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Compound Detail

CHEMBL303403

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CC[C@@H]1/C=C(\C)C[C@H](C)C[C@H](OC)[C@H]2O[C@@](O)(C(=O)C(=O)N3CCCC[C@H]3C(=O)O[C@H](/C(C)=C/[C@@H]3CC[C@H](NCCOCc4ccccc4)[C@H](OC)C3)[C@H](C)CCC1=O)[C@H](C)C[C@@H]2OC

Basic Information

ChEMBL ID CHEMBL303403
Phase Preclinical
Structure Type MOL
InChI Key GOUFWHWWDVMNIR-PVIJIYLYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

909.2
MW (Da)
7.32
ALogP
12
HBA
2
HBD
159.2
PSA (Ų)
0.09
QED
3
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C52H80N2O11
MW 909.21
Aromatic Rings 1
Heavy Atoms 65
NP-Likeness 0.98

Activity Summary

IC50 1 meas. best 7.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
T-cell
CHEMBL614309
IC50 7.89 7.89 13.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
T-cell IC50 = 13.0 nM 7.89 In vitro suppression of T-cell proliferation. -

Literature References

PubMed DOI Target Context # Activities
- 10.1016/S0960-894X(97)00409-5 T-cell 1

Data from ChEMBL 36 via Core Engine