Hinduchelin D

Details

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Internal ID 178cc516-1bf4-444f-b57a-d147e498ca16
Taxonomy Organoheterocyclic compounds > Azoles > Oxazoles > Phenyl-1,3-oxazoles
IUPAC Name 2-(2-hydroxy-3-methoxyphenyl)-5-methyl-N-(2-phenylethyl)-1,3-oxazole-4-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20N2O4/c1-13-17(19(24)21-12-11-14-7-4-3-5-8-14)22-20(26-13)15-9-6-10-16(25-2)18(15)23/h3-10,23H,11-12H2,1-2H3,(H,21,24)
InChI Key MDKMSZUTNDZRQG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20N2O4
Molecular Weight 352.40 g/mol
Exact Mass 352.14230712 g/mol
Topological Polar Surface Area (TPSA) 84.60 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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2-(2-hydroxy-3-methoxyphenyl)-5-methyl-N-(2-phenylethyl)-1,3-oxazole-4-carboxamide
RefChem:146437
2-(2-Hydroxy-3-methoxyphenyl)-5-methyl-N-(2-phenylethyl)-1,3-oxazole-4-carboximidate
CHEMBL4163595
CHEBI:209793

2D Structure

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2D Structure of Hinduchelin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9719 97.19%
Caco-2 - 0.6257 62.57%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7923 79.23%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.8930 89.30%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9237 92.37%
P-glycoprotein inhibitior + 0.7922 79.22%
P-glycoprotein substrate + 0.7881 78.81%
CYP3A4 substrate + 0.6253 62.53%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8636 86.36%
CYP3A4 inhibition + 0.6396 63.96%
CYP2C9 inhibition - 0.5547 55.47%
CYP2C19 inhibition + 0.5737 57.37%
CYP2D6 inhibition - 0.7468 74.68%
CYP1A2 inhibition + 0.5521 55.21%
CYP2C8 inhibition + 0.8721 87.21%
CYP inhibitory promiscuity + 0.7398 73.98%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6526 65.26%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9690 96.90%
Skin irritation - 0.8006 80.06%
Skin corrosion - 0.9413 94.13%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7051 70.51%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.6266 62.66%
skin sensitisation - 0.8902 89.02%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7674 76.74%
Acute Oral Toxicity (c) III 0.6773 67.73%
Estrogen receptor binding + 0.9041 90.41%
Androgen receptor binding + 0.6995 69.95%
Thyroid receptor binding + 0.5905 59.05%
Glucocorticoid receptor binding + 0.8638 86.38%
Aromatase binding + 0.7421 74.21%
PPAR gamma + 0.7443 74.43%
Honey bee toxicity - 0.8478 84.78%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.8462 84.62%

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
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 97.28% 95.72%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 96.52% 81.11%
CHEMBL1255126 O15151 Protein Mdm4 95.29% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.12% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.01% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.22% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.05% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.59% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.14% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.75% 96.00%
CHEMBL2535 P11166 Glucose transporter 89.02% 98.75%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.98% 87.67%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.65% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 88.62% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.86% 95.56%
CHEMBL5028 O14672 ADAM10 84.35% 97.50%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.34% 96.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.17% 91.11%

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 139590041
LOTUS LTS0217588
wikiData Q104171579