Hippacine

Details

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Internal ID d482e302-8cf9-4d05-930d-f484f2f358e7
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Phenanthridines and derivatives
IUPAC Name 4,5-dihydroxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(15),2,4,6,10,12(16),13-heptaen-8-one
SMILES (Canonical) C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O
SMILES (Isomeric) C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O
InChI InChI=1S/C15H9NO3/c17-12-6-10-9-3-1-2-8-4-5-16(14(8)9)15(19)11(10)7-13(12)18/h1-7,17-18H
InChI Key KLZMKXANTDISDA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H9NO3
Molecular Weight 251.24 g/mol
Exact Mass 251.058243149 g/mol
Topological Polar Surface Area (TPSA) 62.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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11013-98-2

2D Structure

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2D Structure of Hippacine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9732 97.32%
Caco-2 + 0.7739 77.39%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7045 70.45%
OATP2B1 inhibitior - 0.7190 71.90%
OATP1B1 inhibitior + 0.9522 95.22%
OATP1B3 inhibitior + 0.9520 95.20%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8697 86.97%
BSEP inhibitior - 0.8151 81.51%
P-glycoprotein inhibitior - 0.9411 94.11%
P-glycoprotein substrate - 0.9448 94.48%
CYP3A4 substrate - 0.5502 55.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8438 84.38%
CYP3A4 inhibition - 0.8137 81.37%
CYP2C9 inhibition - 0.8483 84.83%
CYP2C19 inhibition - 0.8700 87.00%
CYP2D6 inhibition - 0.7450 74.50%
CYP1A2 inhibition + 0.9148 91.48%
CYP2C8 inhibition - 0.8648 86.48%
CYP inhibitory promiscuity - 0.6676 66.76%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4970 49.70%
Eye corrosion - 0.9900 99.00%
Eye irritation + 0.9248 92.48%
Skin irritation - 0.7359 73.59%
Skin corrosion - 0.9594 95.94%
Ames mutagenesis + 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9092 90.92%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6751 67.51%
skin sensitisation - 0.8425 84.25%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6596 65.96%
Acute Oral Toxicity (c) II 0.4992 49.92%
Estrogen receptor binding + 0.7993 79.93%
Androgen receptor binding + 0.5656 56.56%
Thyroid receptor binding + 0.7692 76.92%
Glucocorticoid receptor binding + 0.9769 97.69%
Aromatase binding + 0.8003 80.03%
PPAR gamma + 0.8852 88.52%
Honey bee toxicity - 0.9065 90.65%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.6605 66.05%

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 95.56% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 93.48% 91.49%
CHEMBL2581 P07339 Cathepsin D 93.40% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.69% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.43% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.34% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.30% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.63% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.08% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.90% 93.99%

Cross-Links

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PubChem 10015025
NPASS NPC173741
LOTUS LTS0187415
wikiData Q105142878