5-Hydroxy-3,7,7-trimethylbicyclo[4.1.0]hept-3-en-2-one

Details

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Internal ID 97b15454-47c8-46c2-90fa-87d00cee04bf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 5-hydroxy-3,7,7-trimethylbicyclo[4.1.0]hept-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O2/c1-5-4-6(11)7-8(9(5)12)10(7,2)3/h4,6-8,11H,1-3H3
InChI Key GVTFSJLFFJEHAD-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.15
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-3,7,7-trimethylbicyclo[4.1.0]hept-3-en-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.5342 53.42%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6929 69.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9119 91.19%
OATP1B3 inhibitior + 0.9659 96.59%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9568 95.68%
P-glycoprotein inhibitior - 0.9418 94.18%
P-glycoprotein substrate - 0.9734 97.34%
CYP3A4 substrate - 0.5391 53.91%
CYP2C9 substrate - 0.6830 68.30%
CYP2D6 substrate - 0.8758 87.58%
CYP3A4 inhibition - 0.7838 78.38%
CYP2C9 inhibition - 0.8934 89.34%
CYP2C19 inhibition - 0.6910 69.10%
CYP2D6 inhibition - 0.9111 91.11%
CYP1A2 inhibition - 0.7590 75.90%
CYP2C8 inhibition - 0.9801 98.01%
CYP inhibitory promiscuity - 0.7990 79.90%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7330 73.30%
Carcinogenicity (trinary) Non-required 0.5973 59.73%
Eye corrosion - 0.8608 86.08%
Eye irritation + 0.9298 92.98%
Skin irritation + 0.7007 70.07%
Skin corrosion - 0.8526 85.26%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6691 66.91%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6585 65.85%
skin sensitisation + 0.8093 80.93%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.7337 73.37%
Acute Oral Toxicity (c) III 0.6791 67.91%
Estrogen receptor binding - 0.8624 86.24%
Androgen receptor binding - 0.6950 69.50%
Thyroid receptor binding - 0.8379 83.79%
Glucocorticoid receptor binding - 0.8898 88.98%
Aromatase binding - 0.8641 86.41%
PPAR gamma - 0.8485 84.85%
Honey bee toxicity - 0.8967 89.67%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8818 88.18%

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
CHEMBL2581 P07339 Cathepsin D 90.63% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 89.47% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.99% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.33% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.13% 91.11%

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.
Asarum heterotropoides

Cross-Links

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PubChem 14705611
LOTUS LTS0179489
wikiData Q105021653