E,E incanic acid

Details

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Internal ID dac157a2-1e7d-4d5c-868c-c158e454ec5f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E,6E)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-enyl)hept-2-enedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26O5/c1-15(2)6-3-8-17(19(21)22)10-5-11-18(20(23)24)9-4-7-16-12-13-25-14-16/h6,9-10,12-14H,3-5,7-8,11H2,1-2H3,(H,21,22)(H,23,24)/b17-10+,18-9+
InChI Key QZDPUYWKZQBXTJ-SCNFBCNRSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O5
Molecular Weight 346.40 g/mol
Exact Mass 346.17802393 g/mol
Topological Polar Surface Area (TPSA) 87.70 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.76
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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CHEMBL256290
6,10-(E,E)-Thymifodioic Acid
NSC689439
NSC-689439

2D Structure

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2D Structure of E,E incanic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9566 95.66%
Caco-2 - 0.7705 77.05%
Blood Brain Barrier + 0.5605 56.05%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7902 79.02%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.7437 74.37%
OATP1B3 inhibitior + 0.9159 91.59%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7070 70.70%
BSEP inhibitior + 0.8797 87.97%
P-glycoprotein inhibitior - 0.6387 63.87%
P-glycoprotein substrate - 0.9171 91.71%
CYP3A4 substrate - 0.5540 55.40%
CYP2C9 substrate - 0.7818 78.18%
CYP2D6 substrate - 0.9097 90.97%
CYP3A4 inhibition - 0.8074 80.74%
CYP2C9 inhibition - 0.6968 69.68%
CYP2C19 inhibition - 0.7964 79.64%
CYP2D6 inhibition - 0.8813 88.13%
CYP1A2 inhibition - 0.6500 65.00%
CYP2C8 inhibition - 0.8124 81.24%
CYP inhibitory promiscuity - 0.8264 82.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7628 76.28%
Carcinogenicity (trinary) Non-required 0.6459 64.59%
Eye corrosion - 0.9336 93.36%
Eye irritation - 0.7114 71.14%
Skin irritation - 0.7311 73.11%
Skin corrosion - 0.9576 95.76%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4792 47.92%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6552 65.52%
skin sensitisation - 0.6198 61.98%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5339 53.39%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6239 62.39%
Acute Oral Toxicity (c) III 0.6679 66.79%
Estrogen receptor binding + 0.6812 68.12%
Androgen receptor binding - 0.5913 59.13%
Thyroid receptor binding - 0.4946 49.46%
Glucocorticoid receptor binding + 0.5372 53.72%
Aromatase binding + 0.5658 56.58%
PPAR gamma + 0.8641 86.41%
Honey bee toxicity - 0.9405 94.05%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9972 99.72%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.48% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.32% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 90.85% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.68% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.86% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.25% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 84.49% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.95% 96.09%

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.
Baccharis thesioides
Baccharis thymifolia

Cross-Links

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PubChem 5469523
LOTUS LTS0163427
wikiData Q105231878