Staurosporine – A protein kinase inhibitor

Staurosporine – A protein kinase inhibitor

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Catalog# 1048

Size: 1 mg

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Potent inhibitor of protein kinase C and most other kinases, including tyrosine kinases. Inhibits topoisomerase II directly by blocking transfer of phosphodiester bonds from DNA to active site tyrosine. Induces apoptosis in CHO cells at 1 µM.


Cat # +Size 1048-01 (Size: 100 µg)
1048-1 (Size: 1 mg)
Alternate NameAntibiotic AM-2282
Appearance Pale yellow solid
CAS # 62996-74-1
Molecular Formula C₂₈H₂₆N₄O₃
Molecular Weight 466.53
Purity>99% by TLC
SolubilityDMSO ( 25 mg/ml)
InChi InChI=1S/C28H26N4O3/c1-28-26(34-3)17(29-2)12-20(35-28)31-18-10-6-4-8-14(18)22-23-16(13-30-27(23)33)21-15-9-5-7-11-19(15)32(28)25(21)24(22)31/h4-11,17,20,26,29H,12-13H2,1-3H3,(H,30,33)/t17-,20-,26-,28+/m0/s1
InChi Key
PubChem CID 451705
MDL NumberMFCD00077402
Handling Protect from light and moisture
Storage Conditions4°C
Shipping ConditionsRT
USAGE For Research Use Only! Not For Use in Humans.




Ellen Brenner, Cancer immune control needs senescence induction by interferon-dependent cell cycle regulator pathways in tumours. Nat Commun., Mar. 2020; 32165639.

Carles Solà-Riera, Orthohantaviruses belonging to three phylogroups all inhibit apoptosis in infected target cells. Sci Rep., Jan. 2019; 30696898.

Debnath et al., Hsp90 Inhibitors as New Leads To Target Parasitic Diarrheal Diseases. Antimicrob. Agents Chemother., Jul 2014; 58: 4138 - 4144.

Lin K-R et al. (2007) J. Biol. Chem. 282: 21962-21972.

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