Ismailin

Details

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Internal ID cb34da60-3712-4b22-b7b8-f59d31166fe9
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 4-hydroxycoumarins
IUPAC Name 5-hydroxy-2,3-bis(4-hydroxy-5-methyl-2-oxochromen-3-yl)-7-methylnaphthalene-1,4-dione
SMILES (Canonical) CC1=C2C(=CC=C1)OC(=O)C(=C2O)C3=C(C(=O)C4=C(C3=O)C=C(C=C4O)C)C5=C(C6=C(C=CC=C6OC5=O)C)O
SMILES (Isomeric) CC1=C2C(=CC=C1)OC(=O)C(=C2O)C3=C(C(=O)C4=C(C3=O)C=C(C=C4O)C)C5=C(C6=C(C=CC=C6OC5=O)C)O
InChI InChI=1S/C31H20O9/c1-12-10-15-21(16(32)11-12)29(36)23(25-28(35)20-14(3)7-5-9-18(20)40-31(25)38)22(26(15)33)24-27(34)19-13(2)6-4-8-17(19)39-30(24)37/h4-11,32,34-35H,1-3H3
InChI Key ANMHSKMVWXRFBM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C31H20O9
Molecular Weight 536.50 g/mol
Exact Mass 536.11073221 g/mol
Topological Polar Surface Area (TPSA) 147.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.93
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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NSC377682
NSC-377682

2D Structure

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2D Structure of Ismailin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 - 0.6502 65.02%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8523 85.23%
OATP2B1 inhibitior - 0.5597 55.97%
OATP1B1 inhibitior + 0.8967 89.67%
OATP1B3 inhibitior + 0.8895 88.95%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7594 75.94%
P-glycoprotein inhibitior - 0.4700 47.00%
P-glycoprotein substrate - 0.8832 88.32%
CYP3A4 substrate + 0.5320 53.20%
CYP2C9 substrate + 0.6404 64.04%
CYP2D6 substrate - 0.8871 88.71%
CYP3A4 inhibition - 0.8325 83.25%
CYP2C9 inhibition + 0.8415 84.15%
CYP2C19 inhibition - 0.5625 56.25%
CYP2D6 inhibition - 0.9488 94.88%
CYP1A2 inhibition - 0.8360 83.60%
CYP2C8 inhibition - 0.6072 60.72%
CYP inhibitory promiscuity + 0.6061 60.61%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9713 97.13%
Carcinogenicity (trinary) Danger 0.5927 59.27%
Eye corrosion - 0.9933 99.33%
Eye irritation - 0.6202 62.02%
Skin irritation - 0.6336 63.36%
Skin corrosion - 0.9634 96.34%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7059 70.59%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.8392 83.92%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4591 45.91%
Acute Oral Toxicity (c) III 0.4104 41.04%
Estrogen receptor binding + 0.8493 84.93%
Androgen receptor binding + 0.6406 64.06%
Thyroid receptor binding - 0.5397 53.97%
Glucocorticoid receptor binding + 0.7758 77.58%
Aromatase binding - 0.5225 52.25%
PPAR gamma + 0.8031 80.31%
Honey bee toxicity - 0.9396 93.96%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9938 99.38%

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 98.22% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.33% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.92% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.82% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.81% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 95.39% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 95.05% 91.49%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.86% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.67% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.81% 99.15%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.78% 96.21%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.49% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.72% 86.33%
CHEMBL240 Q12809 HERG 84.74% 89.76%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.11% 93.03%
CHEMBL1811 P34995 Prostanoid EP1 receptor 81.93% 95.71%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.85% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.15% 90.71%

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.
Diospyros ismailii
Diospyros maingayi

Cross-Links

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PubChem 135454728
LOTUS LTS0173230
wikiData Q104397041