(+)-(4S,5S)-4-hydroxy-3-methoxy-5-methyl-2-cyclopentenone

Details

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Internal ID adf01802-5c2a-4b76-b37b-fae5ad8f2008
Taxonomy Organic acids and derivatives > Vinylogous esters
IUPAC Name (4S,5S)-4-hydroxy-3-methoxy-5-methylcyclopent-2-en-1-one
SMILES (Canonical) CC1C(C(=CC1=O)OC)O
SMILES (Isomeric) C[C@H]1[C@@H](C(=CC1=O)OC)O
InChI InChI=1S/C7H10O3/c1-4-5(8)3-6(10-2)7(4)9/h3-4,7,9H,1-2H3/t4-,7+/m1/s1
InChI Key YEDDGPMINIIFDA-FBCQKBJTSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H10O3
Molecular Weight 142.15 g/mol
Exact Mass 142.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.10
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-(4S,5S)-4-hydroxy-3-methoxy-5-methyl-2-cyclopentenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 - 0.5630 56.30%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8129 81.29%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9419 94.19%
OATP1B3 inhibitior + 0.9765 97.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9512 95.12%
P-glycoprotein inhibitior - 0.9646 96.46%
P-glycoprotein substrate - 0.9573 95.73%
CYP3A4 substrate - 0.6385 63.85%
CYP2C9 substrate - 0.7872 78.72%
CYP2D6 substrate - 0.8621 86.21%
CYP3A4 inhibition - 0.9413 94.13%
CYP2C9 inhibition - 0.9735 97.35%
CYP2C19 inhibition - 0.8184 81.84%
CYP2D6 inhibition - 0.9407 94.07%
CYP1A2 inhibition - 0.7959 79.59%
CYP2C8 inhibition - 0.9881 98.81%
CYP inhibitory promiscuity - 0.8349 83.49%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7850 78.50%
Carcinogenicity (trinary) Non-required 0.5840 58.40%
Eye corrosion + 0.5427 54.27%
Eye irritation + 0.9256 92.56%
Skin irritation + 0.6180 61.80%
Skin corrosion - 0.9035 90.35%
Ames mutagenesis - 0.8054 80.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7913 79.13%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.6658 66.58%
skin sensitisation + 0.4889 48.89%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.4796 47.96%
Acute Oral Toxicity (c) III 0.5151 51.51%
Estrogen receptor binding - 0.8743 87.43%
Androgen receptor binding - 0.7573 75.73%
Thyroid receptor binding - 0.8229 82.29%
Glucocorticoid receptor binding - 0.8696 86.96%
Aromatase binding - 0.8916 89.16%
PPAR gamma - 0.8140 81.40%
Honey bee toxicity - 0.8541 85.41%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.4774 47.74%

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
CHEMBL2581 P07339 Cathepsin D 93.93% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.11% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.76% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.63% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.55% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.73% 86.33%

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 146682633
LOTUS LTS0144091
wikiData Q105347173