1. Epigenetics Cell Cycle/DNA Damage MAPK/ERK Pathway Stem Cell/Wnt TGF-beta/Smad Cytoskeleton
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  3. 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine

3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine 

Cat. No.: HY-N12466
Handling Instructions

3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine (Compound 7) is an inhibitor of protein kinases, with IC50s of 0.092, 0.26, 0.77 μM for PKC-α, ROCK, ASK1. 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine shows potent cytotoxicity against PC-3 cancer cells with an IC50 value of 0.16 μM.

For research use only. We do not sell to patients.

3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine Chemical Structure

3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine Chemical Structure

CAS No. : 2226941-29-1

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Description

3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine (Compound 7) is an inhibitor of protein kinases, with IC50s of 0.092, 0.26, 0.77 μM for PKC-α, ROCK, ASK1. 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine shows potent cytotoxicity against PC-3 cancer cells with an IC50 value of 0.16 μM[1].

Molecular Weight

480.51

Formula

C28H24N4O4

CAS No.
SMILES

O=C1C2=C3C(N4C5=C3C=CC=C5)=C6C(C(C=CC=C7)=C7N6[C@]8(C)[C@H](O)[C@@H](NC(C)=O)C[C@@]4([H])O8)=C2CN1

Structure Classification
Initial Source

Streptomyces sp

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine
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HY-N12466
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