haplophytin A

Details

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Internal ID 7d6ed968-cc2b-42b3-9906-914dac54287f
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Pyranoquinolines
IUPAC Name 10-methoxy-2,2-dimethyl-6H-pyrano[3,2-c]quinolin-5-one
SMILES (Canonical) CC1(C=CC2=C(O1)C3=C(C=CC=C3OC)NC2=O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C3=C(C=CC=C3OC)NC2=O)C
InChI InChI=1S/C15H15NO3/c1-15(2)8-7-9-13(19-15)12-10(16-14(9)17)5-4-6-11(12)18-3/h4-8H,1-3H3,(H,16,17)
InChI Key SMAYXCAPAZDLBX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H15NO3
Molecular Weight 257.28 g/mol
Exact Mass 257.10519334 g/mol
Topological Polar Surface Area (TPSA) 47.60 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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10-Methoxy-2,2-dimethyl-6H-pyrano[3,2-c]quinolin-5-one

2D Structure

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2D Structure of haplophytin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.6593 65.93%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6658 66.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9207 92.07%
OATP1B3 inhibitior + 0.9688 96.88%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5158 51.58%
P-glycoprotein inhibitior - 0.8921 89.21%
P-glycoprotein substrate - 0.7208 72.08%
CYP3A4 substrate + 0.5906 59.06%
CYP2C9 substrate - 0.6070 60.70%
CYP2D6 substrate - 0.8552 85.52%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.6651 66.51%
CYP2C19 inhibition + 0.5584 55.84%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition + 0.9107 91.07%
CYP2C8 inhibition - 0.6038 60.38%
CYP inhibitory promiscuity + 0.5679 56.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Danger 0.4491 44.91%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.9224 92.24%
Skin irritation - 0.8533 85.33%
Skin corrosion - 0.9657 96.57%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5276 52.76%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5650 56.50%
skin sensitisation - 0.8482 84.82%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.6471 64.71%
Acute Oral Toxicity (c) III 0.5517 55.17%
Estrogen receptor binding + 0.8719 87.19%
Androgen receptor binding + 0.5727 57.27%
Thyroid receptor binding + 0.6854 68.54%
Glucocorticoid receptor binding + 0.7583 75.83%
Aromatase binding + 0.8649 86.49%
PPAR gamma + 0.7855 78.55%
Honey bee toxicity - 0.8197 81.97%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.6841 68.41%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.77% 94.45%
CHEMBL2535 P11166 Glucose transporter 94.11% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.04% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.81% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.80% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.28% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.19% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 88.22% 90.20%
CHEMBL2581 P07339 Cathepsin D 86.71% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.89% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.65% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.42% 97.14%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.24% 85.30%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.69% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.08% 95.89%
CHEMBL1907 P15144 Aminopeptidase N 80.94% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.57% 89.00%

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.
Haplophyllum acutifolium

Cross-Links

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PubChem 12968471
LOTUS LTS0241403
wikiData Q105255805