(1S,4S,5S,7aR)-5-ethenyl-1,4,5,7a-tetramethyl-2,4,6,7-tetrahydro-1H-indene

Details

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Internal ID 1e35591e-0019-4c8b-8869-28d3d36ae767
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name (1S,4S,5S,7aR)-5-ethenyl-1,4,5,7a-tetramethyl-2,4,6,7-tetrahydro-1H-indene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-6-14(4)9-10-15(5)11(2)7-8-13(15)12(14)3/h6,8,11-12H,1,7,9-10H2,2-5H3/t11-,12+,14+,15+/m0/s1
InChI Key WWXVUFOHSHXMKJ-CTHBEMJXSA-N
Popularity 0 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 5.00
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 (1S,4S,5S,7aR)-5-ethenyl-1,4,5,7a-tetramethyl-2,4,6,7-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 + 0.9928 99.28%
Caco-2 + 0.7693 76.93%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.7991 79.91%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9490 94.90%
OATP1B3 inhibitior + 0.8943 89.43%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9394 93.94%
P-glycoprotein inhibitior - 0.9441 94.41%
P-glycoprotein substrate - 0.9135 91.35%
CYP3A4 substrate - 0.5179 51.79%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.8435 84.35%
CYP2C9 inhibition - 0.7701 77.01%
CYP2C19 inhibition - 0.7161 71.61%
CYP2D6 inhibition - 0.9405 94.05%
CYP1A2 inhibition - 0.7411 74.11%
CYP2C8 inhibition - 0.8391 83.91%
CYP inhibitory promiscuity - 0.6652 66.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Warning 0.4672 46.72%
Eye corrosion - 0.9392 93.92%
Eye irritation + 0.5771 57.71%
Skin irritation - 0.5154 51.54%
Skin corrosion - 0.9786 97.86%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6671 66.71%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5591 55.91%
skin sensitisation + 0.8108 81.08%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6418 64.18%
Acute Oral Toxicity (c) III 0.7477 74.77%
Estrogen receptor binding - 0.8917 89.17%
Androgen receptor binding - 0.6039 60.39%
Thyroid receptor binding - 0.5580 55.80%
Glucocorticoid receptor binding - 0.7948 79.48%
Aromatase binding - 0.5844 58.44%
PPAR gamma - 0.8650 86.50%
Honey bee toxicity - 0.8382 83.82%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7200 72.00%
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
CHEMBL3492 P49721 Proteasome Macropain subunit 90.57% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.60% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.37% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.94% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.57% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.60% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.75% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163047709
LOTUS LTS0003026
wikiData Q105314416