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Assay Detail

CHEMBL5111592

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of CDK6/Cyclin-D3 (unknown origin)
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 7 — Homologous single protein target
Curated By Autocuration

Target

CDK6/cyclin D3 (CHEMBL2111448)
Type PROTEIN COMPLEX
Organism Homo sapiens

Publication

Potent GCN2 Inhibitor Capable of Reversing MDSC-Driven T Cell Suppression Demonstrates In Vivo Efficacy as a Single Agent and in Combination with Anti-Angiogenesis Therapy.
Jackson JJ, Shibuya GM, Ravishankar B, Adusumilli L, Bradford D, Brockstedt DG, Bucher C, Bui M, Cho C, Colas C, Cutler G, Dukes A, Han X, Hu DX, Jacobson S, Kassner PD, Katibah GE, Ko MYM, Kolhatkar U, Leger PR, Ma A, Marshall L, Maung J, Ng AA, Okano A, Pookot D, Poon D, Ramana C, Reilly MK, Robles O, Schwarz JB, Shakhmin AA, Shunatona HP, Sreenivasan R, Tivitmahaisoon P, Xu M, Zaw T, Wustrow DJ, Zibinsky M.
J Med Chem (2022) 65 : 12895 -12924
PubMed 36127295 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.72 6.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5190023 1 6.72

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5190023 IC50 = 191.0 nM 6.72