(Z)-2-(5-hydroxyhex-yl)pent-2-enedioic acid

Details

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Internal ID fefb2421-61db-4847-848b-15f70f57f648
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name (Z)-2-(5-hydroxyhexyl)pent-2-enedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H18O5/c1-8(12)4-2-3-5-9(11(15)16)6-7-10(13)14/h6,8,12H,2-5,7H2,1H3,(H,13,14)(H,15,16)/b9-6-
InChI Key BNAMTCVIFSTQOZ-TWGQIWQCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O5
Molecular Weight 230.26 g/mol
Exact Mass 230.11542367 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-2-(5-hydroxyhex-yl)pent-2-enedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9264 92.64%
Caco-2 - 0.5872 58.72%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8058 80.58%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9123 91.23%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9657 96.57%
P-glycoprotein inhibitior - 0.9882 98.82%
P-glycoprotein substrate - 0.9226 92.26%
CYP3A4 substrate - 0.5760 57.60%
CYP2C9 substrate - 0.5754 57.54%
CYP2D6 substrate - 0.8995 89.95%
CYP3A4 inhibition - 0.9097 90.97%
CYP2C9 inhibition - 0.9262 92.62%
CYP2C19 inhibition - 0.9453 94.53%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.6615 66.15%
CYP2C8 inhibition - 0.9868 98.68%
CYP inhibitory promiscuity - 0.9527 95.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7735 77.35%
Carcinogenicity (trinary) Non-required 0.7290 72.90%
Eye corrosion - 0.8171 81.71%
Eye irritation + 0.8800 88.00%
Skin irritation - 0.6630 66.30%
Skin corrosion - 0.9583 95.83%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7633 76.33%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5716 57.16%
skin sensitisation - 0.7058 70.58%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.8648 86.48%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7670 76.70%
Acute Oral Toxicity (c) III 0.6504 65.04%
Estrogen receptor binding - 0.6457 64.57%
Androgen receptor binding - 0.7348 73.48%
Thyroid receptor binding - 0.7794 77.94%
Glucocorticoid receptor binding - 0.5632 56.32%
Aromatase binding - 0.7185 71.85%
PPAR gamma + 0.5454 54.54%
Honey bee toxicity - 0.9534 95.34%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.9746 97.46%

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
CHEMBL2581 P07339 Cathepsin D 94.47% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.47% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.49% 99.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 88.57% 96.47%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.13% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.06% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.66% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.23% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.79% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.66% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.90% 90.71%

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 101893002
LOTUS LTS0114524
wikiData Q77372410