(2S,3R)-2,3-dihydroxy-3-methyl-6-propan-2-ylidenecyclohexan-1-one

Details

Top
Internal ID bd5d206e-2377-473a-b841-763a6226342f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (2S,3R)-2,3-dihydroxy-3-methyl-6-propan-2-ylidenecyclohexan-1-one
SMILES (Canonical) CC(=C1CCC(C(C1=O)O)(C)O)C
SMILES (Isomeric) CC(=C1CC[C@@]([C@@H](C1=O)O)(C)O)C
InChI InChI=1S/C10H16O3/c1-6(2)7-4-5-10(3,13)9(12)8(7)11/h9,12-13H,4-5H2,1-3H3/t9-,10-/m1/s1
InChI Key POWIZHOBIKYRGK-NXEZZACHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H16O3
Molecular Weight 184.23 g/mol
Exact Mass 184.109944368 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.80
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2S,3R)-2,3-dihydroxy-3-methyl-6-propan-2-ylidenecyclohexan-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.5192 51.92%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7830 78.30%
OATP2B1 inhibitior - 0.8412 84.12%
OATP1B1 inhibitior + 0.9578 95.78%
OATP1B3 inhibitior + 0.9593 95.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9021 90.21%
P-glycoprotein inhibitior - 0.9743 97.43%
P-glycoprotein substrate - 0.9601 96.01%
CYP3A4 substrate - 0.5076 50.76%
CYP2C9 substrate - 0.7846 78.46%
CYP2D6 substrate - 0.8659 86.59%
CYP3A4 inhibition - 0.8629 86.29%
CYP2C9 inhibition - 0.7474 74.74%
CYP2C19 inhibition - 0.7652 76.52%
CYP2D6 inhibition - 0.9163 91.63%
CYP1A2 inhibition - 0.8353 83.53%
CYP2C8 inhibition - 0.9863 98.63%
CYP inhibitory promiscuity - 0.9280 92.80%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5335 53.35%
Eye corrosion - 0.9832 98.32%
Eye irritation + 0.9367 93.67%
Skin irritation + 0.6158 61.58%
Skin corrosion - 0.8877 88.77%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6979 69.79%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7396 73.96%
skin sensitisation + 0.6041 60.41%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5596 55.96%
Acute Oral Toxicity (c) III 0.6552 65.52%
Estrogen receptor binding - 0.8823 88.23%
Androgen receptor binding - 0.7102 71.02%
Thyroid receptor binding - 0.7141 71.41%
Glucocorticoid receptor binding - 0.7599 75.99%
Aromatase binding - 0.8830 88.30%
PPAR gamma - 0.7579 75.79%
Honey bee toxicity - 0.9381 93.81%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8874 88.74%

Targets

Top

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 92.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.75% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.89% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.19% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.55% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.15% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.24% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.39% 99.23%

Plants that contains it

Top
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.
Mentha spicata subsp. condensata

Cross-Links

Top
PubChem 130756218
LOTUS LTS0249210
wikiData Q105212718