Phaseolorin C

Details

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Internal ID 324e6547-60ae-4070-8fe7-280894ddf6f6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name [(2S,3R)-2-[(2S)-5-hydroxy-2-(hydroxymethyl)-4-oxo-3H-chromen-2-yl]-5-oxooxolan-3-yl]methyl acetate
SMILES (Canonical) CC(=O)OCC1CC(=O)OC1C2(CC(=O)C3=C(C=CC=C3O2)O)CO
SMILES (Isomeric) CC(=O)OC[C@H]1CC(=O)O[C@@H]1[C@]2(CC(=O)C3=C(C=CC=C3O2)O)CO
InChI InChI=1S/C17H18O8/c1-9(19)23-7-10-5-14(22)24-16(10)17(8-18)6-12(21)15-11(20)3-2-4-13(15)25-17/h2-4,10,16,18,20H,5-8H2,1H3/t10-,16+,17+/m1/s1
InChI Key DEDISAPWHIUADD-YKJXYISPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O8
Molecular Weight 350.30 g/mol
Exact Mass 350.10016753 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.58
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phaseolorin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9234 92.34%
Caco-2 - 0.5575 55.75%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8460 84.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8585 85.85%
OATP1B3 inhibitior + 0.9265 92.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6065 60.65%
P-glycoprotein inhibitior - 0.7290 72.90%
P-glycoprotein substrate - 0.7101 71.01%
CYP3A4 substrate + 0.6295 62.95%
CYP2C9 substrate + 0.6313 63.13%
CYP2D6 substrate - 0.8533 85.33%
CYP3A4 inhibition - 0.9076 90.76%
CYP2C9 inhibition - 0.6905 69.05%
CYP2C19 inhibition - 0.7061 70.61%
CYP2D6 inhibition - 0.9500 95.00%
CYP1A2 inhibition - 0.8844 88.44%
CYP2C8 inhibition + 0.4647 46.47%
CYP inhibitory promiscuity - 0.6908 69.08%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5628 56.28%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.8239 82.39%
Skin irritation - 0.8197 81.97%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis - 0.5137 51.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6315 63.15%
Micronuclear - 0.5867 58.67%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8860 88.60%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7590 75.90%
Acute Oral Toxicity (c) III 0.4579 45.79%
Estrogen receptor binding + 0.7909 79.09%
Androgen receptor binding + 0.7118 71.18%
Thyroid receptor binding - 0.5846 58.46%
Glucocorticoid receptor binding + 0.5495 54.95%
Aromatase binding - 0.6271 62.71%
PPAR gamma + 0.6534 65.34%
Honey bee toxicity - 0.8909 89.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5150 51.50%
Fish aquatic toxicity + 0.9340 93.40%

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 98.98% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.38% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.31% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.51% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.93% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 94.54% 97.79%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.97% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.50% 95.56%
CHEMBL299 P17252 Protein kinase C alpha 90.76% 98.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.96% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.06% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.74% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.17% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.55% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.61% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 82.73% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.68% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 81.52% 94.73%
CHEMBL5028 O14672 ADAM10 80.99% 97.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.57% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146682907
LOTUS LTS0068584
wikiData Q104977107