(4S,8S)-8,9-Dihydroxy-p-mentha-1(6)-ene-2-one

Details

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Internal ID f8246017-b175-4717-9a9a-b3ef129f2d5c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohex-2-en-1-one
SMILES (Canonical) CC1=CCC(CC1=O)C(C)(CO)O
SMILES (Isomeric) CC1=CC[C@@H](CC1=O)[C@@](C)(CO)O
InChI InChI=1S/C10H16O3/c1-7-3-4-8(5-9(7)12)10(2,13)6-11/h3,8,11,13H,4-6H2,1-2H3/t8-,10+/m0/s1
InChI Key AOKPDATZUBLDMG-WCBMZHEXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O3
Molecular Weight 184.23 g/mol
Exact Mass 184.109944368 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.66
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S,8S)-8,9-Dihydroxy-p-mentha-1(6)-ene-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 + 0.9862 98.62%
Caco-2 + 0.6687 66.87%
Blood Brain Barrier - 0.5365 53.65%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8946 89.46%
OATP2B1 inhibitior - 0.8455 84.55%
OATP1B1 inhibitior + 0.9201 92.01%
OATP1B3 inhibitior + 0.9635 96.35%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8679 86.79%
P-glycoprotein inhibitior - 0.9845 98.45%
P-glycoprotein substrate - 0.9109 91.09%
CYP3A4 substrate - 0.5591 55.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8863 88.63%
CYP3A4 inhibition - 0.8571 85.71%
CYP2C9 inhibition - 0.8368 83.68%
CYP2C19 inhibition - 0.8367 83.67%
CYP2D6 inhibition - 0.8819 88.19%
CYP1A2 inhibition - 0.8628 86.28%
CYP2C8 inhibition - 0.9470 94.70%
CYP inhibitory promiscuity - 0.9476 94.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6642 66.42%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.5997 59.97%
Skin irritation - 0.7586 75.86%
Skin corrosion - 0.9588 95.88%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6675 66.75%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5926 59.26%
skin sensitisation - 0.6116 61.16%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5097 50.97%
Acute Oral Toxicity (c) III 0.6523 65.23%
Estrogen receptor binding - 0.9045 90.45%
Androgen receptor binding - 0.7530 75.30%
Thyroid receptor binding - 0.8222 82.22%
Glucocorticoid receptor binding - 0.8259 82.59%
Aromatase binding - 0.8060 80.60%
PPAR gamma - 0.8449 84.49%
Honey bee toxicity - 0.9425 94.25%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9521 95.21%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.19% 97.25%
CHEMBL2581 P07339 Cathepsin D 95.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.89% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.84% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.73% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.28% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 85.20% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 82.15% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.20% 85.14%

Cross-Links

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PubChem 10877793
NPASS NPC179987