Hinduchelin B

Details

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Internal ID aa053a94-0534-45f0-a06d-1e8e2902be73
Taxonomy Organoheterocyclic compounds > Azoles > Oxazoles > Phenyl-1,3-oxazoles
IUPAC Name 2-(2,3-dimethoxyphenyl)-N-[2-(2-hydroxyphenyl)ethyl]-5-methyl-1,3-oxazole-4-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22N2O5/c1-13-18(20(25)22-12-11-14-7-4-5-9-16(14)24)23-21(28-13)15-8-6-10-17(26-2)19(15)27-3/h4-10,24H,11-12H2,1-3H3,(H,22,25)
InChI Key JAOSYQCRISHFFL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22N2O5
Molecular Weight 382.40 g/mol
Exact Mass 382.15287181 g/mol
Topological Polar Surface Area (TPSA) 93.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.35
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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CHEMBL4167772

2D Structure

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2D Structure of Hinduchelin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9292 92.92%
Caco-2 + 0.5090 50.90%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7759 77.59%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9140 91.40%
OATP1B3 inhibitior + 0.9328 93.28%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9286 92.86%
P-glycoprotein inhibitior + 0.8483 84.83%
P-glycoprotein substrate + 0.7288 72.88%
CYP3A4 substrate + 0.6357 63.57%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8636 86.36%
CYP3A4 inhibition + 0.8190 81.90%
CYP2C9 inhibition - 0.5863 58.63%
CYP2C19 inhibition + 0.5467 54.67%
CYP2D6 inhibition - 0.7296 72.96%
CYP1A2 inhibition + 0.5061 50.61%
CYP2C8 inhibition + 0.7826 78.26%
CYP inhibitory promiscuity + 0.7997 79.97%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6539 65.39%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9754 97.54%
Skin irritation - 0.7896 78.96%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8005 80.05%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.5177 51.77%
skin sensitisation - 0.8914 89.14%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6062 60.62%
Acute Oral Toxicity (c) III 0.6629 66.29%
Estrogen receptor binding + 0.8709 87.09%
Androgen receptor binding + 0.6690 66.90%
Thyroid receptor binding + 0.6940 69.40%
Glucocorticoid receptor binding + 0.8531 85.31%
Aromatase binding + 0.7268 72.68%
PPAR gamma + 0.7193 71.93%
Honey bee toxicity - 0.8472 84.72%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.7948 79.48%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.76% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.67% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 94.47% 90.20%
CHEMBL2535 P11166 Glucose transporter 93.49% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.36% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.76% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.20% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.19% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.95% 91.11%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 91.30% 81.11%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 89.97% 95.72%
CHEMBL3401 O75469 Pregnane X receptor 89.45% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.94% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.65% 98.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.92% 87.67%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 83.33% 95.39%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.39% 96.39%
CHEMBL5028 O14672 ADAM10 81.42% 97.50%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.61% 96.67%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.45% 99.15%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 139590039
LOTUS LTS0224411
wikiData Q104169333