Catalog |
name |
Description |
price |
R-M-561 |
Acetyl-(N-methyl)tyrosyl-valyl-alanyl-asparta |
Acetyl-(N-methyl)tyrosyl-valyl-alanyl-asparta,Ac-N-Me-Tyr-Val-Ala-Asp-aldehyde (pseudo acid)(CAS : 160806-26-8) from ruixi.It is an inhibitory peptide. |
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R-M-568 |
Ac-Pen-Arg-Gly-Asp-Cys-OH (Disulfide bond) |
The cyclic RGD-containing pentapeptide Ac-PenRGDC has been demonstrated to be a potent inhibitor of blood platelet aggregation (IC50 = 0.55 µM). |
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R-M-570 |
Ac-Phe-Lys-OH |
Ac-Phe-Lys-OH,CAS:14287-21-9 is a Inverted aspartame-type sweetener. Ac-Phe-Lys-OH can be used as targeted mTOR inhibitors. Adrover et al. used Ac-Phe-Lys as a model compound in their studies on protein glycation. |
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R-M-581 |
Ac-Val-Glu-Ile-Asp-aldehyde (pseudo acid) |
Ac-Val-Glu-Ile-Asp-aldehyde (pseudo acid),Ac-VEID-CHO(CAS :319494-39-8) is an inhibitor of caspase-6 (IC50 = 16.2 nM). It is selective for caspase-6 over caspase-7 (IC50 = 162.1 nM) but can also inhibit caspase-3 (IC50 = 13.6 nM). |
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R-M-613 |
Adrenomedullin (22-52) (human) trifluoroacetate salt |
Adrenomedullin (22-52) (human) trifluoroacetate salt,CAS:159899-65-7 from ruixi.ADM (22-52) is a putative adrenomedullin receptor antagonist that inhibits the production of cAMP elicted by adrenomedullin. It is a more effective antagonist for adrenomedullin- and CGRP-specific receptors than α-CGRP (8-37) (human). |
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R-M-636 |
H-Ala-Ala-Phe-chloromethylketone·TFA |
H-Ala-Ala-Phe-chloromethylketone·TFA (CAS: 184901-82-4) is a serine protease inhibitor. |
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R-M-643 |
H-Ala-Trp-OH |
The dipeptide AW(H-Ala-Trp-OH) is a non-competitive inhibitor of angiotensin-1 converting enzyme (ACE). |
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R-M-645 |
H-Ala-Tyr-OH |
H-Ala-Tyr-OH(CAS:3061-88-9) is Inhibitor of angiotensin-1 converting enzyme (ACE). Ala-Tyr has been used as a tyrosine source in intravenous nutrition of the rat. The dipeptide AY is an efficient Tyr source for the parenteral nutrition of patients with hepatic failure. |
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R-M-665 |
Anti-Inflammatory Peptide 2 |
Anti-Inflammatory Peptide 2,CAS:118850-72-9 from ruixi.It is a kind of Inhibitor of phospholipase A2.It can be used for Inflammation Research. |
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R-M-668 |
Diazepam Binding Inhibitor (DBI) Fragment (human) |
Diazepam Binding Inhibitor (DBI) Fragment (human) ,CAS: 104360-70-5 from ruixi.DBI (51-70), QATVGDINTERPGMLDFTGK, is also called eikosaneuropeptide (ENP). |
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