Hypocrenone C

Details

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Internal ID fec16626-119a-4325-85e9-43b81c3db792
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (E)-3-(3-oxocyclopenten-1-yl)prop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8O3/c9-7-3-1-6(5-7)2-4-8(10)11/h2,4-5H,1,3H2,(H,10,11)/b4-2+
InChI Key FIXFJSCIIIVDHU-DUXPYHPUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O3
Molecular Weight 152.15 g/mol
Exact Mass 152.047344113 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.92
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hypocrenone C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 + 0.7437 74.37%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.8533 85.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9440 94.40%
OATP1B3 inhibitior + 0.9533 95.33%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9181 91.81%
P-glycoprotein inhibitior - 0.9936 99.36%
P-glycoprotein substrate - 0.9811 98.11%
CYP3A4 substrate - 0.6935 69.35%
CYP2C9 substrate - 0.7709 77.09%
CYP2D6 substrate - 0.8838 88.38%
CYP3A4 inhibition - 0.9410 94.10%
CYP2C9 inhibition - 0.9421 94.21%
CYP2C19 inhibition - 0.9315 93.15%
CYP2D6 inhibition - 0.9137 91.37%
CYP1A2 inhibition - 0.9079 90.79%
CYP2C8 inhibition - 0.9425 94.25%
CYP inhibitory promiscuity - 0.9771 97.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8024 80.24%
Carcinogenicity (trinary) Non-required 0.6218 62.18%
Eye corrosion + 0.6445 64.45%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.6623 66.23%
Skin corrosion - 0.7649 76.49%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8114 81.14%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5741 57.41%
skin sensitisation + 0.5542 55.42%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.4536 45.36%
Acute Oral Toxicity (c) III 0.4765 47.65%
Estrogen receptor binding - 0.9606 96.06%
Androgen receptor binding - 0.5849 58.49%
Thyroid receptor binding - 0.8349 83.49%
Glucocorticoid receptor binding - 0.7952 79.52%
Aromatase binding - 0.8347 83.47%
PPAR gamma - 0.6524 65.24%
Honey bee toxicity - 0.9560 95.60%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.95% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.15% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.48% 86.33%
CHEMBL4040 P28482 MAP kinase ERK2 80.21% 83.82%

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 139588008
LOTUS LTS0268373
wikiData Q104995917