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Proteins and peptidesOur latest ELISA kit: Human Tau (phospho T217) - Intracellular
Highly sensitive kit offering the most promising biomarkers for Alzheimer’s disease diagnostics. Learn about all product ranges with our product overviews.
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MW 293.28 Da, Purity >96%. Potent CDK inhibitor (IC50 values are 3.5 (CDK1/cyclin B), 20 (CDK2/cyclin A) and 40 nM (CDK5/p35)). Also displays potent and selective inhibition of GSK-3β (IC50 values are 40 and 4 nM respectively). Antiproliferative effects seen in vitro. Cell-permeable.
Alternative names=AI838772, AW493413, CCNB, CCNB1_HUMAN, CCNB2_HUMAN, CD5R1_HUMAN, CDC28, CDC28A, CDC2A, CDK1_HUMAN, CDK2_HUMAN, CDK5 activator 1, CDK5P35, CDK5R, CDK5R1, CDK5_HUMAN, CDKN1, CDKN2, CELL CYCLE CONTROLLER CDC2, Cdc 2, Cell Divsion Cycle 2 Protein, Cell devision kinase 2, Cell division control protein 2, Cell division control protein 2 homolog, Cell division cycle 2 G1 to S and G2 to M, Cell division protein kinase 1, Cell division protein kinase 2, Cell division protein kinase 5, Crk6, CycB2, Cyclin B1, Cyclin B2, Cyclin-dependent kinase 1, Cyclin-dependent kinase 2, Cyclin-dependent kinase 5, Cyclin-dependent kinase 5 activator 1, Cyclin-dependent kinase 5 regulatory subunit 1, DKFZP586N0721, DKFZp686D0638, DKFZp686J10186, DKFZp686L20222, FLJ11090, G2 mitotic specific cyclin B1, G2 mitotic specific cyclin B2, G2/mitotic specific cyclin B3, G2/mitotic-specific cyclin-B1, G2/mitotic-specific cyclin-B2, GSK-3 alpha, GSK-3 beta, GSK3A_HUMAN, GSK3B_HUMAN, GSK3beta isoform, Glycogen synthase kinase-3 alpha, Glycogen synthase kinase-3 beta, HSPC193, HST17436, HsT17299, JV15-2, LDS1C, LDS3, MAD (mothers against decapentaplegic Drosophila) homolog 3, MAD homolog 3, MAD, mothers against decapentaplegic homolog 3, MADH 3, MGC104252, MGC108931, MGC111195, MGC112732, MGC140694, MGC60396, MPF, Mad homolog JV15 2, Mad protein homolog, Mothers against DPP homolog 3, Mothers against decapentaplegic homolog 3, NCK 5A, Neuronal CDK5 activator, P23, P34CDC2, P35, PSSALRE, Protein kinase CDK5 splicing, RP11 805H4.3, RP24-311F12.2, Regulatory partner for CDK5 kinase, SCAN1, SMA and MAD related protein 3, SMAD, SMAD family member 3, SMAD, mothers against DPP homolog 3, SMAD3_HUMAN, Serine threonine protein kinase PSSALRE, Serine/threonine protein kinase GSK3A, Serine/threonine-protein kinase GSK3B, Serine/threonine-protein kinase PSSALRE, TPKII catalytic subunit, TPKII regulatory subunit, TYDP, TYDP1_HUMAN, Tau protein kinase II 23 kDa subunit, Tau protein kinase II catalytic subunit, Tyr-DNA phosphodiesterase 1, Tyrosyl-DNA phosphodiesterase 1, cdc2-related protein kinase, cyclin dependent kinase 2-alpha, hMAD-3, hSMAD3, kinase Cdc2, p25, p33 protein kinase, p33(CDK2), p34 Cdk1, p34 protein kinase
237430-03-4
> 96%
Solid
293.28 Da
C16H11N3O3
5005498
Synthetic
MW 293.28 Da, Purity >96%. Potent CDK inhibitor (IC50 values are 3.5 (CDK1/cyclin B), 20 (CDK2/cyclin A) and 40 nM (CDK5/p35)). Also displays potent and selective inhibition of GSK-3β (IC50 values are 40 and 4 nM respectively). Antiproliferative effects seen in vitro. Cell-permeable.
Alternative names=AI838772, AW493413, CCNB, CCNB1_HUMAN, CCNB2_HUMAN, CD5R1_HUMAN, CDC28, CDC28A, CDC2A, CDK1_HUMAN, CDK2_HUMAN, CDK5 activator 1, CDK5P35, CDK5R, CDK5R1, CDK5_HUMAN, CDKN1, CDKN2, CELL CYCLE CONTROLLER CDC2, Cdc 2, Cell Divsion Cycle 2 Protein, Cell devision kinase 2, Cell division control protein 2, Cell division control protein 2 homolog, Cell division cycle 2 G1 to S and G2 to M, Cell division protein kinase 1, Cell division protein kinase 2, Cell division protein kinase 5, Crk6, CycB2, Cyclin B1, Cyclin B2, Cyclin-dependent kinase 1, Cyclin-dependent kinase 2, Cyclin-dependent kinase 5, Cyclin-dependent kinase 5 activator 1, Cyclin-dependent kinase 5 regulatory subunit 1, DKFZP586N0721, DKFZp686D0638, DKFZp686J10186, DKFZp686L20222, FLJ11090, G2 mitotic specific cyclin B1, G2 mitotic specific cyclin B2, G2/mitotic specific cyclin B3, G2/mitotic-specific cyclin-B1, G2/mitotic-specific cyclin-B2, GSK-3 alpha, GSK-3 beta, GSK3A_HUMAN, GSK3B_HUMAN, GSK3beta isoform, Glycogen synthase kinase-3 alpha, Glycogen synthase kinase-3 beta, HSPC193, HST17436, HsT17299, JV15-2, LDS1C, LDS3, MAD (mothers against decapentaplegic Drosophila) homolog 3, MAD homolog 3, MAD, mothers against decapentaplegic homolog 3, MADH 3, MGC104252, MGC108931, MGC111195, MGC112732, MGC140694, MGC60396, MPF, Mad homolog JV15 2, Mad protein homolog, Mothers against DPP homolog 3, Mothers against decapentaplegic homolog 3, NCK 5A, Neuronal CDK5 activator, P23, P34CDC2, P35, PSSALRE, Protein kinase CDK5 splicing, RP11 805H4.3, RP24-311F12.2, Regulatory partner for CDK5 kinase, SCAN1, SMA and MAD related protein 3, SMAD, SMAD family member 3, SMAD, mothers against DPP homolog 3, SMAD3_HUMAN, Serine threonine protein kinase PSSALRE, Serine/threonine protein kinase GSK3A, Serine/threonine-protein kinase GSK3B, Serine/threonine-protein kinase PSSALRE, TPKII catalytic subunit, TPKII regulatory subunit, TYDP, TYDP1_HUMAN, Tau protein kinase II 23 kDa subunit, Tau protein kinase II catalytic subunit, Tyr-DNA phosphodiesterase 1, Tyrosyl-DNA phosphodiesterase 1, cdc2-related protein kinase, cyclin dependent kinase 2-alpha, hMAD-3, hSMAD3, kinase Cdc2, p25, p33 protein kinase, p33(CDK2), p34 Cdk1, p34 protein kinase
237430-03-4
> 96%
Solid
293.28 Da
C16H11N3O3
5005498
Synthetic
Alsterpaullone
Potent CDK inhibitor (IC50 values are 3.5 (CDK1/cyclin B), 20 (CDK2/cyclin A) and 40 nM (CDK5/p35)). Also displays potent and selective inhibition of GSK-3β (IC50 values are 40 and 4 nM respectively). Antiproliferative effects seen in vitro. Cell-permeable.
C1C2=C(C3=CC=CC=C3NC1=O)NC4=C2C=C(C=C4)[N+](=O)[O-]
InChI=1S/C16H11N3O3/c20-15-8-12-11-7-9(19(21)22)5-6-14(11)18-16(12)10-3-1-2-4-13(10)17-15/h1-7,18H,8H2,(H,17,20)
OLUKILHGKRVDCT-UHFFFAOYSA-N
9-nitro-7,12-dihydro-5H-indolo[3,2-d][1]benzazepin-6-one
Ambient - Can Ship with Ice
+4°C
Store under desiccating conditions, The product can be stored for up to 12 months
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