Haplophylline

Details

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Internal ID 5764fe51-e18e-4a7f-9b32-7c0612e1369c
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Pyranoquinolines
IUPAC Name (2,2-dimethyl-5-oxopyrano[3,2-c]quinolin-6-yl)methyl 3-methylbut-2-enoate
SMILES (Canonical) CC(=CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C=CC(O3)(C)C)C
SMILES (Isomeric) CC(=CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C=CC(O3)(C)C)C
InChI InChI=1S/C20H21NO4/c1-13(2)11-17(22)24-12-21-16-8-6-5-7-14(16)18-15(19(21)23)9-10-20(3,4)25-18/h5-11H,12H2,1-4H3
InChI Key HUEQNVBOFCAFSJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H21NO4
Molecular Weight 339.40 g/mol
Exact Mass 339.14705815 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.65
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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R4M3VBY2ZP
93710-20-4
2-Butenoic acid, 3-methyl-, (2,2-dimethyl-5-oxo-2H-pyrano(3,2-C)quinolin-6(5H)-yl)methyl ester
UNII-R4M3VBY2ZP
HUEQNVBOFCAFSJ-UHFFFAOYSA-N
Q27287791
(2,2-Dimethyl-5-oxo-2H-pyrano[3,2-c]quinolin-6(5H)-yl)methyl 3-methyl-2-butenoate #

2D Structure

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2D Structure of Haplophylline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9343 93.43%
Caco-2 + 0.8186 81.86%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5251 52.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8841 88.41%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9066 90.66%
BSEP inhibitior + 0.7257 72.57%
P-glycoprotein inhibitior + 0.6150 61.50%
P-glycoprotein substrate - 0.6418 64.18%
CYP3A4 substrate + 0.6875 68.75%
CYP2C9 substrate - 0.5956 59.56%
CYP2D6 substrate - 0.8907 89.07%
CYP3A4 inhibition + 0.7263 72.63%
CYP2C9 inhibition - 0.5551 55.51%
CYP2C19 inhibition + 0.6607 66.07%
CYP2D6 inhibition - 0.8537 85.37%
CYP1A2 inhibition + 0.6775 67.75%
CYP2C8 inhibition - 0.6019 60.19%
CYP inhibitory promiscuity + 0.8548 85.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4591 45.91%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.7069 70.69%
Skin irritation - 0.8152 81.52%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7232 72.32%
Micronuclear + 0.7574 75.74%
Hepatotoxicity + 0.5499 54.99%
skin sensitisation - 0.8407 84.07%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6476 64.76%
Acute Oral Toxicity (c) III 0.6705 67.05%
Estrogen receptor binding + 0.8798 87.98%
Androgen receptor binding + 0.6712 67.12%
Thyroid receptor binding + 0.7195 71.95%
Glucocorticoid receptor binding + 0.6214 62.14%
Aromatase binding + 0.5323 53.23%
PPAR gamma + 0.5685 56.85%
Honey bee toxicity - 0.8068 80.68%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9685 96.85%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.23% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.70% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.35% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.26% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.31% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.07% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.44% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.24% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 87.99% 94.73%
CHEMBL255 P29275 Adenosine A2b receptor 86.40% 98.59%
CHEMBL221 P23219 Cyclooxygenase-1 84.52% 90.17%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.41% 95.71%
CHEMBL5028 O14672 ADAM10 80.95% 97.50%

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 suaveolens
Myrtopsis macrocarpa

Cross-Links

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PubChem 629670
LOTUS LTS0185160
wikiData Q27287791