thyroid receptor binding - 0.5399 53.99%
Glucocorticoid receptor binding - 0.8251 82.51%
Aromatase binding - 0.8463 84.63%
PPAR gamma - 0.8270 82.70%
Honey bee toxicity - 0.8306 83.06%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5700 57.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.05% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.11% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.63% 99.18%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.28% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 80.97% 97.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.83% 92.94%

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.
Frullania tamarisci

Cross-Links

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PubChem 12051854
LOTUS LTS0139063
wikiData Q105154965