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Compound Detail

CHEMBL488317

GINSENOSIDE R0
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CC1(C)CC[C@]2(C(=O)O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]6O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1

Basic Information

ChEMBL ID CHEMBL488317
Name GINSENOSIDE R0
Phase Preclinical
Structure Type MOL
InChI Key NFZYDZXHKFHPGA-QQHDHSITSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

957.1
MW (Da)
0.23
ALogP
18
HBA
11
HBD
312.1
PSA (Ų)
0.08
QED
3
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C48H76O19
MW 957.12
Aromatic Rings 0
Heavy Atoms 67
NP-Likeness 2.39

Activity Summary

IC50 1 meas. best 4.47

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.47 4.47 34000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 34000.0 nM 4.47 Inhibition of hyaluronidase (unknown origin) using hyaluronic acid as substrate ... 28202328

Literature References

PubMed DOI Target Context # Activities
2849641 10.1021/np50059a019 Unchecked 1
28202328 10.1016/j.bmcl.2017.01.083 Unchecked 1
28478866 10.1016/j.bmc.2017.04.023 Amyloid-beta precursor protein 1
33131725 10.1016/j.ejmech.2020.112932 AMP-activated protein kinase, AMPK 1
29353722 10.1016/j.ejmech.2018.01.011 Hepatocyte 1

Data from ChEMBL 36 via Core Engine