(3aS,4S,7R,7aS)-3a,7a-Dimethyl-3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoindene

Details

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Internal ID 662a4751-71d8-4674-8153-7d8733413209
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids
IUPAC Name 2,6-dimethyltricyclo[5.2.1.02,6]dec-3-ene
SMILES (Canonical) CC12CC=CC1(C3CCC2C3)C
SMILES (Isomeric) CC12CC=CC1(C3CCC2C3)C
InChI InChI=1S/C12H18/c1-11-6-3-7-12(11,2)10-5-4-9(11)8-10/h3,6,9-10H,4-5,7-8H2,1-2H3
InChI Key HKLBEHRJWPWLOB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2,6-dimethyltricyclo[5.2.1.0?,?]dec-3-ene
(3aS,4S,7R,7aS)-3a,7a-Dimethyl-3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoindene
4,7-Methano-1H-indene, 3a,4,5,6,7,7a-hexahydro-3a,7a-dimethyl-, [3aS-(3a.alpha.,4.beta.,7.beta.,7a.alpha.)]-

2D Structure

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2D Structure of (3aS,4S,7R,7aS)-3a,7a-Dimethyl-3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoindene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.9175 91.75%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.8151 81.51%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.9377 93.77%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9141 91.41%
P-glycoprotein inhibitior - 0.9773 97.73%
P-glycoprotein substrate - 0.8783 87.83%
CYP3A4 substrate + 0.5130 51.30%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.7615 76.15%
CYP3A4 inhibition - 0.8919 89.19%
CYP2C9 inhibition - 0.9219 92.19%
CYP2C19 inhibition - 0.8844 88.44%
CYP2D6 inhibition - 0.9595 95.95%
CYP1A2 inhibition - 0.7930 79.30%
CYP2C8 inhibition - 0.8363 83.63%
CYP inhibitory promiscuity - 0.7960 79.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4947 49.47%
Eye corrosion - 0.8031 80.31%
Eye irritation + 0.7965 79.65%
Skin irritation + 0.5143 51.43%
Skin corrosion - 0.9805 98.05%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6515 65.15%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6867 68.67%
skin sensitisation + 0.9059 90.59%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5257 52.57%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.4583 45.83%
Acute Oral Toxicity (c) III 0.5259 52.59%
Estrogen receptor binding - 0.7727 77.27%
Androgen receptor binding - 0.7505 75.05%
Thyroid receptor binding - 0.8123 81.23%
Glucocorticoid receptor binding - 0.8167 81.67%
Aromatase binding - 0.7228 72.28%
PPAR gamma - 0.7989 79.89%
Honey bee toxicity - 0.8400 84.00%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9970 99.70%

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 93.19% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.59% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.34% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.99% 92.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.36% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 83.90% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.86% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.16% 95.89%

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.
Inula helenium
Petasites hybridus

Cross-Links

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PubChem 15558667
NPASS NPC90374
LOTUS LTS0049965
wikiData Q105029727