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THZ-531

CAS No.
1702809-17-3
Chemical Name:
THZ-531
Synonyms
THZ531;CPD1594;THZ-531;CS-2763;THZ531; THZ-531; THZ 531;THZ 531,inhibit,CDK,THZ-531,Cyclin dependent kinase,Inhibitor,THZ531;(R,E)-N-(4-(3-((5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl)amino)piperidine-1-carbonyl)phenyl)-4-(dimethylamino)but-2-enamide;(S,E)-N-(4-(3-((5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl)amino)piperidine-1-carbonyl)phenyl)-4-(dimethylamino)but-2-enamide;2-Butenamide, N-[4-[[(3R)-3-[[5-chloro-4-(1H-indol-3-yl)-2-pyrimidinyl]amino]-1-piperidinyl]carbonyl]phenyl]-4-(dimethylamino)-, (2E)-
CBNumber:
CB83153031
Molecular Formula:
C30H32ClN7O2
Molecular Weight:
558.07
MDL Number:
MFCD31563595
MOL File:
1702809-17-3.mol
Last updated:2023-09-04 15:51:00

THZ-531 Properties

Density 1.342±0.06 g/cm3(Predicted)
solubility ≥55.8 mg/mL in DMSO; insoluble in H2O; ≥4.9 mg/mL in EtOH
form solid
pka 13.12±0.70(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
NFPA 704
0
3 0

THZ-531 price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML2619 THZ531 ≥98% (HPLC) 1702809-17-3 5MG $102 2022-05-15 Buy
Sigma-Aldrich SML2619 THZ531 ≥98% (HPLC) 1702809-17-3 25MG $411 2022-05-15 Buy
Cayman Chemical 26386 THZ531 1702809-17-3 10mg $477 2024-03-01 Buy
Cayman Chemical 26386 THZ531 1702809-17-3 25mg $692 2024-03-01 Buy
Cayman Chemical 26386 THZ531 1702809-17-3 1mg $44 2024-03-01 Buy
Product number Packaging Price Buy
SML2619 5MG $102 Buy
SML2619 25MG $411 Buy
26386 10mg $477 Buy
26386 25mg $692 Buy
26386 1mg $44 Buy

THZ-531 Chemical Properties,Uses,Production

Uses

THZ 531 is a first-in-class CDK 12 and CDK13 covalent inhibitor. THZ531 causes a loss of gene expression with concurrent loss of elongating and hyperphosphorylated RNA polymerase II.

Definition

ChEBI: THZ531 is a member of the class of indoles that is 5-chloro-4-(1H-indol-3-yl)-N-[(3R)-piperidin-3-yl]pyrimidin-2-amine in which the piperidine NH group is substituted by a 4-{[(2E)-4-(dimethylamino)but-2-enoyl]amino}benzoyl group. It is a first-in-class CDK12 and CDK13 covalent kinase inhibitor with IC50 of 158 nM and 69 nM, respectively. It has a role as an apoptosis inducer, an antineoplastic agent and an EC 2.7.11.22 (cyclin-dependent kinase) inhibitor. It is a member of indoles, an organochlorine compound, a N-acylpiperidine, an aminopyrimidine, an enamide, a secondary carboxamide and a secondary amino compound.

Biological Activity

thz531 is a first-in-class cdk12 and cdk13 covalent inhibitor with ic50 values of 158 nm and 69 nm, respectively [1].complexes containing cdk12 and cdk13 regulate transcriptional elongation as well as processes, including mrna splicing and 3’-end rna processing. loss of cdk12 and cdk13, or of their cofactor cyclin k, impedes both pol ii processivity and rna processing [1].thz531 is an irreversible cdk12 and cdk13 covalent inhibitor. thz531 potently inhibited cdk12 and cdk13 with ic50 values of 158 nm and 69 nm, whereas inhibition of cdk7 and cdk9 was more than 50-fold weaker, with ic50s of 8.5 μm and 10.5 μm, respectively. in jurkat cells, thz531 irreversibly reduced cell proliferation with ic50 of 50 nm. thz531 induced apoptosis in a dose- and time-dependent way. thz531 also reduced pol ii c-terminal domain (ctd) ser2 phosphorylation, a mark of active transcriptional elongation, resulted in the loss of key super-enhancer-associated transcription factor genes and dna damage response (ddr) genes expression [1].1.zhang t, kwiatkowski n, olson cm, et al. covalent targeting of remote cysteine residues to develop cdk12 and cdk13 inhibitors. nat chem biol. 2016 oct;12(10):876-84.

THZ-531 Preparation Products And Raw materials

Raw materials

Preparation Products

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THZ531 THZ-531 CPD1594 (S,E)-N-(4-(3-((5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl)amino)piperidine-1-carbonyl)phenyl)-4-(dimethylamino)but-2-enamide (R,E)-N-(4-(3-((5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl)amino)piperidine-1-carbonyl)phenyl)-4-(dimethylamino)but-2-enamide CS-2763 THZ531; THZ-531; THZ 531 2-Butenamide, N-[4-[[(3R)-3-[[5-chloro-4-(1H-indol-3-yl)-2-pyrimidinyl]amino]-1-piperidinyl]carbonyl]phenyl]-4-(dimethylamino)-, (2E)- THZ 531,inhibit,CDK,THZ-531,Cyclin dependent kinase,Inhibitor,THZ531 1702809-17-3