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Merck
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重要文件

SML1719

Sigma-Aldrich

BPC 157 trifluoroacetate salt

≥95% (HPLC)

同義詞:

BPC-157, Booly Protection Compound 15, GEPPPGKPADDAGLV, Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val

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About This Item

經驗公式(希爾表示法):
C62H98N16O22 · xC2HF3O2
CAS號碼:
分子量::
1419.54 (free base basis)
分類程式碼代碼:
12352200
NACRES:
NA.77

品質等級

化驗

≥95% (HPLC)

形狀

film

顏色

colorless

運輸包裝

wet ice

儲存溫度

−20°C

SMILES 字串

N2([C@@H](CCC2)C(=O)N3[C@@H](CCC3)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N4[C@@H](CCC4)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)O)C(=O)[C@H]1N(CCC1)C(=O)[C@@H](NC(=O)CN)CCC(=O)O

InChI 密鑰

HEEWEZGQMLZMFE-RKGINYAYSA-N

生化/生理作用

BPC 157 is a gut peptide and possesses free radical scavenging activity. This peptide stimulates nitric oxide synthase generation and therefore offers gastric cytoprotection. Unlike other peptides, BPC 157 is effective without a carrier. It participates in muscle healing and is used in the treatment of gastrocnemius muscle complex.
BPC 157 is a stable gastric pentadecapeptide that exhibit anti-ulcer and wounds/fistulas healing properties.
BPC 157 is a stable gastric pentadecapeptide that exhibit anti-ulcer and wounds/fistulas healing properties. BPC 157 reduces immediate and delayed damage induced brain trauma and improves nerve regeneration after transection. BPC 157 displays antianxiety and antidepressant effects. It appears that BPC 157 promotes proliferation, migration, and tube formation of human umbilical vein endothelial cells through activation of ERK1/2 phosphorylation.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析證明 (COA)

Lot/Batch Number

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Gastric pentadecapeptide BPC 157 as an effective therapy for muscle crush injury in the rat.
Novinscak T, et al.
Surgery Today, 38(8), 716-725 (2008)
The influence of a novel pentadecapeptide, BPC 157, on NG-nitro-L-arginine methylester and L-arginine effects on stomach mucosa integrity and blood pressure.
Sikiric P, et al.
European Journal of Pharmacology, 332(1), 23-33 (1997)

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