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Cyclin-dependent Kinase Inhibitors: Small Molecules and Peptides

35 results for "Cyclin-dependent Kinase Inhibitors Small Molecules and Peptides" in Products

35 results for "Cyclin-dependent Kinase Inhibitors Small Molecules and Peptides" in Products

Cyclin-dependent Kinase Inhibitors: Small Molecules and Peptides

Potent cdk4 and cdk6 inhibitor; brain penetrant

Alternate Names: Palbociclib
Chemical Name: 6-acetyl-8-cyclopentyl-5-methyl-2-[[5-(1-piperazinyl)-2-pyridinyl]amino]pyrido[2,3-d]pyrimidin-7(8H)-one isethionate salt
Purity: ≥98% (HPLC)
Potent cdk4 and cdk6 inhibitor; brain penetrant

Dual cdk4/cdk6 inhibitor; orally bioavailable

Alternate Names: LEE-011
Chemical Name: 7-Cyclopentyl-N,N-dimethyl-2-[[5-(1-piperazinyl)-2-pyridinyl]amino]-7H-pyrrolo[2,3-d]pyrimidine-6-carboxamide
Purity: ≥98% (HPLC)
Dual cdk4/cdk6 inhibitor; orally bioavailable

Cdk inhibitor; potently inhibits cdk2 and cdk9

Alternate Names: L 86-8275
Chemical Name: 2-(2-Chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidinyl]-4H-1-benzopyran-4-one hydrochloride
Purity: ≥98% (HPLC)
Cdk inhibitor; potently inhibits cdk2 and cdk9

Potent CK1 inhibitor; also inhibits cyclin-dependent kinases

Chemical Name: 2-[[9-(1-Methylethyl)-6-[[3-(2-pyridinyl)phenyl]amino]-9H-purin-2-yl]amino]-1-butanol dihydrochloride
Purity: ≥98% (HPLC)
Potent CK1 inhibitor; also inhibits cyclin-dependent kinases

Potent and selective B-Raf, CDK16 and NEK9 inhibitor; anticancer; also targets human proteins in the SARS-CoV-2 interactome

Chemical Name: N-[3-[5-(2-Aminopyrimidin-4-yl)-2-tert-butyl-1,3-thiazol-4-yl]-2-fluorophenyl]-2,6-difluorobenzenesulfonamide methanesulfonate
Purity: ≥98% (HPLC)
Potent and selective B-Raf, CDK16 and NEK9 inhibitor; anticancer; also targets human proteins in the SARS-CoV-2 interactome

Potent and selective inhibitor of CDK2, CDK5, CDK1 and CDK9

Alternate Names: SCH 727965
Chemical Name: (2S)-1-[3-Ethyl-7-[[(1-oxido-3-pyridinyl)methyl]amino]pyrazolo[1,5-a]pyrimidin-5-yl]-2-piperidineethanol
Purity: ≥98% (HPLC)
Potent and selective inhibitor of CDK2, CDK5, CDK1 and CDK9

Cdk1 inhibitor

Chemical Name: 5-(6-Quinolinylmethylene)-2-[(2-thienylmethyl)amino]-4(5H)-thiazolone
Purity: ≥98% (HPLC)
Cdk1 inhibitor

Potent and selective CDK7 inhibitor; induces cell cycle arrest

Chemical Name: N-[(1S)-2-(Dimethylamino)-1-phenylethyl]-4,6-dihydro-6,6-dimethyl-3-[[4-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]pyrrolo[3,4-c]pyrazole-5(1H)-carboxamide
Purity: ≥95% (HPLC)
Potent and selective CDK7 inhibitor; induces cell cycle arrest

Selective cdk7 inhibitor

Chemical Name: N5-(6-Aminohexyl)-3-(1-methylethyl)-N7-(phenylmethyl)pyrazolo[1,5-a]pyrimidine-5,7-diamine dihydrochloride
Purity: ≥98% (HPLC)
Selective cdk7 inhibitor

Potent CDK14 and CDK16 inhibitor; displays reversible inhibition of CDK14

Chemical Name: N-(1-((3-(4-(Dimethylamino)butanamido)phenyl)sulfonyl)piperidin-4-yl)-4-(2,4,6-trichlorobenzamido)-1H-pyrazole-3-carboxamide
Purity: ≥98% (HPLC)
Potent CDK14 and CDK16 inhibitor; displays reversible inhibition of CDK14

GSK-3β inhibitor; also inhibits cdks

Chemical Name: 9-Bromo-7,12-dihydro-indolo[3,2-d][1]benzazepin-6(5H)-one
Purity: ≥98% (HPLC)
GSK-3β inhibitor; also inhibits cdks

Potent and selective CDK8 and CDK19 inhibitor; maintains pluripotency of mouse PSCs in culture

Chemical Name: N-Propyl-3-(4-pyridinyl)imidazo[1,2-b]pyridazin-6-amine
Purity: ≥98% (HPLC)
Potent and selective CDK8 and CDK19 inhibitor; maintains pluripotency of mouse PSCs in culture

Potent covalent CDK14 and CDK16 inhibitor; also inhibits other TAIRE kinase family members

Chemical Name: N-[1-[[3-[[(2E)-4-(Dimethylamino)-1-oxo-2-buten-1-yl]amino]phenyl]sulfonyl]-4-piperidinyl]-4-[(2,4,6- trichlorobenzoyl)amino]-1H-pyrazole-3-carboxamide
Purity: ≥98% (HPLC)
Potent covalent CDK14 and CDK16 inhibitor; also inhibits other TAIRE kinase family members

SKP2 (S-phase kinase-associated protein 2) inhibitor; upregulates p27 and arrests cell cycle in G1 phase

Chemical Name: N-(4-Butyl-2-methylphenyl)acetamide
Purity: ≥98% (HPLC)
SKP2 (S-phase kinase-associated protein 2) inhibitor; upregulates p27 and arrests cell cycle in G1 phase

Cdk inhibitor

Alternate Names: CYC 202,Seliciclib
Chemical Name: (2R)-2-[[9-(1-Methylethyl)-6-[(phenylmethyl)amino]-9H-purin-2-yl]amino]-1-butanol
Purity: ≥98% (HPLC)
Cdk inhibitor

Cdk2 and cdk5 inhibitor

Chemical Name: 2,2'-[[6-[[(4-Methoxyphenyl)methyl]amino]-9-(1-methylethyl)-9H-purin-2-yl]imino]bis[ethanol]
Purity: ≥98% (HPLC)
Cdk2 and cdk5 inhibitor

Cdk inhibitor; potently inhibits cdk1, 2, 5 and 9

Chemical Name: 4-[2-Methyl-1-(1-methylethyl)-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-2-pyrimidinamine
Purity: ≥98% (HPLC)
Cdk inhibitor; potently inhibits cdk1, 2, 5 and 9

Potent and selective PKMYT1 inhibitor

Alternate Names: Lunresertib
Chemical Name: (S)-2-Amino-1-(3-hydroxy-2,6-dimethylphenyl)-5,6-dimethylpyrrolo[2,3-b]pyridine-3-carboxamide
Purity: ≥98% (HPLC)
Potent and selective PKMYT1 inhibitor

Cdk8 inhibitor

Chemical Name: 4-[(2-Phenylethyl)amino]-6-quinazolinecarbonitrile hydrochloride
Purity: ≥98% (HPLC)
Cdk8 inhibitor

Selective cdk inhibitor; potently inhibits cdk1, cdk2 and cdk5

Alternate Names: NG 95
Chemical Name: (2R)-2-[[6-[(3-Chloro-4-carboxyphenyl)amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]-3-methyl-1-butanol
Purity: ≥98% (HPLC)
Selective cdk inhibitor; potently inhibits cdk1, cdk2 and cdk5

Cdk inhibitor; potently inhibits cdk2, cdk7 and cdk9

Alternate Names: BMS-387032
Chemical Name: N-[5-[[[5-(1,1-Dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4-piperidinecarboxamide
Purity: ≥98% (HPLC)
Cdk inhibitor; potently inhibits cdk2, cdk7 and cdk9

Potent cdk inhibitor

Chemical Name: 3-[[4-[2-[(3-Chlorophenyl)amino]-4-pyrimidinyl]-2-pyridinyl]amino]-1-propanol
Purity: ≥98% (HPLC)
Potent cdk inhibitor

Potent CDK2 inhibitor

Alternate Names: AUZ 454
Chemical Name: N-[4-[(2-Amino-4-pyrimidinyl)oxy]phenyl]-N'-[4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl]urea
Purity: ≥98% (HPLC)
Potent CDK2 inhibitor

Cdk inhibitor; potently inhibits cdk1 and cdk2

Chemical Name: (4-Butoxy-1H-pyrazolo[3,4-b]pyridin-5-yl) (2,6-difluoro-4-methylphenyl)methanone
Purity: ≥97% (HPLC)
Cdk inhibitor; potently inhibits cdk1 and cdk2

SETD8 inhibitor; also CDK4 inhibitor

Chemical Name: 2-Methyl-5-[(4-methylphenyl)amino]-4,7-benzothiazoledione
Purity: ≥98% (HPLC)
SETD8 inhibitor; also CDK4 inhibitor
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