FOY-251 mesylate chemical structure
Chemical structureResearch use only
CAT. NO. DC26121Featured

FOY-251 mesylate

Pack Sizes & Prices

TotalUS$700
We match the best price and quality on market.
Product overview

Description & Application

FOY 251 is an anti-proteolytic active metabolite camostate (HY-13512), acts as a proteinase inhibitor[1].

ParameterValue
Chemical Name4-[[4-[(Aminoiminomethyl)amino]benzoyl]oxy]-benzeneacetic Acid Monomethanesulfonate
CAS No.71079-09-9
SynonymsFOY-251 mesylate,FOY 251 mesylate FOY251 mesylate
FormulaC17H19N3O7S
M.Wt409.41
SMILESCS(=O)(=O)O.C1=CC(=CC=C1CC(=O)O)OC(=O)C2=CC=C(C=C2)N=C(N)N
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

FOY 251 is an anti-proteolytic active metabolite camostate (HY-13512), acts as a proteinase inhibitor[1].

In Vitro

FOY-251 represents a dose-dependent inhibition of equivalent current in M-1 cells[2]. FOY-251 inhibits the proteolytic activity of prostasin[2].

In Vivo

No in vivo data are provided in the current product source. Contact us for further information.

References & source

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Solution calculator

Related research products

Telaprevir (VX-950) chemical structureDC1008

Telaprevir (VX-950)

Telaprevir is a highly selective, reversible, and potent peptidomimetic inhibitor of the HCV NS3-4A protease, the steady-state inhibitory constant (Ki) of Telaprevir is 7 nM against a genotype 1 (H strain) NS3 protease…

View activity & prices
Favipiravir (T-705) chemical structureDC5105

Favipiravir (T-705)

Favipiravir is a novel viral RNA polymerase inhibitor, it is phosphoribosylated by cellular enzymes to its active form, Favipiravir-ribofuranosyl-5′-triphosphate (RTP). Favipiravir-RTP inhibits the influenza viral…

View activity & prices
TDZD-8 chemical structureDC2067

TDZD-8

TDZD-8 is an inhibitor of GSK-3β, with an IC50 of 2 μM; TDZD-8 shows less potent activities against Cdk-1/cyclin B, CK-II, PKA, and PKC, with all IC50s of >100 μM.

View activity & prices
EIDD-1931(NHC) chemical structureDC21382

EIDD-1931(NHC)

Beta-d-N4-hydroxycytidine (NHC) is a nucleoside analogue that has antipestivirus and antihepacivirus activities; inhibits the production of cytopathic BVDV RNA with EC90 of 5.4 uM, also has an EC50 of 5 uM for replicon…

View activity & prices
Remdesivir(GS-5734) chemical structureDC11735

Remdesivir(GS-5734)

Remdesivir(GS-5734) is a nucleoside analogue, with effective antiviral activity, with EC50s of 74 nM for ARS-CoV and MERS-CoV in HAE cells, and 30 nM for murine hepatitis virus in delayed brain tumor cells.

View activity & prices
PX 12 chemical structureDC7992

PX 12

PX-12(IV-2) is an irreversible inhibitor of Thioredoxin-1 (Trx-1); inhibits the growth of MCF-7 and HT-29 cells with IC50 values of 1.9 and 2.9 μM, respectively.

View activity & prices

Cart

Request quotation