(4S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-methylcyclohex-2-en-1-one

Details

Top
Internal ID da16e429-56ac-483d-a441-fb5320f1061d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (4S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-methylcyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O3/c1-6-4-9(12)7(5-8(6)11)10(2,3)13/h5-6,8,11,13H,4H2,1-3H3/t6?,8-/m1/s1
InChI Key GTUFHYHOPUHIKF-QFSRMBNQSA-N
Popularity 2 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 0.50
Atomic LogP (AlogP) 0.65
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-methylcyclohex-2-en-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.5433 54.33%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8398 83.98%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.9479 94.79%
OATP1B3 inhibitior + 0.9661 96.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9437 94.37%
P-glycoprotein inhibitior - 0.9654 96.54%
P-glycoprotein substrate - 0.9339 93.39%
CYP3A4 substrate - 0.5700 57.00%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8734 87.34%
CYP3A4 inhibition - 0.8131 81.31%
CYP2C9 inhibition - 0.7048 70.48%
CYP2C19 inhibition - 0.6622 66.22%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.8559 85.59%
CYP2C8 inhibition - 0.9743 97.43%
CYP inhibitory promiscuity - 0.7518 75.18%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7963 79.63%
Carcinogenicity (trinary) Warning 0.4698 46.98%
Eye corrosion - 0.9562 95.62%
Eye irritation + 0.5790 57.90%
Skin irritation - 0.5167 51.67%
Skin corrosion - 0.9206 92.06%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7489 74.89%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.7504 75.04%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5839 58.39%
Acute Oral Toxicity (c) III 0.6262 62.62%
Estrogen receptor binding - 0.9568 95.68%
Androgen receptor binding - 0.9207 92.07%
Thyroid receptor binding - 0.7147 71.47%
Glucocorticoid receptor binding - 0.8920 89.20%
Aromatase binding - 0.9036 90.36%
PPAR gamma - 0.9108 91.08%
Honey bee toxicity - 0.8636 86.36%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9198 91.98%

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
CHEMBL2581 P07339 Cathepsin D 94.26% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.45% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.41% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.91% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.24% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 84.06% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.34% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.19% 97.14%

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.
Nepeta tenuifolia

Cross-Links

Top
PubChem 5321182
NPASS NPC936
LOTUS LTS0230732
wikiData Q105107386