Phlebiachrysoic acid E

Details

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Internal ID 53af9369-f964-4e0b-a5db-7e0a098e815e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (E)-17-(2-hydroxy-5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)heptadec-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H36O6/c1-30-21-18-20(25)23(28)19(24(21)29)16-14-12-10-8-6-4-2-3-5-7-9-11-13-15-17-22(26)27/h15,17-18,28H,2-14,16H2,1H3,(H,26,27)/b17-15+
InChI Key DCIFWGHOSANJTJ-BMRADRMJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H36O6
Molecular Weight 420.50 g/mol
Exact Mass 420.25118886 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 7.10
Atomic LogP (AlogP) 5.58
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phlebiachrysoic acid E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8808 88.08%
Caco-2 - 0.7102 71.02%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.9254 92.54%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.8982 89.82%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5533 55.33%
P-glycoprotein inhibitior + 0.5999 59.99%
P-glycoprotein substrate - 0.8075 80.75%
CYP3A4 substrate + 0.5182 51.82%
CYP2C9 substrate - 0.7808 78.08%
CYP2D6 substrate - 0.8826 88.26%
CYP3A4 inhibition - 0.9621 96.21%
CYP2C9 inhibition - 0.8019 80.19%
CYP2C19 inhibition - 0.8054 80.54%
CYP2D6 inhibition - 0.8293 82.93%
CYP1A2 inhibition - 0.8466 84.66%
CYP2C8 inhibition - 0.6254 62.54%
CYP inhibitory promiscuity - 0.9259 92.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8272 82.72%
Carcinogenicity (trinary) Non-required 0.6841 68.41%
Eye corrosion - 0.9513 95.13%
Eye irritation - 0.5848 58.48%
Skin irritation - 0.7270 72.70%
Skin corrosion - 0.9697 96.97%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3753 37.53%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5073 50.73%
skin sensitisation - 0.7959 79.59%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5666 56.66%
Acute Oral Toxicity (c) III 0.4967 49.67%
Estrogen receptor binding + 0.6571 65.71%
Androgen receptor binding + 0.7546 75.46%
Thyroid receptor binding - 0.5261 52.61%
Glucocorticoid receptor binding + 0.5501 55.01%
Aromatase binding - 0.5258 52.58%
PPAR gamma + 0.6805 68.05%
Honey bee toxicity - 0.9357 93.57%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5324 53.24%
Fish aquatic toxicity + 0.9594 95.94%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.48% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.42% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.55% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.93% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.29% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.47% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.58% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.97% 94.33%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.90% 92.68%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.62% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.40% 94.45%

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 21635348
LOTUS LTS0259855
wikiData Q77501439