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1202580-59-3

中文名稱(chēng) CAY10618
英文名稱(chēng) CAY10618
CAS 1202580-59-3
分子式 C27H29N5O
分子量 439.55
MOL 文件 1202580-59-3.mol
1202580-59-3 結(jié)構(gòu)式 1202580-59-3 結(jié)構(gòu)式

基本信息

中文別名
化合物 T15412
英文別名
GPP 78
CAY10618
CAY10618 Exclusive
N-(2-phenylphenyl)-8-(4-pyridin-3-yltriazol-1-yl)octanamide
1H-1,2,3-Triazole-1-octanaMide, N-[1,1'-biphenyl]-2-yl-4-(3-pyridinyl)-

物理化學(xué)性質(zhì)

密度1.15±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMF: 10 mg/ml; DMSO: 10 mg/ml; DMSO:PBS(pH 7.2) (1:3): 0.25 mg/ml; Ethanol: 10 mg/ml
酸度系數(shù)(pKa)14.80±0.70(Predicted)
形態(tài)Liquid
顏色Colorless to light yellow

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)易燃 (GHS02)健康危害 (GHS08)
GHS02,GHS08
警示詞危險(xiǎn)
CAY10618價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2025/12/22HY-14374CAY10618
GPP78
1202580-59-31 mg (11.38 mM * 200 μL in Methanol)1150元
2025/12/22HY-14374CAY10618
GPP78
1202580-59-35mg(11.38mM * 1mL in Methanol)3500元

常見(jiàn)問(wèn)題列表

生物活性
GPP78 (CAY10618) 是一種有效的煙酰胺磷酸核糖轉(zhuǎn)移酶 (Nampt) 抑制劑,對(duì) NAD 消耗的 IC50 為 3 nM。GPP78 通過(guò)誘導(dǎo)自噬對(duì)神經(jīng)母細(xì)胞瘤細(xì)胞 SH-SY5Y 具有毒性,IC50 為 3.8 nM。GPP78 具有抗癌和抗炎作用。
靶點(diǎn)

Nampt;
Autophagy

體外研究

GPP78 (Compound 8; 10 nM; 24-40 hours; SH-SY5Y cells) treatment with cells, punctate staining of LC3-II and the formation of autophagolysosomes are observable. LC3-II is membrane-bound and is present in autophagosomes.
GPP78 (Compound 8) inhibits the growth of most cell lines tested, with nanomolar potency (GI 50 ) in cell lines derived from leukemia, lung, CNS, colon, melanoma, ovarian, renal, and prostate cancers. GPP78 appears truly cytotoxic in melanoma cell lines, while in the others it is mainly cytostatic.

Western Blot Analysis

Cell Line: SH-SY5Y cells
Concentration: 10 nM
Incubation Time: 24 hours, 40 hours
Result: Punctate staining of LC3-II and the formation of autophagolysosomes were observable.
體內(nèi)研究

GPP78 (10 mg/kg; intraperitoneal injection; daily; 1 hour or 6 hours after SCI; for 19 days; male adult CD1 mice) treatment reduces the severity of spinal cord trauma in SCI mice.

Animal Model: Male adult CD1 mice (25-30 g) with spinal cord injury (SCI)
Dosage: 10 mg/kg
Administration: Intraperitoneal injection; daily; 1 hour or 6 hours after SCI; for 19 days
Result: Significantly reduced the demyelination associated with SCI. And significantly ameliorated the functional deficits induced by SCI.
"1202580-59-3" 相關(guān)產(chǎn)品信息
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