Carvone-5,6-oxide, cis-(-)-

Details

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Internal ID 965f009a-0a47-4724-899f-156aa30a272f
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (1S,4R,6S)-1-methyl-4-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O2/c1-6(2)7-4-8(11)10(3)9(5-7)12-10/h7,9H,1,4-5H2,2-3H3/t7-,9-,10+/m0/s1
InChI Key YGMNGQDLUQECTO-UJNFCWOMSA-N
Popularity 5 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) 29.60 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.70
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Carvone-5,6-oxide, cis-(-)-
(1S,4R,6S)-1-Methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptan-2-one
Carvone oxide, cis-
(1S,4R,6S)-1-methyl-4-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptan-2-one
TV5341W478
cis-Carvone oxide
UNII-TV5341W478
1,6-Epoxy-p-menth-8-en-2-one, (1S,4R,6S)-
cis-(-)-carvone-5,6-oxide
P-Menth-8-en-2-one, 1,6-epoxy-, (1S,4R6S)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Carvone-5,6-oxide, cis-(-)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 - 0.5140 51.40%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4749 47.49%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9399 93.99%
OATP1B3 inhibitior + 0.9623 96.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8862 88.62%
P-glycoprotein inhibitior - 0.9695 96.95%
P-glycoprotein substrate - 0.9201 92.01%
CYP3A4 substrate + 0.5226 52.26%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7762 77.62%
CYP3A4 inhibition - 0.8653 86.53%
CYP2C9 inhibition - 0.9042 90.42%
CYP2C19 inhibition - 0.6270 62.70%
CYP2D6 inhibition - 0.9407 94.07%
CYP1A2 inhibition - 0.6177 61.77%
CYP2C8 inhibition - 0.9512 95.12%
CYP inhibitory promiscuity - 0.9017 90.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6159 61.59%
Eye corrosion - 0.9428 94.28%
Eye irritation + 0.8301 83.01%
Skin irritation + 0.5348 53.48%
Skin corrosion - 0.9162 91.62%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5567 55.67%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.6852 68.52%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.8836 88.36%
Acute Oral Toxicity (c) III 0.6139 61.39%
Estrogen receptor binding - 0.8824 88.24%
Androgen receptor binding - 0.6645 66.45%
Thyroid receptor binding - 0.8269 82.69%
Glucocorticoid receptor binding - 0.8564 85.64%
Aromatase binding - 0.7798 77.98%
PPAR gamma - 0.8213 82.13%
Honey bee toxicity - 0.7967 79.67%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8936 89.36%

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 97.92% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.07% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.97% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.29% 97.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.10% 85.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.59% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.31% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.23% 95.56%

Cross-Links

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PubChem 11030188
NPASS NPC91931
LOTUS LTS0071453
wikiData Q27290410