3,5,5-Trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,6-hexahydroindene

Details

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Internal ID 3ce8b083-207a-434f-8334-c15ad9c87ff1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,5,5-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,6-hexahydroindene
SMILES (Canonical) CC1CCC2=C(CC(CC12)(C)C)C(=C)C
SMILES (Isomeric) CC1CCC2=C(CC(CC12)(C)C)C(=C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-15(4,5)9-14-11(3)6-7-12(13)14/h11,14H,1,6-9H2,2-5H3
InChI Key KUBSAWBFAOYMLQ-UHFFFAOYSA-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 4.80
Atomic LogP (AlogP) 4.73
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 3,5,5-Trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,6-hexahydroindene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8427 84.27%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.7438 74.38%
OATP2B1 inhibitior - 0.8469 84.69%
OATP1B1 inhibitior + 0.9005 90.05%
OATP1B3 inhibitior + 0.9200 92.00%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9364 93.64%
P-glycoprotein inhibitior - 0.9158 91.58%
P-glycoprotein substrate - 0.8235 82.35%
CYP3A4 substrate + 0.5382 53.82%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.7625 76.25%
CYP3A4 inhibition - 0.8912 89.12%
CYP2C9 inhibition - 0.6735 67.35%
CYP2C19 inhibition - 0.6437 64.37%
CYP2D6 inhibition - 0.9310 93.10%
CYP1A2 inhibition - 0.7737 77.37%
CYP2C8 inhibition - 0.8198 81.98%
CYP inhibitory promiscuity - 0.7224 72.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Warning 0.4772 47.72%
Eye corrosion - 0.9130 91.30%
Eye irritation + 0.9418 94.18%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9800 98.00%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6485 64.85%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5914 59.14%
skin sensitisation + 0.8390 83.90%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5194 51.94%
Acute Oral Toxicity (c) III 0.7890 78.90%
Estrogen receptor binding - 0.8742 87.42%
Androgen receptor binding - 0.6434 64.34%
Thyroid receptor binding - 0.7680 76.80%
Glucocorticoid receptor binding - 0.8077 80.77%
Aromatase binding - 0.7906 79.06%
PPAR gamma - 0.8115 81.15%
Honey bee toxicity - 0.9337 93.37%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5300 53.00%
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 96.97% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.23% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 90.69% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.99% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.53% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.48% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.67% 92.94%
CHEMBL2581 P07339 Cathepsin D 82.82% 98.95%
CHEMBL1871 P10275 Androgen Receptor 82.26% 96.43%

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.
Conocephalum conicum

Cross-Links

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PubChem 73196217
LOTUS LTS0181122
wikiData Q105146062