1. Metabolic Enzyme/Protease
  2. Endogenous Metabolite
  3. Stephacidin B

Stephacidin B is a fungal metabolite. Stephacidin B shows in vitro cytotoxicity against a panel of human tumor cell lines. Stephacidin B shows the strongest cytotoxicity against testosterone-dependent prostate LNCaP cancer cells.

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

Stephacidin B Chemical Structure

Stephacidin B Chemical Structure

CAS No. : 360765-75-9

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Based on 1 publication(s) in Google Scholar

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Description

Stephacidin B is a fungal metabolite. Stephacidin B shows in vitro cytotoxicity against a panel of human tumor cell lines. Stephacidin B shows the strongest cytotoxicity against testosterone-dependent prostate LNCaP cancer cells[1].

IC50 & Target[1]

Microbial Metabolite

 

Molecular Weight

891.02

Formula

C52H54N6O8

CAS No.
SMILES

O=C1N(CCC2)[C@]23C[C@]4([H])[C@@]1(N5C3=O)[C@]([H])(C67C8=C(C(C=CC(C)(C)O9)=C9C=C8)[N+]([O-])=C6C(C)(C)[C@@]%10([H])[C@@](C(N%11CCCC%11%12C%10)=O)(NC%12=O)[C@@]75[H])C%13=C(N(C%14=C%15C(OC(C)(C)C=C%15)=CC=C%14%13)O)C4(C)C

Structure Classification
Initial Source

Aspergillus ochraceus

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

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

Purity & Documentation
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    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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Stephacidin B
Cat. No.:
HY-N10265
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