6-Hydroxy-3,7-dimethyloctanoic acid

Details

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Internal ID 7e23d29c-0ac7-4e61-8702-4d7cd1ac6d66
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 6-hydroxy-3,7-dimethyloctanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H20O3/c1-7(2)9(11)5-4-8(3)6-10(12)13/h7-9,11H,4-6H2,1-3H3,(H,12,13)
InChI Key IQBGVZDRJBTLDN-UHFFFAOYSA-N
Popularity 3 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 1.90
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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57429-74-0
CHEBI:50451
DTXSID10633868
RefChem:104716
DTXCID70584620
SCHEMBL3893347
LMFA01050370
C18067
Q27122074

2D Structure

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2D Structure of 6-Hydroxy-3,7-dimethyloctanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9723 97.23%
Caco-2 + 0.6806 68.06%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8017 80.17%
OATP2B1 inhibitior - 0.8403 84.03%
OATP1B1 inhibitior + 0.9572 95.72%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9451 94.51%
P-glycoprotein inhibitior - 0.9667 96.67%
P-glycoprotein substrate - 0.9508 95.08%
CYP3A4 substrate - 0.7005 70.05%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate - 0.8625 86.25%
CYP3A4 inhibition - 0.9248 92.48%
CYP2C9 inhibition - 0.8704 87.04%
CYP2C19 inhibition - 0.9396 93.96%
CYP2D6 inhibition - 0.9597 95.97%
CYP1A2 inhibition - 0.6955 69.55%
CYP2C8 inhibition - 0.9964 99.64%
CYP inhibitory promiscuity - 0.9417 94.17%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6815 68.15%
Carcinogenicity (trinary) Non-required 0.7468 74.68%
Eye corrosion + 0.6696 66.96%
Eye irritation + 0.7613 76.13%
Skin irritation - 0.6397 63.97%
Skin corrosion - 0.8862 88.62%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6692 66.92%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5087 50.87%
skin sensitisation + 0.6208 62.08%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6496 64.96%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6302 63.02%
Acute Oral Toxicity (c) III 0.8340 83.40%
Estrogen receptor binding - 0.9277 92.77%
Androgen receptor binding - 0.8514 85.14%
Thyroid receptor binding - 0.7414 74.14%
Glucocorticoid receptor binding - 0.8082 80.82%
Aromatase binding - 0.8388 83.88%
PPAR gamma - 0.9345 93.45%
Honey bee toxicity - 0.9622 96.22%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity + 0.7917 79.17%

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 95.38% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.57% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.70% 85.14%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.39% 96.47%
CHEMBL221 P23219 Cyclooxygenase-1 86.35% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 85.87% 83.82%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.43% 100.00%
CHEMBL3776 Q14790 Caspase-8 83.58% 97.06%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.60% 99.17%

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 23422948
LOTUS LTS0200688
wikiData Q27122074