10-Hydroxydecanoic Acid

Details

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Internal ID a1a6c2b8-422d-4845-a013-87dacde7646d
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 10-hydroxydecanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H20O3/c11-9-7-5-3-1-2-4-6-8-10(12)13/h11H,1-9H2,(H,12,13)
InChI Key YJCJVMMDTBEITC-UHFFFAOYSA-N
Popularity 183 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O3
Molecular Weight 188.26 g/mol
Exact Mass 188.14124450 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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1679-53-4
10-Hydroxydecanoate
10-hydroxycapric acid
Decanoic acid, 10-hydroxy-
10-HydroxydecanoicAcid
NSC 15139
10-hydroxy capric acid
10-hydroxy-decanoic acid
MFCD00010510
NP03XO416B
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 10-Hydroxydecanoic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9461 94.61%
Caco-2 + 0.4921 49.21%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8504 85.04%
OATP2B1 inhibitior - 0.8488 84.88%
OATP1B1 inhibitior + 0.9444 94.44%
OATP1B3 inhibitior + 0.9443 94.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8188 81.88%
P-glycoprotein inhibitior - 0.9713 97.13%
P-glycoprotein substrate - 0.9880 98.80%
CYP3A4 substrate - 0.7575 75.75%
CYP2C9 substrate - 0.5816 58.16%
CYP2D6 substrate - 0.8592 85.92%
CYP3A4 inhibition - 0.9543 95.43%
CYP2C9 inhibition - 0.9043 90.43%
CYP2C19 inhibition - 0.9622 96.22%
CYP2D6 inhibition - 0.9707 97.07%
CYP1A2 inhibition - 0.9088 90.88%
CYP2C8 inhibition - 0.9814 98.14%
CYP inhibitory promiscuity - 0.9759 97.59%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.7159 71.59%
Eye corrosion + 0.7655 76.55%
Eye irritation + 0.9888 98.88%
Skin irritation - 0.7750 77.50%
Skin corrosion - 0.8965 89.65%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5566 55.66%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6708 67.08%
skin sensitisation - 0.9435 94.35%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.9320 93.20%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5639 56.39%
Acute Oral Toxicity (c) III 0.5988 59.88%
Estrogen receptor binding - 0.8691 86.91%
Androgen receptor binding - 0.8873 88.73%
Thyroid receptor binding - 0.8375 83.75%
Glucocorticoid receptor binding - 0.7855 78.55%
Aromatase binding - 0.7498 74.98%
PPAR gamma - 0.4849 48.49%
Honey bee toxicity - 0.9845 98.45%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8313 83.13%
Fish aquatic toxicity - 0.6286 62.86%

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 92.95% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.46% 99.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 87.08% 92.26%
CHEMBL4040 P28482 MAP kinase ERK2 85.81% 83.82%
CHEMBL1781 P11387 DNA topoisomerase I 83.61% 97.00%
CHEMBL2581 P07339 Cathepsin D 83.26% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.22% 91.11%

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 74300
LOTUS LTS0190389
wikiData Q18343392