Hinduchelin C

Details

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Internal ID aef91efb-906b-4afd-8b8e-c4144add8473
Taxonomy Organoheterocyclic compounds > Azoles > Oxazoles > Phenyl-1,3-oxazoles
IUPAC Name 2-(2-hydroxy-3-methoxyphenyl)-N-[2-(2-hydroxyphenyl)ethyl]-5-methyl-1,3-oxazole-4-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20N2O5/c1-12-17(19(25)21-11-10-13-6-3-4-8-15(13)23)22-20(27-12)14-7-5-9-16(26-2)18(14)24/h3-9,23-24H,10-11H2,1-2H3,(H,21,25)
InChI Key YUSPGCFRDYKBJM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20N2O5
Molecular Weight 368.40 g/mol
Exact Mass 368.13722174 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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CHEMBL4174276

2D Structure

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2D Structure of Hinduchelin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9425 94.25%
Caco-2 - 0.6096 60.96%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7941 79.41%
OATP2B1 inhibitior - 0.7098 70.98%
OATP1B1 inhibitior + 0.9131 91.31%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9367 93.67%
P-glycoprotein inhibitior + 0.7743 77.43%
P-glycoprotein substrate + 0.7490 74.90%
CYP3A4 substrate + 0.6338 63.38%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8636 86.36%
CYP3A4 inhibition + 0.6568 65.68%
CYP2C9 inhibition - 0.5578 55.78%
CYP2C19 inhibition + 0.5763 57.63%
CYP2D6 inhibition - 0.7116 71.16%
CYP1A2 inhibition + 0.5307 53.07%
CYP2C8 inhibition + 0.7847 78.47%
CYP inhibitory promiscuity + 0.7937 79.37%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6662 66.62%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9653 96.53%
Skin irritation - 0.7879 78.79%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7660 76.60%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5552 55.52%
skin sensitisation - 0.8893 88.93%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6680 66.80%
Acute Oral Toxicity (c) III 0.6800 68.00%
Estrogen receptor binding + 0.9093 90.93%
Androgen receptor binding + 0.6813 68.13%
Thyroid receptor binding + 0.6321 63.21%
Glucocorticoid receptor binding + 0.8456 84.56%
Aromatase binding + 0.7532 75.32%
PPAR gamma + 0.7046 70.46%
Honey bee toxicity - 0.8440 84.40%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.8042 80.42%

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 95.13% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.84% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.65% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 93.81% 90.20%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 93.69% 81.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.89% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.88% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.19% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.14% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.11% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 90.41% 94.73%
CHEMBL2535 P11166 Glucose transporter 89.94% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.29% 95.56%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 87.38% 95.72%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.38% 87.67%
CHEMBL5028 O14672 ADAM10 81.22% 97.50%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.77% 95.50%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 80.01% 96.39%

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 139590040
LOTUS LTS0275985
wikiData Q104202109