(E,Z,Z,Z)-2-(9-Hydroxy-4,8-dimethyl-3,7-nonadienyl)-6-methyl-2,6-octadienedioic acid

Details

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Internal ID 61b64f9f-fd8a-46f1-846c-027b0972cbf9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (2E,6Z)-2-[(3Z,7Z)-9-hydroxy-4,8-dimethylnona-3,7-dienyl]-6-methylocta-2,6-dienedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O5/c1-15(7-4-10-17(3)14-21)8-5-11-18(20(24)25)12-6-9-16(2)13-19(22)23/h8,10,12-13,21H,4-7,9,11,14H2,1-3H3,(H,22,23)(H,24,25)/b15-8-,16-13-,17-10-,18-12+
InChI Key FGJWXLZRPBWZLH-NHJMLNGISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O5
Molecular Weight 350.40 g/mol
Exact Mass 350.20932405 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,Z,Z,Z)-2-(9-Hydroxy-4,8-dimethyl-3,7-nonadienyl)-6-methyl-2,6-octadienedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9334 93.34%
Caco-2 + 0.5746 57.46%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7194 71.94%
OATP2B1 inhibitior - 0.7160 71.60%
OATP1B1 inhibitior + 0.9020 90.20%
OATP1B3 inhibitior + 0.9198 91.98%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7102 71.02%
BSEP inhibitior + 0.8343 83.43%
P-glycoprotein inhibitior - 0.7243 72.43%
P-glycoprotein substrate - 0.9108 91.08%
CYP3A4 substrate - 0.5497 54.97%
CYP2C9 substrate - 0.5754 57.54%
CYP2D6 substrate - 0.9111 91.11%
CYP3A4 inhibition - 0.6970 69.70%
CYP2C9 inhibition - 0.7963 79.63%
CYP2C19 inhibition - 0.8936 89.36%
CYP2D6 inhibition - 0.8655 86.55%
CYP1A2 inhibition - 0.7800 78.00%
CYP2C8 inhibition - 0.9272 92.72%
CYP inhibitory promiscuity - 0.9128 91.28%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7323 73.23%
Carcinogenicity (trinary) Non-required 0.7246 72.46%
Eye corrosion - 0.9025 90.25%
Eye irritation - 0.5231 52.31%
Skin irritation - 0.7449 74.49%
Skin corrosion - 0.9880 98.80%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4625 46.25%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.6975 69.75%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8812 88.12%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5679 56.79%
Acute Oral Toxicity (c) IV 0.5001 50.01%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.5374 53.74%
Thyroid receptor binding + 0.5884 58.84%
Glucocorticoid receptor binding - 0.4857 48.57%
Aromatase binding - 0.5629 56.29%
PPAR gamma + 0.8756 87.56%
Honey bee toxicity - 0.9166 91.66%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9915 99.15%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 87.52% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.61% 92.08%
CHEMBL2581 P07339 Cathepsin D 83.33% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.57% 96.09%
CHEMBL2061 P19793 Retinoid X receptor alpha 80.03% 91.67%

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.
Eremophila exilifolia

Cross-Links

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PubChem 163184467
LOTUS LTS0247976
wikiData Q104994928