Ichangic acid 17-beta-D-glucopyranoside

Details

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Internal ID dfbec61e-7f22-48d1-bf52-181a1039a6e3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name
SMILES (Canonical) CC1(CCC2C(C13C(O3)C(=O)O)(C(=O)CC(C24COC(=O)CC4O)C(C)(C)O)C)C(C5=COC=C5)OC6C(C(C(C(O6)CO)O)O)O
SMILES (Isomeric) CC1(CCC2C(C13C(O3)C(=O)O)(C(=O)CC(C24COC(=O)CC4O)C(C)(C)O)C)C(C5=COC=C5)OC6C(C(C(C(O6)CO)O)O)O
InChI InChI=1S/C32H44O15/c1-28(2,42)17-9-18(34)30(4)16(31(17)13-44-20(36)10-19(31)35)5-7-29(3,32(30)25(47-32)26(40)41)24(14-6-8-43-12-14)46-27-23(39)22(38)21(37)15(11-33)45-27/h6,8,12,15-17,19,21-25,27,33,35,37-39,42H,5,7,9-11,13H2,1-4H3,(H,40,41)
InChI Key ZOJPKDNYMBAQJP-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C32H44O15
Molecular Weight 668.70 g/mol
Exact Mass 668.26802069 g/mol
Topological Polar Surface Area (TPSA) 246.00 Ų
XlogP -1.60
Atomic LogP (AlogP) -0.56
H-Bond Acceptor 14
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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Ichangic acid 17-b-D-glucopyranoside
Ichangic acid 17-beta-D-glucopyranoside

2D Structure

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2D Structure of Ichangic acid 17-beta-D-glucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6914 69.14%
Caco-2 - 0.8705 87.05%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7634 76.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8179 81.79%
OATP1B3 inhibitior + 0.9187 91.87%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior + 0.6792 67.92%
P-glycoprotein substrate + 0.6326 63.26%
CYP3A4 substrate + 0.7099 70.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.5306 53.06%
CYP2C9 inhibition - 0.7883 78.83%
CYP2C19 inhibition - 0.8322 83.22%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.8816 88.16%
CYP2C8 inhibition + 0.6553 65.53%
CYP inhibitory promiscuity - 0.9562 95.62%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6033 60.33%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9061 90.61%
Skin irritation - 0.7029 70.29%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis - 0.6969 69.69%
Human Ether-a-go-go-Related Gene inhibition + 0.7842 78.42%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9110 91.10%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7628 76.28%
Acute Oral Toxicity (c) I 0.5640 56.40%
Estrogen receptor binding + 0.7462 74.62%
Androgen receptor binding + 0.7841 78.41%
Thyroid receptor binding - 0.5218 52.18%
Glucocorticoid receptor binding + 0.7217 72.17%
Aromatase binding + 0.6906 69.06%
PPAR gamma + 0.7168 71.68%
Honey bee toxicity - 0.7143 71.43%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9577 95.77%

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
CHEMBL2581 P07339 Cathepsin D 97.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.61% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.96% 85.14%
CHEMBL220 P22303 Acetylcholinesterase 95.29% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.11% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.72% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 91.98% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.39% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.23% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.33% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.23% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.19% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.16% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.85% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.25% 99.23%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 85.57% 94.23%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 85.36% 100.00%
CHEMBL5028 O14672 ADAM10 84.81% 97.50%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.64% 95.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.76% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.65% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.17% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.58% 92.62%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.27% 93.04%

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.
Citrus × aurantium

Cross-Links

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PubChem 72995477
LOTUS LTS0213918
wikiData Q105380532