Phomopsin C

Details

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Internal ID 5c32cf89-617f-409a-85c5-3d549de9a385
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name ethyl 2-(3-hydroxy-5-methoxy-2-octanoylphenyl)acetate
SMILES (Canonical) CCCCCCCC(=O)C1=C(C=C(C=C1O)OC)CC(=O)OCC
SMILES (Isomeric) CCCCCCCC(=O)C1=C(C=C(C=C1O)OC)CC(=O)OCC
InChI InChI=1S/C19H28O5/c1-4-6-7-8-9-10-16(20)19-14(12-18(22)24-5-2)11-15(23-3)13-17(19)21/h11,13,21H,4-10,12H2,1-3H3
InChI Key FXFDGQFKQWWWJW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O5
Molecular Weight 336.40 g/mol
Exact Mass 336.19367399 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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CHEMBL3218046

2D Structure

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2D Structure of Phomopsin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9839 98.39%
Caco-2 + 0.8026 80.26%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.9397 93.97%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.8757 87.57%
OATP1B3 inhibitior + 0.9142 91.42%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8440 84.40%
P-glycoprotein inhibitior - 0.6898 68.98%
P-glycoprotein substrate - 0.8574 85.74%
CYP3A4 substrate + 0.5139 51.39%
CYP2C9 substrate - 0.5995 59.95%
CYP2D6 substrate - 0.8440 84.40%
CYP3A4 inhibition + 0.5148 51.48%
CYP2C9 inhibition - 0.7563 75.63%
CYP2C19 inhibition + 0.5712 57.12%
CYP2D6 inhibition - 0.8736 87.36%
CYP1A2 inhibition + 0.6304 63.04%
CYP2C8 inhibition + 0.6076 60.76%
CYP inhibitory promiscuity - 0.8608 86.08%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7143 71.43%
Carcinogenicity (trinary) Non-required 0.6803 68.03%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.5208 52.08%
Skin irritation - 0.8787 87.87%
Skin corrosion - 0.9785 97.85%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3743 37.43%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5399 53.99%
skin sensitisation - 0.8089 80.89%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.6945 69.45%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5154 51.54%
Acute Oral Toxicity (c) III 0.4592 45.92%
Estrogen receptor binding + 0.6870 68.70%
Androgen receptor binding + 0.5503 55.03%
Thyroid receptor binding - 0.5710 57.10%
Glucocorticoid receptor binding + 0.6940 69.40%
Aromatase binding + 0.6238 62.38%
PPAR gamma + 0.7756 77.56%
Honey bee toxicity - 0.9485 94.85%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7844 78.44%
Fish aquatic toxicity + 0.9945 99.45%

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
CHEMBL230 P35354 Cyclooxygenase-2 97.91% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.79% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.38% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.85% 92.08%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.10% 95.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.06% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.94% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.85% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.10% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.62% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.39% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.29% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.17% 96.95%
CHEMBL4208 P20618 Proteasome component C5 82.10% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.81% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.13% 92.62%

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 24866623
LOTUS LTS0148814
wikiData Q75053134