[(10Z,12S,13R,14S,16S)-7,14-dihydroxy-6,10,12,16-tetramethyl-2,9,15,21-tetraoxo-20-oxa-18-azatetracyclo[14.3.1.14,19.03,8]henicosa-1(19),3,5,7,10-pentaen-13-yl] 3-hydroxy-6-[(4-hydroxy-7-methoxy-2-oxochromen-3-yl)carbamoyl]-4-[(2S,4R,5S,6S)-5-methoxy-4,6-dimethyl-4-nitrosooxan-2-yl]oxypyridine-2-carboxylate

Details

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Internal ID 55fd64a1-03a6-41bd-82f9-e5b333801790
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 4-hydroxycoumarins
IUPAC Name [(10Z,12S,13R,14S,16S)-7,14-dihydroxy-6,10,12,16-tetramethyl-2,9,15,21-tetraoxo-20-oxa-18-azatetracyclo[14.3.1.14,19.03,8]henicosa-1(19),3,5,7,10-pentaen-13-yl] 3-hydroxy-6-[(4-hydroxy-7-methoxy-2-oxochromen-3-yl)carbamoyl]-4-[(2S,4R,5S,6S)-5-methoxy-4,6-dimethyl-4-nitrosooxan-2-yl]oxypyridine-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C48H46N4O19/c1-17-11-19(3)40(39(59)42(60)48(6)16-49-30-36(56)23-12-18(2)34(54)29(33(17)53)28(23)38(58)41(30)71-48)70-46(63)32-37(57)26(68-27-15-47(5,52-64)43(66-8)20(4)67-27)14-24(50-32)44(61)51-31-35(55)22-10-9-21(65-7)13-25(22)69-45(31)62/h9-14,19-20,27,39-40,43,49,54-55,57,59H,15-16H2,1-8H3,(H,51,61)/b17-11-/t19-,20-,27-,39-,40+,43+,47+,48-/m0/s1
InChI Key YOBDUGOCRYXTGC-KUIBHZFESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C48H46N4O19
Molecular Weight 982.90 g/mol
Exact Mass 982.27562525 g/mol
Topological Polar Surface Area (TPSA) 331.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 22
H-Bond Donor 6
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(10Z,12S,13R,14S,16S)-7,14-dihydroxy-6,10,12,16-tetramethyl-2,9,15,21-tetraoxo-20-oxa-18-azatetracyclo[14.3.1.14,19.03,8]henicosa-1(19),3,5,7,10-pentaen-13-yl] 3-hydroxy-6-[(4-hydroxy-7-methoxy-2-oxochromen-3-yl)carbamoyl]-4-[(2S,4R,5S,6S)-5-methoxy-4,6-dimethyl-4-nitrosooxan-2-yl]oxypyridine-2-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7806 78.06%
Caco-2 - 0.8572 85.72%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Plasma membrane 0.3751 37.51%
OATP2B1 inhibitior - 0.5762 57.62%
OATP1B1 inhibitior + 0.8075 80.75%
OATP1B3 inhibitior + 0.9340 93.40%
MATE1 inhibitior - 0.8100 81.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9146 91.46%
P-glycoprotein inhibitior + 0.7537 75.37%
P-glycoprotein substrate + 0.8432 84.32%
CYP3A4 substrate + 0.7597 75.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8570 85.70%
CYP3A4 inhibition - 0.7466 74.66%
CYP2C9 inhibition - 0.6483 64.83%
CYP2C19 inhibition - 0.6479 64.79%
CYP2D6 inhibition - 0.8790 87.90%
CYP1A2 inhibition - 0.7233 72.33%
CYP2C8 inhibition + 0.8244 82.44%
CYP inhibitory promiscuity - 0.6215 62.15%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.4830 48.30%
Eye corrosion - 0.9806 98.06%
Eye irritation - 0.9023 90.23%
Skin irritation - 0.7615 76.15%
Skin corrosion - 0.9233 92.33%
Ames mutagenesis - 0.5054 50.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6542 65.42%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5444 54.44%
skin sensitisation - 0.8398 83.98%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7966 79.66%
Acute Oral Toxicity (c) III 0.5854 58.54%
Estrogen receptor binding + 0.7942 79.42%
Androgen receptor binding + 0.7867 78.67%
Thyroid receptor binding + 0.6308 63.08%
Glucocorticoid receptor binding + 0.7229 72.29%
Aromatase binding + 0.6957 69.57%
PPAR gamma + 0.7721 77.21%
Honey bee toxicity - 0.6281 62.81%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5247 52.47%
Fish aquatic toxicity + 0.8942 89.42%

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 99.80% 91.11%
CHEMBL240 Q12809 HERG 99.74% 89.76%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.63% 94.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 96.34% 96.21%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 96.10% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.57% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 95.24% 91.49%
CHEMBL4530 P00488 Coagulation factor XIII 94.12% 96.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 93.88% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.50% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.16% 94.45%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 93.11% 81.11%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 92.21% 94.67%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 91.82% 96.47%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.72% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.71% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.69% 95.89%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 90.67% 96.00%
CHEMBL4208 P20618 Proteasome component C5 89.99% 90.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.55% 92.94%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 89.19% 96.67%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.19% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 89.10% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.98% 97.09%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 84.80% 83.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 84.49% 97.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.22% 91.07%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.17% 90.71%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.34% 96.90%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.92% 93.65%
CHEMBL1741221 Q9Y4P1 Cysteine protease ATG4B 82.89% 87.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.83% 99.17%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.64% 100.00%
CHEMBL2581 P07339 Cathepsin D 82.19% 98.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.44% 92.29%
CHEMBL340 P08684 Cytochrome P450 3A4 81.07% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.28% 92.62%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.19% 92.67%

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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Cross-Links

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PubChem 101633941
LOTUS LTS0039381
wikiData Q105351212