Chrysine A

Details

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Internal ID faa2d634-bcfe-4155-a120-7633d18af2de
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 2-(2,4-dichloro-5-hydroxy-6-methoxycarbonyl-3-methylphenoxy)-3,5-dimethoxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16Cl2O8/c1-7-12(19)14(21)11(18(24)27-4)16(13(7)20)28-15-9(17(22)23)5-8(25-2)6-10(15)26-3/h5-6,21H,1-4H3,(H,22,23)
InChI Key MLUAYUWFBGUTHY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16Cl2O8
Molecular Weight 431.20 g/mol
Exact Mass 430.0222229 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.30
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Chrysine A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9690 96.90%
Caco-2 + 0.6672 66.72%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8602 86.02%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.8198 81.98%
OATP1B3 inhibitior - 0.3786 37.86%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8311 83.11%
P-glycoprotein inhibitior - 0.5920 59.20%
P-glycoprotein substrate - 0.8740 87.40%
CYP3A4 substrate + 0.5296 52.96%
CYP2C9 substrate - 0.6146 61.46%
CYP2D6 substrate - 0.8938 89.38%
CYP3A4 inhibition - 0.9470 94.70%
CYP2C9 inhibition - 0.7881 78.81%
CYP2C19 inhibition - 0.7514 75.14%
CYP2D6 inhibition - 0.8915 89.15%
CYP1A2 inhibition - 0.5569 55.69%
CYP2C8 inhibition + 0.8439 84.39%
CYP inhibitory promiscuity - 0.7667 76.67%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6257 62.57%
Carcinogenicity (trinary) Non-required 0.4484 44.84%
Eye corrosion - 0.9828 98.28%
Eye irritation - 0.4772 47.72%
Skin irritation - 0.7218 72.18%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis - 0.5878 58.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5687 56.87%
Micronuclear + 0.6374 63.74%
Hepatotoxicity + 0.7281 72.81%
skin sensitisation - 0.8781 87.81%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5112 51.12%
Acute Oral Toxicity (c) III 0.5235 52.35%
Estrogen receptor binding + 0.9045 90.45%
Androgen receptor binding - 0.6474 64.74%
Thyroid receptor binding + 0.6449 64.49%
Glucocorticoid receptor binding + 0.8496 84.96%
Aromatase binding + 0.5788 57.88%
PPAR gamma + 0.8420 84.20%
Honey bee toxicity - 0.9399 93.99%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity + 0.9960 99.60%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.15% 83.82%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 95.93% 94.42%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.87% 99.15%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.68% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.15% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.70% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.51% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.50% 81.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.48% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.26% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 86.06% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.73% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.69% 95.56%
CHEMBL5905 Q04828 Aldo-keto reductase family 1 member C1 84.97% 91.79%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.76% 91.07%
CHEMBL3194 P02766 Transthyretin 83.81% 90.71%
CHEMBL5847 P52895 Aldo-keto reductase family 1 member C2 83.57% 92.50%
CHEMBL2535 P11166 Glucose transporter 83.33% 98.75%
CHEMBL2056 P21728 Dopamine D1 receptor 83.07% 91.00%
CHEMBL4208 P20618 Proteasome component C5 83.06% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.47% 96.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 82.14% 92.29%
CHEMBL1255126 O15151 Protein Mdm4 80.87% 90.20%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.42% 97.21%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.05% 87.67%

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 146684274
LOTUS LTS0065751
wikiData Q105167151