Gladiatoside A1

Details

Top
Internal ID 2abe5f01-71d1-4e6d-81ee-da52d1cc2d54
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name [6-[3-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] 2-methoxybenzoate
SMILES (Canonical) CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)OC(=O)C6=CC=CC=C6OC)O)O)C7=CC=C(C=C7)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)OC(=O)C6=CC=CC=C6OC)O)O)C7=CC=C(C=C7)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)O)O
InChI InChI=1S/C47H56O26/c1-16-28(51)32(55)36(59)44(65-16)64-15-26-30(53)34(57)42(73-46-37(60)33(56)29(52)25(14-48)69-46)47(70-26)72-41-31(54)27-22(50)12-20(13-24(27)68-40(41)18-8-10-19(49)11-9-18)67-45-38(61)35(58)39(17(2)66-45)71-43(62)21-6-4-5-7-23(21)63-3/h4-13,16-17,25-26,28-30,32-39,42,44-53,55-61H,14-15H2,1-3H3
InChI Key OXADVNUEZRYSAH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C47H56O26
Molecular Weight 1036.90 g/mol
Exact Mass 1036.30598189 g/mol
Topological Polar Surface Area (TPSA) 399.00 Ų
XlogP -1.60
Atomic LogP (AlogP) -3.19
H-Bond Acceptor 26
H-Bond Donor 13
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Gladiatoside A1

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6454 64.54%
Caco-2 - 0.8716 87.16%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.5304 53.04%
OATP2B1 inhibitior - 0.7199 71.99%
OATP1B1 inhibitior + 0.8669 86.69%
OATP1B3 inhibitior + 0.9682 96.82%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9412 94.12%
P-glycoprotein inhibitior + 0.7257 72.57%
P-glycoprotein substrate + 0.7472 74.72%
CYP3A4 substrate + 0.7049 70.49%
CYP2C9 substrate - 0.6753 67.53%
CYP2D6 substrate - 0.8653 86.53%
CYP3A4 inhibition - 0.9560 95.60%
CYP2C9 inhibition - 0.9176 91.76%
CYP2C19 inhibition - 0.9401 94.01%
CYP2D6 inhibition - 0.9681 96.81%
CYP1A2 inhibition - 0.9381 93.81%
CYP2C8 inhibition + 0.8544 85.44%
CYP inhibitory promiscuity - 0.8513 85.13%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6895 68.95%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9016 90.16%
Skin irritation - 0.8634 86.34%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8138 81.38%
Micronuclear + 0.6333 63.33%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.9325 93.25%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8060 80.60%
Acute Oral Toxicity (c) III 0.6579 65.79%
Estrogen receptor binding + 0.8035 80.35%
Androgen receptor binding + 0.6617 66.17%
Thyroid receptor binding + 0.5859 58.59%
Glucocorticoid receptor binding + 0.7114 71.14%
Aromatase binding + 0.5256 52.56%
PPAR gamma + 0.7915 79.15%
Honey bee toxicity - 0.6450 64.50%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7925 79.25%

Targets

Top

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 99.62% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.39% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.87% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.64% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.51% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.99% 89.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 95.99% 97.36%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.57% 96.09%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 91.57% 95.64%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.30% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.12% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.12% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 88.02% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.95% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 86.84% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.13% 99.15%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.01% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.15% 97.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.29% 96.00%
CHEMBL4530 P00488 Coagulation factor XIII 82.31% 96.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.99% 95.78%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.70% 96.21%

Plants that contains it

Top
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.
Canavalia gladiata

Cross-Links

Top
PubChem 85229862
LOTUS LTS0239796
wikiData Q105202442