(2E,4E,6R)-8-hydroxy-6-methylocta-2,4-dienoic acid

Details

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Internal ID 96bfd8c0-caf1-4145-9f73-c0b7edd7937e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name (2E,4E,6R)-8-hydroxy-6-methylocta-2,4-dienoic acid
SMILES (Canonical) CC(CCO)C=CC=CC(=O)O
SMILES (Isomeric) C[C@H](CCO)/C=C/C=C/C(=O)O
InChI InChI=1S/C9H14O3/c1-8(6-7-10)4-2-3-5-9(11)12/h2-5,8,10H,6-7H2,1H3,(H,11,12)/b4-2+,5-3+/t8-/m0/s1
InChI Key KFHQGKGXRZPBOB-HKQWHQQWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O3
Molecular Weight 170.21 g/mol
Exact Mass 170.094294304 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,4E,6R)-8-hydroxy-6-methylocta-2,4-dienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 + 0.9012 90.12%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6299 62.99%
OATP2B1 inhibitior - 0.8653 86.53%
OATP1B1 inhibitior + 0.9194 91.94%
OATP1B3 inhibitior + 0.9317 93.17%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9396 93.96%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9337 93.37%
CYP3A4 substrate - 0.6498 64.98%
CYP2C9 substrate - 0.7818 78.18%
CYP2D6 substrate - 0.9108 91.08%
CYP3A4 inhibition - 0.9398 93.98%
CYP2C9 inhibition - 0.9559 95.59%
CYP2C19 inhibition - 0.9436 94.36%
CYP2D6 inhibition - 0.9536 95.36%
CYP1A2 inhibition - 0.6935 69.35%
CYP2C8 inhibition - 0.9883 98.83%
CYP inhibitory promiscuity - 0.9712 97.12%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7737 77.37%
Eye corrosion + 0.9099 90.99%
Eye irritation - 0.5281 52.81%
Skin irritation + 0.7534 75.34%
Skin corrosion + 0.8394 83.94%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7635 76.35%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6039 60.39%
skin sensitisation - 0.7269 72.69%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7806 78.06%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.5662 56.62%
Acute Oral Toxicity (c) III 0.8494 84.94%
Estrogen receptor binding - 0.9489 94.89%
Androgen receptor binding - 0.8640 86.40%
Thyroid receptor binding - 0.8650 86.50%
Glucocorticoid receptor binding - 0.7011 70.11%
Aromatase binding - 0.7331 73.31%
PPAR gamma - 0.6043 60.43%
Honey bee toxicity - 0.9604 96.04%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.4947 49.47%

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 89.98% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.29% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 84.81% 83.82%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.64% 96.47%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.53% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.15% 93.56%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.14% 98.75%
CHEMBL2581 P07339 Cathepsin D 80.87% 98.95%

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 13963191
LOTUS LTS0034712
wikiData Q105140375