4-Hydroxy-5-(2-hydroxyethyl)-2-(hydroxymethyl)cyclopentene-1-carboxylic acid

Details

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Internal ID be8133bf-7c42-460e-854c-4c2cf88f2310
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Iridoids and derivatives
IUPAC Name 4-hydroxy-5-(2-hydroxyethyl)-2-(hydroxymethyl)cyclopentene-1-carboxylic acid
SMILES (Canonical) C1C(C(C(=C1CO)C(=O)O)CCO)O
SMILES (Isomeric) C1C(C(C(=C1CO)C(=O)O)CCO)O
InChI InChI=1S/C9H14O5/c10-2-1-6-7(12)3-5(4-11)8(6)9(13)14/h6-7,10-12H,1-4H2,(H,13,14)
InChI Key HYJIDONKRRKLEJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O5
Molecular Weight 202.20 g/mol
Exact Mass 202.08412354 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP -1.90
Atomic LogP (AlogP) -0.88
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-5-(2-hydroxyethyl)-2-(hydroxymethyl)cyclopentene-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9291 92.91%
Caco-2 - 0.8988 89.88%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8818 88.18%
OATP2B1 inhibitior - 0.8434 84.34%
OATP1B1 inhibitior + 0.9457 94.57%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6320 63.20%
BSEP inhibitior - 0.9655 96.55%
P-glycoprotein inhibitior - 0.9778 97.78%
P-glycoprotein substrate - 0.9196 91.96%
CYP3A4 substrate - 0.6547 65.47%
CYP2C9 substrate + 0.6018 60.18%
CYP2D6 substrate - 0.8898 88.98%
CYP3A4 inhibition - 0.9699 96.99%
CYP2C9 inhibition - 0.9343 93.43%
CYP2C19 inhibition - 0.8586 85.86%
CYP2D6 inhibition - 0.9000 90.00%
CYP1A2 inhibition - 0.8992 89.92%
CYP2C8 inhibition - 0.9471 94.71%
CYP inhibitory promiscuity - 0.9517 95.17%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9228 92.28%
Carcinogenicity (trinary) Non-required 0.7331 73.31%
Eye corrosion - 0.9633 96.33%
Eye irritation + 0.7885 78.85%
Skin irritation - 0.7732 77.32%
Skin corrosion - 0.9712 97.12%
Ames mutagenesis + 0.5677 56.77%
Human Ether-a-go-go-Related Gene inhibition - 0.6805 68.05%
Micronuclear - 0.8941 89.41%
Hepatotoxicity + 0.5263 52.63%
skin sensitisation - 0.8082 80.82%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5274 52.74%
Acute Oral Toxicity (c) III 0.7600 76.00%
Estrogen receptor binding - 0.8889 88.89%
Androgen receptor binding - 0.7876 78.76%
Thyroid receptor binding - 0.7303 73.03%
Glucocorticoid receptor binding - 0.5160 51.60%
Aromatase binding - 0.8531 85.31%
PPAR gamma - 0.5735 57.35%
Honey bee toxicity - 0.9702 97.02%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.7346 73.46%

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 94.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.63% 91.11%
CHEMBL2581 P07339 Cathepsin D 83.83% 98.95%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.56% 95.71%
CHEMBL1881 P43116 Prostanoid EP2 receptor 81.68% 93.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.01% 96.95%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.89% 93.00%

Plants that contains it

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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.
Crescentia cujete
Vitex trifolia subsp. litoralis

Cross-Links

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PubChem 85255658
LOTUS LTS0143668
wikiData Q105035338