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14 results for "CDC2/CDK1 Small Molecules and Peptides" in Products

CDC2/CDK1: Small Molecules and Peptides

CDC2 (Cell Division Cycle 2), also known as CDK1 (Cyclin Dependent Kinase 1), is a member of the CDK family of serine/threonine kinases. The CDKs are important regulators of cell cycle progression and their activities are largely controlled by association with Cyclins, and activating and inhibitory phosphorylations. Entry into mitosis is initiated by CDC2. Full activation of CDC2 requires phosphorylation at T161 and association with CyclinB. In contrast, phosphorylation of CDC2 at Y15 and T14 during the G2-phase of the cell cycle inhibits activity, and dephosphorylation of Y15 and T14 by CDC25 phosphatase during late G2 restores activity.

Cdk1 inhibitor

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

α1 and α2B antagonist; also MT3 antagonist

Chemical Name: 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-furanylcarbonyl)piperazine hydrochloride
Purity: ≥98% (HPLC)
α1 and α2B antagonist; also MT3 antagonist

Potent CDK1 inhibitor

Chemical Name: rel-N2-[(1R,2S)-2-Aminocyclohexyl]-N6-(3-chlorophenyl)-9-ethyl-9H-purine-2,6-diamine dihydrochloride
Purity: ≥98% (HPLC)
Potent CDK1 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 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

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

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

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 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

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 cdk inhibitor

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