3-O-beta-D-Glucopyranosylandrographolide

Details

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Internal ID 746bdb2c-3ef1-41fd-be52-28a1f9102885
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (3E,4S)-3-[2-[(1R,4aS,5R,6R,8aS)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-4-hydroxyoxolan-2-one
SMILES (Canonical) CC12CCC(C(C1CCC(=C)C2CC=C3C(COC3=O)O)(C)CO)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) C[C@@]12CC[C@H]([C@@]([C@H]1CCC(=C)[C@H]2C/C=C/3\[C@@H](COC3=O)O)(C)CO)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C26H40O10/c1-13-4-7-18-25(2,15(13)6-5-14-16(29)11-34-23(14)33)9-8-19(26(18,3)12-28)36-24-22(32)21(31)20(30)17(10-27)35-24/h5,15-22,24,27-32H,1,4,6-12H2,2-3H3/b14-5+/t15-,16-,17-,18+,19-,20-,21+,22-,24+,25+,26+/m1/s1
InChI Key ZWUABKNXVCUVCG-HHPBHMTBSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C26H40O10
Molecular Weight 512.60 g/mol
Exact Mass 512.26214747 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.21
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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869384-84-9
Compound NP-018050
CHEMBL472835
CHEBI:167804
AKOS040734197
NCGC00385288-01
(3E,4S)-3-[2-[(1R,4aS,5R,6R,8aS)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-4-hydroxyoxolan-2-one
NCGC00385288-01_C26H40O10_(1R,2R,4aS,5R,8aS)-1-(Hydroxymethyl)-5-{(2E)-2-[(4S)-4-hydroxy-2-oxodihydro-3(2H)-furanylidene]ethyl}-1,4a-dimethyl-6-methylenedecahydro-2-naphthalenyl beta-D-glucopyranoside

2D Structure

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2D Structure of 3-O-beta-D-Glucopyranosylandrographolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7469 74.69%
Caco-2 - 0.8292 82.92%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7735 77.35%
OATP2B1 inhibitior - 0.5851 58.51%
OATP1B1 inhibitior + 0.8914 89.14%
OATP1B3 inhibitior + 0.9273 92.73%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5330 53.30%
P-glycoprotein inhibitior - 0.5334 53.34%
P-glycoprotein substrate - 0.7060 70.60%
CYP3A4 substrate + 0.7173 71.73%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8853 88.53%
CYP3A4 inhibition - 0.9013 90.13%
CYP2C9 inhibition - 0.9158 91.58%
CYP2C19 inhibition - 0.9084 90.84%
CYP2D6 inhibition - 0.9256 92.56%
CYP1A2 inhibition - 0.8918 89.18%
CYP2C8 inhibition + 0.4865 48.65%
CYP inhibitory promiscuity - 0.9396 93.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6268 62.68%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9364 93.64%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis - 0.5670 56.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6804 68.04%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.7091 70.91%
skin sensitisation - 0.9025 90.25%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.8037 80.37%
Acute Oral Toxicity (c) I 0.6455 64.55%
Estrogen receptor binding + 0.7158 71.58%
Androgen receptor binding + 0.7710 77.10%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5731 57.31%
Aromatase binding + 0.6809 68.09%
PPAR gamma + 0.6458 64.58%
Honey bee toxicity - 0.7178 71.78%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9678 96.78%

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 96.56% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.01% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 91.48% 83.82%
CHEMBL2581 P07339 Cathepsin D 89.95% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.44% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.27% 100.00%
CHEMBL220 P22303 Acetylcholinesterase 87.83% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.02% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.76% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.05% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.87% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.03% 94.45%
CHEMBL1977 P11473 Vitamin D receptor 82.22% 99.43%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.19% 91.07%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.65% 97.36%
CHEMBL5028 O14672 ADAM10 81.53% 97.50%
CHEMBL237 P41145 Kappa opioid receptor 81.17% 98.10%
CHEMBL1937 Q92769 Histone deacetylase 2 80.57% 94.75%

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.
Andrographis paniculata

Cross-Links

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PubChem 11519131
NPASS NPC105518
LOTUS LTS0100731
wikiData Q105385230