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Cat. No. | Product Name | Target | Signaling Pathways |
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T7495 |
Hexa-D-arginine
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Others | Others |
Hexa-D-arginine 是稳定的furin 抑制剂,能够作用于 furin (Ki:106 nM)、PACE4 (Ki:580 nM)、PC1 (Ki:13.2 nM)。它在体外和体内均可阻断假单胞菌外毒素 A 和炭疽毒素的毒性。 | |||
TP1160 |
Hexa-D-arginine TFA
Furin Inhibitor II TFA |
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Hexa-D-arginine TFA (Furin Inhibitor II TFA) is an inhibitor of furin (Ki values are 0.106, 0.58 and 13.2 μM for furin, PACE4 and PC1 respectively). | |||
T9964 |
BOS-318
|
Others | Others |
BOS-318是一种Furin 抑制剂,具有缓慢解离,高选择性,细胞通透性等特点。 | |||
T40686 |
Tiazofurin
NSC 286193,Riboxamide,噻唑呋林 |
Dehydrogenase | Metabolism |
Tiazofurin (NSC-286193) 是一种合成的核苷类似物,显示出抗肿瘤活性。 它在细胞内合成为 tiazole-4-carboxamide adenine dinucleotide (TAD),TAD 可有效抑制 IMP 脱氢酶。 | |||
T16690 | Pyrazofurin | Others | Others |
Pyrazofurin is a pyrimidine nucleoside analogue, inhibits cell proliferation and DNA synthesis in cells by inhibiting UMP synthase. Pyrazofurin is a sensitive orotate-phosphoribosyltransferase inhibitor (IC50s between 0.06-0.37 µM in the cell lines Hep-2, | |||
T28744 |
Selenazofurin
BRN 4198668,CI-935,CI 935,CI935 |
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Selenazofurin is an antiviral compound. Selenazofurin inhibits the cytopathic effect and yield of influenza A/NWS/33 virus with 50% effective dose ranges of 0.7 to 1.4 micrograms/ml. | |||
T30002 |
Ammifurin
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Ammifurin is a Furocoumarin mixture used in treatment of vitiligo. | |||
T78121 |
SSM3 tetraTFA hydrate
|
Others | Others |
SSM3 tetraTFA hydrate为有效的furin抑制剂,具有54 nM的EC50和12 nM的Ki。该化合物可有效阻断furin依赖的炭疽毒素保护antigen-83在细胞表面的处理。 | |||
T69640 |
MI-1851
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MI-1851 is a potent peptidomimetic inhibitor. MI-1851could prevent proteolytic processing of the S protein from SARSCoV-2 by endogenous furin in HEK293 cells. | |||
T68339 |
SSM3 TFA
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SSM3 TFA is a potent furin inhibitor, blocking furin-dependent cell surface processing of anthrax protective antigen-83 in vitro.. | |||
T41178 |
SSM 3 trifluoroacetate
|
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SSM 3 trifluoroacetate is a potent furin inhibitor (EC50= 54 nM). Blocks furin-dependent cell surface processing of anthrax protective antigen-83in vitro. | |||
T76607 |
Boc-Arg-Val-Arg-Arg-AMC hydrochloride
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Boc-Arg-Val-Arg-Arg-AMC hydrochloride (Boc-RVRR-AMC) 是一种合成的荧光底物,可被furin 蛋白酶有效裂解。 | |||
TP2038 |
Decanoyl-RVKR-CMK
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Subtilisin/Kex2p-like proprotein convertase inhibitor; blocks activity of all seven convertases (PC1, PC2, PC4, PACE4, PC5, PC7 and furin). Abolishes proET-1 processing in endothelial cells; inhibits regulated secretion of the neuronal polypeptide VGF in | |||
T82592 |
DEC-RVRK-CMK
Decanoyl-Arg-Val-Arg-Lys-chloromethylketone |
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DEC-RVRK-CMK为一种小型合成抗病毒化合物,具不可逆性及细胞渗透性,作为竞争性弗林蛋白酶抑制剂,该化合物对寨卡病毒(ZIKV)和日本脑炎病毒(JEV)显示出显著的抗病毒活性。 | |||
T78224 |
Histatin-3
|
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Histatin-3是一肽类物质,由32个氨基酸残基构成,表现出显著的抗菌活性。作为前蛋白转化酶1(PC1)的底物,Histatin-3在Arg25位点的羧基端被该蛋白酶特异性切割(HRGYR降低SN)。此外,Histatin-3亦作为中等效力的、可逆的以及具竞争性的抑制剂,能够抑制弗林蛋白酶介导的五肽pGlu-Arg-Thr-Lys-Arg-MCA荧光底物的裂解,其抑制常数Ki大约为1.98μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T70221 |
Dibefurin
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Dibefurin is a metabolite that inhibits the activity of calcineurin, a calcium/calmodulin-dependent protein phosphatase involved in the activation of T lymphocytes. |