4beta,5alpha-Dihydroxy-2,5beta-dimethylcyclohex-2-enone

Details

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Internal ID 6d9dcc9f-ae5e-4b8a-ad7f-a58b089e4f4d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name (4S,5S)-4,5-dihydroxy-2,5-dimethylcyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H12O3/c1-5-3-7(10)8(2,11)4-6(5)9/h3,7,10-11H,4H2,1-2H3/t7-,8-/m0/s1
InChI Key XNSWLALPMYBULY-YUMQZZPRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O3
Molecular Weight 156.18 g/mol
Exact Mass 156.078644241 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP -0.60
Atomic LogP (AlogP) 0.02
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4beta,5alpha-Dihydroxy-2,5beta-dimethylcyclohex-2-enone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.7125 71.25%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7949 79.49%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9460 94.60%
OATP1B3 inhibitior + 0.9750 97.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9112 91.12%
P-glycoprotein inhibitior - 0.9746 97.46%
P-glycoprotein substrate - 0.9489 94.89%
CYP3A4 substrate - 0.5244 52.44%
CYP2C9 substrate - 0.7786 77.86%
CYP2D6 substrate - 0.8630 86.30%
CYP3A4 inhibition - 0.9028 90.28%
CYP2C9 inhibition - 0.8787 87.87%
CYP2C19 inhibition - 0.8597 85.97%
CYP2D6 inhibition - 0.9148 91.48%
CYP1A2 inhibition - 0.8859 88.59%
CYP2C8 inhibition - 0.9847 98.47%
CYP inhibitory promiscuity - 0.9535 95.35%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5138 51.38%
Eye corrosion - 0.9617 96.17%
Eye irritation + 0.8055 80.55%
Skin irritation + 0.5317 53.17%
Skin corrosion - 0.8389 83.89%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8006 80.06%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5868 58.68%
skin sensitisation + 0.6897 68.97%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5528 55.28%
Acute Oral Toxicity (c) III 0.5560 55.60%
Estrogen receptor binding - 0.9463 94.63%
Androgen receptor binding - 0.8166 81.66%
Thyroid receptor binding - 0.8967 89.67%
Glucocorticoid receptor binding - 0.8832 88.32%
Aromatase binding - 0.9304 93.04%
PPAR gamma - 0.8616 86.16%
Honey bee toxicity - 0.9383 93.83%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8804 88.04%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.46% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.09% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.03% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.73% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 81.82% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.64% 97.09%
CHEMBL4208 P20618 Proteasome component C5 80.39% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.17% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139586018
LOTUS LTS0150122
wikiData Q77497055