2697112-33-5
2697112-33-5
Chemical Structure
JNJ-4355
Synonym(s): JNJ-78394355
- CAS No.: 2697112-33-5
- Formula:C40H43ClFN5O5S
- Molecular Weight:760.32
IUPAC Name: (Z)-15-chloro-96-fluoro-21-(2-(2-methoxyethoxy)ethyl)-13,23,61-trimethyl-11H,21H,61H-10-oxa-4-thia-1(4,1)-indola-2(4,5),6(3,5)-dipyrazola-9(3,1)-naphthalenacyclotridecaphane-12-carboxylic acid
InChIKey: LUVOYGUFQRWXGQ-UHFFFAOYSA-N
SMILES: CC1=C(C(O)=O)N(CCCOC2=CC3=CC4=C2C=CC(F)=C4)C5=CC=C(Cl)C(C6=C(CSCC7=NN(C)C(CC3)=C7)N(CCOCCOC)N=C6C)=C51
Biological Activity: JNJ-4355, a chemical probe, is a highly potent MCL-1 (myeloid cell leukemia-1) inhibitor, with KI of 18 pM. JNJ-4355 shows antitumor activity[1][2].
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JNJ-4355 | JNJ-4355, a chemical probe, is a highly potent MCL-1 (myeloid cell leukemia-1) inhibitor, with KI of 18 pM. JNJ-4355 shows antitumor activity. | |||||||||||||||||||||
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References
- [1]. Matthieu Jouffroy, et al. Synthesis of Atropisomeric Biaryls via Chiral Suzuki–Miyaura/Enzymatic Kinetic Resolution. ACS Catal. 2022, 12, 8380–8385.
- [2]. Frederik J. Rombouts, et al. Abstract 2133: In pursuit of MCL-1 inhibitors with improved therapeutic window for the treatment of hematological malignancies: Discovery of JNJ-4355. Cancer Res (2022) 82 (12_Supplement): 2133.
