Haplatine acetate

Details

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Internal ID d07d36f5-81b8-4c91-925d-d7e7a568e975
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Furanoquinolines
IUPAC Name 1-[(Z)-4-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxybut-2-en-2-yl]oxypropan-2-one
SMILES (Canonical) CC(=O)COC(=CCOC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)C
SMILES (Isomeric) CC(=O)CO/C(=C\COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)/C
InChI InChI=1S/C20H21NO6/c1-12(22)11-27-13(2)7-9-25-16-6-5-14-17(19(16)24-4)21-20-15(8-10-26-20)18(14)23-3/h5-8,10H,9,11H2,1-4H3/b13-7-
InChI Key DMUYUTJUTCOSQS-QPEQYQDCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H21NO6
Molecular Weight 371.40 g/mol
Exact Mass 371.13688739 g/mol
Topological Polar Surface Area (TPSA) 80.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.89
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Haplatine acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.6984 69.84%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6103 61.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9448 94.48%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9418 94.18%
P-glycoprotein inhibitior + 0.7874 78.74%
P-glycoprotein substrate - 0.6709 67.09%
CYP3A4 substrate + 0.5459 54.59%
CYP2C9 substrate - 0.7688 76.88%
CYP2D6 substrate - 0.7502 75.02%
CYP3A4 inhibition + 0.7351 73.51%
CYP2C9 inhibition - 0.6809 68.09%
CYP2C19 inhibition - 0.5892 58.92%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition + 0.7255 72.55%
CYP2C8 inhibition + 0.7078 70.78%
CYP inhibitory promiscuity + 0.7264 72.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5940 59.40%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.8319 83.19%
Skin irritation - 0.8298 82.98%
Skin corrosion - 0.9533 95.33%
Ames mutagenesis - 0.5054 50.54%
Human Ether-a-go-go-Related Gene inhibition + 0.9375 93.75%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.7769 77.69%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4731 47.31%
Acute Oral Toxicity (c) III 0.6054 60.54%
Estrogen receptor binding + 0.7605 76.05%
Androgen receptor binding + 0.7630 76.30%
Thyroid receptor binding + 0.7550 75.50%
Glucocorticoid receptor binding + 0.9032 90.32%
Aromatase binding + 0.7096 70.96%
PPAR gamma + 0.7931 79.31%
Honey bee toxicity - 0.8918 89.18%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.8751 87.51%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.99% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.41% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.41% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.65% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.26% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.55% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 87.28% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.45% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.07% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.35% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.35% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 81.46% 91.49%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.32% 96.90%
CHEMBL5747 Q92793 CREB-binding protein 80.83% 95.12%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.31% 96.67%
CHEMBL2535 P11166 Glucose transporter 80.25% 98.75%

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 obtusifolium

Cross-Links

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PubChem 163184397
LOTUS LTS0131390
wikiData Q104985344