methyl 2-[(2S,3R,4R,5R,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]-2-[10-[(2S,4R,5S,6S)-4-(dimethylamino)-5-[(2S,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4,6-dimethyloxan-2-yl]-2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-4,7,12-trioxonaphtho[2,3-h]chromen-5-yl]-2-hydroxyacetate

Details

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Internal ID 9dbcabd9-7780-485f-98ae-ab412e15412e
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones > Naphthopyranone glycosides
IUPAC Name methyl 2-[(2S,3R,4R,5R,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]-2-[10-[(2S,4R,5S,6S)-4-(dimethylamino)-5-[(2S,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4,6-dimethyloxan-2-yl]-2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-4,7,12-trioxonaphtho[2,3-h]chromen-5-yl]-2-hydroxyacetate
SMILES (Canonical) CC1C(C(CC(O1)OC2C(OC(CC2(C)N(C)C)C3=C(C4=C(C=C3)C(=O)C5=CC(=C6C(=O)C=C(OC6=C5C4=O)C7(C(O7)C)C)C(C8C(C(C(C(O8)C)O)OC)O)(C(=O)OC)O)O)C)OC)O
SMILES (Isomeric) C[C@@H]1[C@@H]([C@H](C[C@@H](O1)O[C@@H]2[C@@H](O[C@@H](C[C@@]2(C)N(C)C)C3=C(C4=C(C=C3)C(=O)C5=CC(=C6C(=O)C=C(OC6=C5C4=O)C7(C(O7)C)C)C([C@@H]8[C@@H]([C@@H]([C@@H]([C@@H](O8)C)O)OC)O)(C(=O)OC)O)O)C)OC)O
InChI InChI=1S/C47H59NO18/c1-18-34(50)27(58-9)16-30(62-18)65-42-20(3)61-28(17-45(42,5)48(7)8)22-12-13-23-31(37(22)53)38(54)32-24(36(23)52)14-25(33-26(49)15-29(64-40(32)33)46(6)21(4)66-46)47(57,44(56)60-11)43-39(55)41(59-10)35(51)19(2)63-43/h12-15,18-21,27-28,30,34-35,39,41-43,50-51,53,55,57H,16-17H2,1-11H3/t18-,19+,20+,21?,27+,28+,30+,34+,35-,39-,41-,42-,43+,45-,46?,47?/m1/s1
InChI Key FAGGWQMBDCZCOI-CHBSWCIFSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C47H59NO18
Molecular Weight 926.00 g/mol
Exact Mass 925.37321403 g/mol
Topological Polar Surface Area (TPSA) 259.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 19
H-Bond Donor 5
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 2-[(2S,3R,4R,5R,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]-2-[10-[(2S,4R,5S,6S)-4-(dimethylamino)-5-[(2S,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4,6-dimethyloxan-2-yl]-2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-4,7,12-trioxonaphtho[2,3-h]chromen-5-yl]-2-hydroxyacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7301 73.01%
Caco-2 - 0.8607 86.07%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Lysosomes 0.3581 35.81%
OATP2B1 inhibitior - 0.7122 71.22%
OATP1B1 inhibitior + 0.8214 82.14%
OATP1B3 inhibitior + 0.9158 91.58%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9184 91.84%
P-glycoprotein inhibitior + 0.7467 74.67%
P-glycoprotein substrate + 0.8556 85.56%
CYP3A4 substrate + 0.7533 75.33%
CYP2C9 substrate - 0.6206 62.06%
CYP2D6 substrate - 0.8390 83.90%
CYP3A4 inhibition + 0.5305 53.05%
CYP2C9 inhibition - 0.7764 77.64%
CYP2C19 inhibition - 0.7928 79.28%
CYP2D6 inhibition - 0.7953 79.53%
CYP1A2 inhibition - 0.5153 51.53%
CYP2C8 inhibition + 0.7429 74.29%
CYP inhibitory promiscuity - 0.8168 81.68%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5232 52.32%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9036 90.36%
Skin irritation - 0.7910 79.10%
Skin corrosion - 0.9260 92.60%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3757 37.57%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8814 88.14%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.6897 68.97%
Acute Oral Toxicity (c) III 0.5471 54.71%
Estrogen receptor binding + 0.8003 80.03%
Androgen receptor binding + 0.7522 75.22%
Thyroid receptor binding + 0.6113 61.13%
Glucocorticoid receptor binding + 0.8054 80.54%
Aromatase binding + 0.6490 64.90%
PPAR gamma + 0.7977 79.77%
Honey bee toxicity - 0.6438 64.38%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9274 92.74%

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 99.74% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.36% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 98.27% 89.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 95.68% 95.64%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 94.41% 97.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.08% 96.77%
CHEMBL5608 Q16288 NT-3 growth factor receptor 94.08% 95.89%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.75% 96.38%
CHEMBL240 Q12809 HERG 93.36% 89.76%
CHEMBL340 P08684 Cytochrome P450 3A4 93.32% 91.19%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 92.38% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.14% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.00% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.80% 99.23%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 90.76% 91.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.55% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.67% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.18% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.38% 97.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 87.99% 85.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.79% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.08% 100.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 85.79% 96.21%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.78% 100.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.66% 96.67%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 85.16% 96.90%
CHEMBL5408 Q9UHD2 Serine/threonine-protein kinase TBK1 85.02% 90.48%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.58% 92.88%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.79% 97.28%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.18% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.97% 99.17%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.88% 94.42%
CHEMBL1871 P10275 Androgen Receptor 81.24% 96.43%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.40% 90.71%

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 129628327
LOTUS LTS0094721
wikiData Q104992243