AH-1763 IIa

Details

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Internal ID ab269ecc-4c92-4d49-b139-1a1ef67e64ba
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 11-hydroxy-2-(3-hydroxybutan-2-yl)-5-methylnaphtho[2,3-h]chromene-4,7,12-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H18O6/c1-9-7-13-19(21(27)18-12(20(13)26)5-4-6-14(18)24)22-17(9)15(25)8-16(28-22)10(2)11(3)23/h4-8,10-11,23-24H,1-3H3
InChI Key ONHCPBOKJBCMAX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H18O6
Molecular Weight 378.40 g/mol
Exact Mass 378.11033829 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.07
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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AH-1763 IIa
11-Hydroxy-2-(3-hydroxybutan-2-yl)-5-methylnaphtho[2,3-h]chromene-4,7,12-trione

2D Structure

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2D Structure of AH-1763 IIa

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9709 97.09%
Caco-2 + 0.7293 72.93%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7959 79.59%
OATP2B1 inhibitior - 0.5702 57.02%
OATP1B1 inhibitior + 0.9077 90.77%
OATP1B3 inhibitior + 0.9738 97.38%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6698 66.98%
P-glycoprotein inhibitior - 0.6165 61.65%
P-glycoprotein substrate - 0.6952 69.52%
CYP3A4 substrate + 0.5287 52.87%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8372 83.72%
CYP3A4 inhibition - 0.8249 82.49%
CYP2C9 inhibition - 0.6230 62.30%
CYP2C19 inhibition - 0.8870 88.70%
CYP2D6 inhibition - 0.8828 88.28%
CYP1A2 inhibition + 0.9087 90.87%
CYP2C8 inhibition - 0.6980 69.80%
CYP inhibitory promiscuity - 0.7323 73.23%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.6689 66.89%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.8143 81.43%
Skin irritation - 0.6623 66.23%
Skin corrosion - 0.9737 97.37%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6204 62.04%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9322 93.22%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5588 55.88%
Acute Oral Toxicity (c) III 0.6393 63.93%
Estrogen receptor binding + 0.7748 77.48%
Androgen receptor binding + 0.7630 76.30%
Thyroid receptor binding - 0.5609 56.09%
Glucocorticoid receptor binding + 0.6939 69.39%
Aromatase binding + 0.6108 61.08%
PPAR gamma + 0.7049 70.49%
Honey bee toxicity - 0.8898 88.98%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.9297 92.97%

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
CHEMBL2581 P07339 Cathepsin D 99.18% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.83% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.53% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.66% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 96.29% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.05% 99.15%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.84% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.86% 99.23%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.39% 90.24%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.64% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.49% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.68% 94.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.51% 93.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.26% 100.00%
CHEMBL2535 P11166 Glucose transporter 83.28% 98.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.91% 96.67%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.42% 93.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.33% 90.71%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.61% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.37% 86.33%

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 10045185
LOTUS LTS0201462
wikiData Q77371812