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Assay Detail

CHEMBL3583702

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Functional
Cytotoxicity against human SKHEP1 cells assessed as inhibition of cell proliferation after 72 hrs by sulforhodamine B assay
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type SK-HEP1
Confidence 1 — Organism
Curated By Autocuration

Publication

Structure-Activity Relationships of Neplanocin A Analogues as S-Adenosylhomocysteine Hydrolase Inhibitors and Their Antiviral and Antitumor Activities.
Chandra G, Moon YW, Lee Y, Jang JY, Song J, Nayak A, Oh K, Mulamoottil VA, Sahu PK, Kim G, Chang TS, Noh M, Lee SK, Choi S, Jeong LS.
J Med Chem (2015) 58 : 5108 -5120
PubMed 26010585 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.32 6.14

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL154745 1 6.14
CHEMBL64718 FLUORO-NEPLANOCIN A 1 6.10
CHEMBL200935 DEAZANEPLANOCIN A 1 5.93
CHEMBL3580896 1 5.86
CHEMBL803 CYTARABINE 4.0 1 5.67
CHEMBL44657 ETOPOSIDE 4.0 1 5.55
CHEMBL8771 NEOPLANOCIN A 1 5.35
CHEMBL310547 1 5.21
CHEMBL3580900 1 5.09
CHEMBL80375 1 4.54
CHEMBL3580899 1 4.38
CHEMBL3580894 1 4.00
CHEMBL3580895 1 -
CHEMBL3580897 1 -
CHEMBL3580898 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL154745 IC50 = 720.0 nM 6.14
CHEMBL64718 FLUORO-NEPLANOCIN A IC50 = 800.0 nM 6.10
CHEMBL200935 DEAZANEPLANOCIN A IC50 = 1170.0 nM 5.93
CHEMBL3580896 IC50 = 1390.0 nM 5.86
CHEMBL803 CYTARABINE IC50 = 2120.0 nM 5.67
CHEMBL44657 ETOPOSIDE IC50 = 2800.0 nM 5.55
CHEMBL8771 NEOPLANOCIN A IC50 = 4500.0 nM 5.35
CHEMBL310547 IC50 = 6120.0 nM 5.21
CHEMBL3580900 IC50 = 8070.0 nM 5.09
CHEMBL80375 IC50 = 28890.0 nM 4.54
CHEMBL3580899 IC50 = 42090.0 nM 4.38
CHEMBL3580894 IC50 = 99180.0 nM 4.00
CHEMBL3580895 IC50 > 100000.0 nM -
CHEMBL3580897 IC50 > 100000.0 nM -
CHEMBL3580898 IC50 > 100000.0 nM -