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197250-15-0

中文名稱 GAP26
英文名稱 GAP 26
CAS 197250-15-0
分子式 C70H107N19O19S
分子量 1550.78
MOL 文件 197250-15-0.mol
更新日期 2026/05/28 07:46:36
197250-15-0 結(jié)構(gòu)式 197250-15-0 結(jié)構(gòu)式

基本信息

中文別名
VR-13
化合物GAP 26
英文別名
GAP 26
GAP-26
GAP26
43Gap 26, Connexin Mimetic
M.W. 1550.78 C70H107N19O19S
Val-Cys-Tyr-Asp-Lys-Ser-Phe-Pro-Ile-Ser-His-Val-Arg
GAP 26/Connexin 43 (63-75) (human, bovine, mouse, rat), Gap Junction α-1 Protein (63-75)
L-Arginine, L-valyl-L-cysteinyl-L-tyrosyl-L-α-aspartyl-L-lysyl-L-seryl-L-phenylalanyl-L-prolyl-L-isoleucyl-L-seryl-L-histidyl-L-valyl-
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

密度1.47±0.1 g/cm3(Predicted)
儲(chǔ)存條件Keep in dark place,Inert atmosphere,2-8°C
溶解度insoluble in EtOH; ≥155.1 mg/mL in H2O with ultrasonic; ≥77.55 mg/mL in DMSO with gentle warming and ultrasonic
酸度系數(shù)(pKa)3.31±0.10(Predicted)
形態(tài)固體
顏色White to off-white
水溶解性Soluble to 2 mg/ml in water
序列H-Val-Cys-Tyr-Asp-Lys-Ser-Phe-Pro-Ile-Ser-His-Val-Arg-OH
InChIKeyFDPIMWZHGJNESB-VCSXYVMHSA-N

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)有害 (GHS07)
GHS07
警示詞警告
危險(xiǎn)性描述H315-H319-H335
WGK GermanyWGK 3
海關(guān)編碼2922498590
存儲(chǔ)類別11 - Combustible Solids

應(yīng)用領(lǐng)域

參考質(zhì)量標(biāo)準(zhǔn)
外觀:白色粉末
純度(HPLC) ≥98.0%
醋酸根含量≤12.0%
水分含量≤8.0%
肽含量≥80.0%
內(nèi)毒素≤50EU/mg
氨基酸組成分析≤±10%

圖譜信息

GAP26價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/03/03S0339GAP26
Gap 26
197250-15-05mg3251.43元
2026/03/03S0339GAP26
Gap 26
197250-15-025mg9819.81元
2025/12/22HY-P1082GAP26
Gap 26
197250-15-01mg900元

常見問題列表

生物活性
Gap 26 是一種連接蛋白模擬肽,由連接蛋白connexin 43 (Cx43)的細(xì)胞外環(huán)1的殘基 no. 63-75組成,是 gap junction 的抑制劑。Gap 26 可阻止光解inositol-1,4,5-trisphosphate觸發(fā)的ATP釋放。
靶點(diǎn)
TargetValue
gap junction
()
體外研究

Gap 26 (0.25 mg/mL, 30 min) reduces the wave size in the three cell lines (RBE4, SV-ARBEC and ECV304). Gap 26 (0.25 mg/mL, 30 min) completely abolishes the InsP3-triggered ATP response and reduced the ATP release to below the control level, indicating that the basal ATP release is also affected.
Gap 26 does indeed significantly inhibit our InsP3-triggered intercellular calcium waves, but it did not have any effect on dye coupling through junctional channels as evidenced by the FRAP experiments, despite the fact that connexin 43 was present in the cell lines used.
Gap 26 (100-300 μM) dose-dependently reduces the rhythmic responses of rabbit superior mesenteric arteries, with IC 50 of 28.4 ± 3.4 μM.

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