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Compound Detail

CHEMBL409627

CONFERTIFLORIN
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C=C1C(=O)O[C@@H]2[C@H]1[C@@H](OC(C)=O)C[C@H](C)[C@@H]1CCC(=O)[C@@]21C

Basic Information

ChEMBL ID CHEMBL409627
Name CONFERTIFLORIN
Phase Preclinical
Structure Type MOL
InChI Key VWBKXLDATRBPOE-VICSMPQUSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

306.4
MW (Da)
2.04
ALogP
5
HBA
0
HBD
69.7
PSA (Ų)
0.55
QED
0
Ro5 Violations
1
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C17H22O5
MW 306.36
Aromatic Rings 0
Heavy Atoms 22
NP-Likeness 3.32

Activity Summary

IC50 2 meas. best 5.54

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Prostaglandin G/H synthase 2
CHEMBL230
IC50 5.54 5.54 2900.0 1
Platelet
CHEMBL4296519
IC50 5.05 5.05 8880.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Prostaglandin G/H synthase 2 IC50 = 2900.0 nM 5.54 Inhibition of COX2 16038536
Platelet IC50 = 8880.0 nM 5.05 Inhibition of serotonin release in bovine platelets 18271521

Literature References

PubMed DOI Target Context # Activities
18271521 10.1021/jm701318x Platelet 1
16038536 10.1021/np049655u Prostaglandin G/H synthase 2 1

Data from ChEMBL 36 via Core Engine