(2E,6E,10Z)-12-hydroxy-10-(hydroxymethyl)-6-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienoic acid

Details

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Internal ID 51bbc582-2764-404f-a894-f6b18ad02f2c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (2E,6E,10Z)-12-hydroxy-10-(hydroxymethyl)-6-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O4/c1-16(2)7-4-11-19(20(23)24)12-6-9-17(3)8-5-10-18(15-22)13-14-21/h7-8,12-13,21-22H,4-6,9-11,14-15H2,1-3H3,(H,23,24)/b17-8+,18-13-,19-12+
InChI Key GWVCYAYKRPLWGK-AAMZJHKISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O4
Molecular Weight 336.50 g/mol
Exact Mass 336.23005950 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.16
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 12

Synonyms

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MEGxp0_000999
ACon0_000337
ACon1_000945
DTXSID60904191
NCGC00169204-01

2D Structure

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2D Structure of (2E,6E,10Z)-12-hydroxy-10-(hydroxymethyl)-6-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9381 93.81%
Caco-2 + 0.5137 51.37%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6754 67.54%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9095 90.95%
OATP1B3 inhibitior + 0.9030 90.30%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8468 84.68%
P-glycoprotein inhibitior - 0.7105 71.05%
P-glycoprotein substrate - 0.8944 89.44%
CYP3A4 substrate - 0.5151 51.51%
CYP2C9 substrate - 0.5754 57.54%
CYP2D6 substrate - 0.9111 91.11%
CYP3A4 inhibition - 0.8507 85.07%
CYP2C9 inhibition - 0.8301 83.01%
CYP2C19 inhibition - 0.8957 89.57%
CYP2D6 inhibition - 0.8994 89.94%
CYP1A2 inhibition - 0.8565 85.65%
CYP2C8 inhibition - 0.9354 93.54%
CYP inhibitory promiscuity - 0.8907 89.07%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7223 72.23%
Carcinogenicity (trinary) Non-required 0.6959 69.59%
Eye corrosion - 0.8706 87.06%
Eye irritation + 0.6399 63.99%
Skin irritation - 0.7376 73.76%
Skin corrosion - 0.9850 98.50%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6166 61.66%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation - 0.5830 58.30%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.8976 89.76%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5906 59.06%
Acute Oral Toxicity (c) IV 0.7180 71.80%
Estrogen receptor binding + 0.6210 62.10%
Androgen receptor binding - 0.6637 66.37%
Thyroid receptor binding + 0.6694 66.94%
Glucocorticoid receptor binding + 0.5515 55.15%
Aromatase binding + 0.6622 66.22%
PPAR gamma + 0.9088 90.88%
Honey bee toxicity - 0.9069 90.69%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9867 98.67%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.60% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.78% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.25% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.75% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.08% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.78% 96.95%

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.
Gutierrezia resinosa

Cross-Links

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PubChem 23872020
LOTUS LTS0143094
wikiData Q82873430