Phyto4Health

20-Hydroxyecdysone

Representations & DB's id

ChEBI: CHEBI:16587
ChEMBL: CHEMBL224128
PubChem: 5459840
IUPAC: (2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
Standard InChI: InChI=1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15-,17-,19+,20-,21-,22+,24+,25+,26+,27+/m0/s1
Standard InChI Key: NKDFYOWSKOHCCO-YPVLXUMRSA-N
SMILES: O[C@H]1C[C@@]2(C)[C@@H](C[C@H]1O)C(=O)C=C1[C@@H]2CC[C@]2([C@@]1(O)CC[C@@H]2[C@]([C@@H](CCC(O)(C)C)O)(O)C)C

Molecular propeties

AlogP: 1.85
Hydrogen bonds acceptors: 7
Hydrogen bonds donors: 6
Rotatable bonds: 5
Number of rings: 4
Molecular Weight: 480.31
Topological polar surface area: 138
Number of aromatic rings: 0
Fsp3: 0.889
Number of carbons: 27

Plant sources

Part of plant Plant name Ref.
PlantVinca minor
PlantVinca minor

In vitro data

Activity Type Activity Value Target Name UniProt ID Ref.
Potency17782.8 nMEyes absent homolog 2O00167
Others1.76 P-glycoprotein 1P08183
Potency1412.5 nMGemininO75496
Others71.2 %ButyrylcholinesteraseP06276
IC50506 ug/mlButyrylcholinesteraseP06276