Skip to main content

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

Cyclin-dependent Kinase Inhibitors: Small Molecules and Peptides

What are Cyclins?

Cyclins are a heterogeneous family of proteins that have a common 100 amino acid sequence called the cyclin box. Their only cellular role is to activate CDKs, and their expression fluctuates throughout the cell cycle, dependent on the cell cycle phase they are involved in. There are several subfamilies of cyclins, and several 'orphan' cyclins for which no CDK binding partner has been identified.

CDK Structure & Localization

CDKs are constitutively expressed and range in size ...

Show More

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

Cdk1 inhibitor

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

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 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

Cdk8 inhibitor

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

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

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

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

Potent and selective ATP-competitive CDK9 inhibitor

Chemical Name: 4-[[[5'-Chloro-2'-[[trans-4-[[(1R)-2-methoxy-1-methylethyl]amino]cyclohexyl]amino][2,4'-bipyridin]-6-yl]amino]methyl]tetrahydro-2H-pyran-4-carbonitrile
Purity: ≥97% (HPLC)
Potent and selective ATP-competitive CDK9 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

Potent and selective cdk inhibitor; orally bioavailable

Chemical Name: [4-Amino-2-[[1-(methylsulfonyl)-4-piperidinyl]amino]-5-pyrimidinyl](2,3-difluoro-6-methoxyphenyl)methanone
Purity: ≥98% (HPLC)
Potent and selective cdk inhibitor; orally bioavailable

Potent cdk inhibitor

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

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

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

SETD8 inhibitor; also CDK4 inhibitor

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

Cdk inhibitor; potently inhibits cdk9; also inhibits MK2

Chemical Name: 1,5,6,7-Tetrahydro-2-(4-pyridinyl)-4H-pyrrolo[3,2-c]pyridin-4-one hydrochloride
Purity: ≥98% (HPLC)
Cdk inhibitor; potently inhibits cdk9; also inhibits MK2

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

Cdk inhibitor; potently inhibits cdk1, cdk2 and cdk5

Alternate Names: NG 60
Chemical Name: (2R)-2-[[6-[(3-Chlorophenyl)amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]-3-methyl-1-butanol
Purity: ≥98% (HPLC)
Cdk inhibitor; potently inhibits cdk1, cdk2 and cdk5

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

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

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 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

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

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
Results Per Page
5 10 25 50
/ 2