Isoplatydesmine

Details

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Internal ID 95341431-a009-41e6-85f9-b5b40f91be16
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Dihydrofuranoquinolines
IUPAC Name 2-(2-hydroxypropan-2-yl)-9-methyl-2,3-dihydrofuro[2,3-b]quinolin-4-one
SMILES (Canonical) CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O
SMILES (Isomeric) CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O
InChI InChI=1S/C15H17NO3/c1-15(2,18)12-8-10-13(17)9-6-4-5-7-11(9)16(3)14(10)19-12/h4-7,12,18H,8H2,1-3H3
InChI Key VLHROMVHVKMNLA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H17NO3
Molecular Weight 259.30 g/mol
Exact Mass 259.12084340 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.61
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL21394
2-(2-hydroxypropan-2-yl)-9-methyl-2,3-dihydrofuro[2,3-b]quinolin-4-one

2D Structure

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2D Structure of Isoplatydesmine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9714 97.14%
Caco-2 + 0.7702 77.02%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5385 53.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9444 94.44%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7534 75.34%
P-glycoprotein inhibitior - 0.9204 92.04%
P-glycoprotein substrate - 0.7996 79.96%
CYP3A4 substrate + 0.6040 60.40%
CYP2C9 substrate - 0.6189 61.89%
CYP2D6 substrate - 0.7964 79.64%
CYP3A4 inhibition - 0.9077 90.77%
CYP2C9 inhibition - 0.8274 82.74%
CYP2C19 inhibition - 0.6415 64.15%
CYP2D6 inhibition - 0.8342 83.42%
CYP1A2 inhibition + 0.7473 74.73%
CYP2C8 inhibition - 0.9023 90.23%
CYP inhibitory promiscuity - 0.8198 81.98%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4779 47.79%
Eye corrosion - 0.9902 99.02%
Eye irritation + 0.5292 52.92%
Skin irritation - 0.8137 81.37%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4687 46.87%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8536 85.36%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7827 78.27%
Acute Oral Toxicity (c) III 0.5862 58.62%
Estrogen receptor binding + 0.8221 82.21%
Androgen receptor binding + 0.5237 52.37%
Thyroid receptor binding + 0.5696 56.96%
Glucocorticoid receptor binding - 0.6512 65.12%
Aromatase binding + 0.5259 52.59%
PPAR gamma + 0.6281 62.81%
Honey bee toxicity - 0.9535 95.35%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.5078 50.78%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.54% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.45% 97.25%
CHEMBL2581 P07339 Cathepsin D 95.29% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.60% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.60% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.22% 91.11%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.49% 85.94%
CHEMBL3401 O75469 Pregnane X receptor 88.17% 94.73%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 88.08% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.81% 86.33%
CHEMBL3384 Q16512 Protein kinase N1 86.25% 80.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.14% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.25% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.76% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.46% 93.65%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.42% 100.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.36% 90.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.27% 96.09%

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.
Amyris diatrypa
Boronia pancheri
Haplophyllum patavinum
Melicope barbigera
Melicope semecarpifolia
Orixa japonica
Vepris nobilis
Zanthoxylum nitidum

Cross-Links

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PubChem 11219133
NPASS NPC12669
LOTUS LTS0255193
wikiData Q104403696