Flemichapparin C

Details

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Internal ID 140a934f-96e0-4df6-9ac6-26b797f6afaf
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Coumestans
IUPAC Name 16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-20-one
SMILES (Canonical) COC1=CC2=C(C=C1)C3=C(C4=CC5=C(C=C4O3)OCO5)C(=O)O2
SMILES (Isomeric) COC1=CC2=C(C=C1)C3=C(C4=CC5=C(C=C4O3)OCO5)C(=O)O2
InChI InChI=1S/C17H10O6/c1-19-8-2-3-9-11(4-8)23-17(18)15-10-5-13-14(21-7-20-13)6-12(10)22-16(9)15/h2-6H,7H2,1H3
InChI Key ZIZYKBRERUNPAU-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H10O6
Molecular Weight 310.26 g/mol
Exact Mass 310.04773803 g/mol
Topological Polar Surface Area (TPSA) 67.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3-Methoxy-8,9-methylenedioxycoumestan
SCHEMBL13692853
LMPK12090027
3862-34-8

2D Structure

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2D Structure of Flemichapparin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.6633 66.33%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7033 70.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9600 96.00%
OATP1B3 inhibitior + 0.9794 97.94%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5173 51.73%
P-glycoprotein inhibitior + 0.7569 75.69%
P-glycoprotein substrate - 0.8899 88.99%
CYP3A4 substrate - 0.5220 52.20%
CYP2C9 substrate - 0.8269 82.69%
CYP2D6 substrate - 0.8481 84.81%
CYP3A4 inhibition + 0.9004 90.04%
CYP2C9 inhibition + 0.8425 84.25%
CYP2C19 inhibition + 0.9523 95.23%
CYP2D6 inhibition + 0.9082 90.82%
CYP1A2 inhibition + 0.8955 89.55%
CYP2C8 inhibition - 0.8451 84.51%
CYP inhibitory promiscuity + 0.9030 90.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Warning 0.4486 44.86%
Eye corrosion - 0.9368 93.68%
Eye irritation - 0.5975 59.75%
Skin irritation - 0.6842 68.42%
Skin corrosion - 0.9680 96.80%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6034 60.34%
Micronuclear + 0.7874 78.74%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.6544 65.44%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6648 66.48%
Acute Oral Toxicity (c) III 0.7544 75.44%
Estrogen receptor binding + 0.9026 90.26%
Androgen receptor binding + 0.9005 90.05%
Thyroid receptor binding + 0.6578 65.78%
Glucocorticoid receptor binding + 0.9046 90.46%
Aromatase binding + 0.8225 82.25%
PPAR gamma + 0.8952 89.52%
Honey bee toxicity - 0.8431 84.31%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8657 86.57%

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 98.95% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.57% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.56% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.10% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.37% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.61% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.29% 92.62%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.98% 85.30%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.19% 94.00%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 90.87% 93.24%
CHEMBL1907 P15144 Aminopeptidase N 89.92% 93.31%
CHEMBL240 Q12809 HERG 89.86% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.70% 86.33%
CHEMBL2039 P27338 Monoamine oxidase B 89.19% 92.51%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.37% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.34% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.31% 89.00%
CHEMBL4208 P20618 Proteasome component C5 85.06% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 84.83% 94.73%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 83.97% 80.96%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.52% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.49% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.38% 96.67%
CHEMBL2535 P11166 Glucose transporter 81.77% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.27% 93.99%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.46% 100.00%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 80.00% 85.00%

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.
Abrus melanospermus subsp. melanospermus
Brachypterum scandens
Cicer arietinum
Deguelia scandens
Eysenhardtia polystachya
Flemingia chappar
Galega officinalis
Tephrosia purpurea

Cross-Links

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PubChem 11088179
NPASS NPC62074
LOTUS LTS0028051
wikiData Q104251051