2-(8-Hydroxyoctylidene)-3-methylidenebutanedioic acid

Details

Top
Internal ID 63582987-1e47-431c-b800-619e78e875fd
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 2-(8-hydroxyoctylidene)-3-methylidenebutanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H20O5/c1-10(12(15)16)11(13(17)18)8-6-4-2-3-5-7-9-14/h8,14H,1-7,9H2,(H,15,16)(H,17,18)
InChI Key CDMKEGLENKKMCC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H20O5
Molecular Weight 256.29 g/mol
Exact Mass 256.13107373 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(8-Hydroxyoctylidene)-3-methylidenebutanedioic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8154 81.54%
Caco-2 - 0.7235 72.35%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8338 83.38%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9167 91.67%
OATP1B3 inhibitior + 0.9484 94.84%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9458 94.58%
P-glycoprotein inhibitior - 0.9367 93.67%
P-glycoprotein substrate - 0.9449 94.49%
CYP3A4 substrate - 0.6148 61.48%
CYP2C9 substrate - 0.7683 76.83%
CYP2D6 substrate - 0.8941 89.41%
CYP3A4 inhibition - 0.8005 80.05%
CYP2C9 inhibition - 0.8739 87.39%
CYP2C19 inhibition - 0.9202 92.02%
CYP2D6 inhibition - 0.9220 92.20%
CYP1A2 inhibition - 0.8924 89.24%
CYP2C8 inhibition - 0.9232 92.32%
CYP inhibitory promiscuity - 0.9685 96.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.7655 76.55%
Eye corrosion - 0.6499 64.99%
Eye irritation + 0.9372 93.72%
Skin irritation - 0.7508 75.08%
Skin corrosion - 0.9748 97.48%
Ames mutagenesis - 0.8254 82.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5877 58.77%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6697 66.97%
skin sensitisation - 0.7560 75.60%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5289 52.89%
Acute Oral Toxicity (c) III 0.6759 67.59%
Estrogen receptor binding + 0.5556 55.56%
Androgen receptor binding - 0.6636 66.36%
Thyroid receptor binding - 0.6653 66.53%
Glucocorticoid receptor binding + 0.6616 66.16%
Aromatase binding - 0.5403 54.03%
PPAR gamma + 0.8375 83.75%
Honey bee toxicity - 0.9406 94.06%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6959 69.59%
Fish aquatic toxicity + 0.9166 91.66%

Targets

Top

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
CHEMBL3060 Q9Y345 Glycine transporter 2 91.50% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.30% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.04% 96.95%
CHEMBL1829 O15379 Histone deacetylase 3 81.95% 95.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.91% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.68% 97.29%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.26% 94.45%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 24013836
LOTUS LTS0267715
wikiData Q103817632