4,5-Dihydroxy-3-(1-hydroxyhex-4-enyl)-2,5-dimethylcyclopent-2-en-1-one

Details

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Internal ID 75a9b638-073d-41de-938d-7eeefff570d2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 4,5-dihydroxy-3-(1-hydroxyhex-4-enyl)-2,5-dimethylcyclopent-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H20O4/c1-4-5-6-7-9(14)10-8(2)11(15)13(3,17)12(10)16/h4-5,9,12,14,16-17H,6-7H2,1-3H3
InChI Key MDJUYTDLJQDSHN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O4
Molecular Weight 240.29 g/mol
Exact Mass 240.13615911 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.71
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,5-Dihydroxy-3-(1-hydroxyhex-4-enyl)-2,5-dimethylcyclopent-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9060 90.60%
Caco-2 - 0.6084 60.84%
Blood Brain Barrier + 0.7149 71.49%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6237 62.37%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.8683 86.83%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7076 70.76%
P-glycoprotein inhibitior - 0.9423 94.23%
P-glycoprotein substrate - 0.8662 86.62%
CYP3A4 substrate + 0.5511 55.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8506 85.06%
CYP3A4 inhibition - 0.9284 92.84%
CYP2C9 inhibition - 0.7988 79.88%
CYP2C19 inhibition - 0.7419 74.19%
CYP2D6 inhibition - 0.9148 91.48%
CYP1A2 inhibition - 0.8556 85.56%
CYP2C8 inhibition - 0.9594 95.94%
CYP inhibitory promiscuity - 0.9159 91.59%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6450 64.50%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.9790 97.90%
Skin irritation + 0.5452 54.52%
Skin corrosion - 0.8754 87.54%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6422 64.22%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation - 0.6595 65.95%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7034 70.34%
Acute Oral Toxicity (c) III 0.5556 55.56%
Estrogen receptor binding - 0.6583 65.83%
Androgen receptor binding - 0.7144 71.44%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6470 64.70%
Aromatase binding - 0.7599 75.99%
PPAR gamma - 0.5667 56.67%
Honey bee toxicity - 0.8379 83.79%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.3651 36.51%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.05% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.33% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.65% 98.95%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 88.15% 96.47%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.74% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.74% 85.14%
CHEMBL1907 P15144 Aminopeptidase N 83.72% 93.31%

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 162815378
LOTUS LTS0040187
wikiData Q104171578