12-Hydroxydodecanoic Acid

Details

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Internal ID 2e518a7e-4f7b-4b3f-bfa9-389615b86072
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 12-hydroxydodecanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H24O3/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15/h13H,1-11H2,(H,14,15)
InChI Key ZDHCZVWCTKTBRY-UHFFFAOYSA-N
Popularity 190 references in papers

Physical and Chemical Properties

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Molecular Formula C12H24O3
Molecular Weight 216.32 g/mol
Exact Mass 216.17254462 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.96
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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505-95-3
12-hydroxylauric acid
Dodecanoic acid, 12-hydroxy-
12-hydroxy-dodecanoic acid
Sabinic acid
Dodecanoic acid,12-hydroxy-
12-hydroxy lauric acid
12-HYDROXYDODECANOICACID
omega-Hydroxydodecanoic acid
CHEBI:39567
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 12-Hydroxydodecanoic 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 - 0.5267 52.67%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8504 85.04%
OATP2B1 inhibitior - 0.8504 85.04%
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 - 0.8287 82.87%
P-glycoprotein inhibitior - 0.9533 95.33%
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 + 0.9801 98.01%
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 - 0.4829 48.29%
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 - 0.8852 88.52%
Androgen receptor binding - 0.8774 87.74%
Thyroid receptor binding - 0.7486 74.86%
Glucocorticoid receptor binding - 0.8082 80.82%
Aromatase binding - 0.7031 70.31%
PPAR gamma + 0.6532 65.32%
Honey bee toxicity - 0.9845 98.45%
Biodegradation + 0.9500 95.00%
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!
To see more specific details click the taxa you are interested in.
Pinus radiata

Cross-Links

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PubChem 79034
LOTUS LTS0039167
wikiData Q27070761