RCC
Les récepteurs des chimiokines C-C (CCRs) sont un groupe de GPCR qui répondent aux chimiokines, des molécules de signalisation qui guident la migration des cellules immunitaires vers les sites d'inflammation ou d'infection. Les CCR jouent un rôle crucial dans les réponses immunitaires, l'inflammation et le développement de diverses maladies, y compris les troubles auto-immuns et le cancer. La modulation de l'activité des CCR est explorée comme une stratégie thérapeutique pour des affections telles que la polyarthrite rhumatoïde, la sclérose en plaques et l'infection par le VIH. Chez CymitQuimica, nous offrons une gamme de modulateurs de CCR de haute qualité pour soutenir vos recherches en immunologie, inflammation et développement thérapeutique.
154 produits trouvés pour "RCC".
Trier par
Degré de pureté (%)
0
100
|
0
|
50
|
90
|
95
|
100
RP-23618
CAS :RP-23618 is a non-peptidic antagonist of RANTES.Formule :C30H35N5O3S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :577.76VCH-286
CAS :VCH-286 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist.Formule :C34H50F2N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :600.78K777
CAS :K777: Oral cysteine protease inhibitor, CYP3A4 blocker (IC50=60 nM), CCR4 antagonist, anti-Trypanosoma cruzi, antiviral, halts EBOV/SARS-CoV entry (IC50<1 nM).Formule :C32H38N4O4SDegré de pureté :98.43% - 99.14%Couleur et forme :SolidMasse moléculaire :574.73(1S)-CCR2 antagonist 1
CAS :(1S)-CCR2 antagonist 1, a left-handed chiral form of CCR2 antagonist 1, exhibits high affinity and a long residence time as a CCR2 antagonist, with an inhibition constant (K i) of 2.4 nM [1].Formule :C28H32BrF3N2OCouleur et forme :SolidMasse moléculaire :549.47(Rac)-PF-4136309(1341224-83-6 Free base)
CAS :PF-4136309 (INCB8761, PF-04136309) is a highly effective and selective oral CCR2 antagonist with good bioavailability, with an IC50 value of 5.2 nM for humanFormule :C29H31F3N6O3Couleur et forme :SolidMasse moléculaire :568.59SB-649701
CAS :SB-649701 is a potent antagonist of the human CCR8 receptor, exhibiting a pIC50 value of 7.7, and is utilized in asthma research [1].Formule :C27H28N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :456.54PF-04634817 succinate
CAS :PF-0463481 succinate is a potent and orally active dual antagonist of CCR2/CCR5 with comparable human and rodent CCR2 potency with IC50 of 20.8 nM.Formule :C29H42F3N5O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :629.67CMPD167
CAS :CMPD167 (MRK-1) is a potent, orally active inhibitor of CCR5 with significant in vitro antiviral efficacy [1].Formule :C35H47FN4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :574.77cis-J-113863
CAS :Cis-J-113863 is a competitive antagonist for the chemokine receptor 1 (CCR1), demonstrating inhibitory concentration 50 (IC50) values of 0.9 nM for human CCR1 receptors and 5.8 nM for mouse CCR1 receptors, respectively [1].Formule :C30H37Cl2IN2O2Couleur et forme :SolidMasse moléculaire :655.44CCR4 antagonist 4
CAS :CCR4 Antagonist 4 (Compound 22) is a potent and selective antagonist of the CC chemokine receptor-4 (CCR4), displaying an IC50 value of 0.02 μM. It also inhibits MDC-mediated chemotaxis and Ca2+ mobilization, with IC50 values of 0.007 μM and 0.003 μM, respectively. This compound is utilized in research on allergic inflammation [1].Formule :C24H27Cl2N7OCouleur et forme :SolidMasse moléculaire :500.42CCR3 antagonist 1
CAS :CCR3 antagonist 1 is a potent CCR3 antagonist, used for the research of inflammatory and immunologic diseases.Formule :C19H21Cl2N3O4S2Degré de pureté :99.02%Couleur et forme :SolidMasse moléculaire :490.42Ref: TM-T10156
1mg96,00€5mg178,00€1mL*10mM (DMSO)212,00€10mg289,00€25mg462,00€50mg622,00€100mg837,00€INCB3344
CAS :INCB3344 is an effective, specific and orally bioavailable CCR2 antagonist with IC50 values of 9.5 nM (mCCR2) and 5.1 nM (hCCR2) in binding antagonism and 7.8Formule :C29H34F3N3O6Degré de pureté :98% - 98.19%Couleur et forme :SolidMasse moléculaire :577.59Ref: TM-TQ0103
1mg66,00€5mg144,00€1mL*10mM (DMSO)178,00€10mg230,00€25mg358,00€50mg512,00€100mg707,00€200mg973,00€CP-481715
CAS :CP 481715 is an effective selective CCR1 antagonist with potential therapeutic significance for inflammatory diseases.Formule :C26H31FN4O4Couleur et forme :SolidMasse moléculaire :482.55BI 639667
CAS :BI 639667, an azaindazole-class compound, potently inhibits CCR1 (IC50=1.8 nM in calcium flux assays).Formule :C22H18FN5O3SDegré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :451.47Aplaviroc
CAS :Aplaviroc (AK 602), a SDP derivative, is a CCR5 antagonist. With IC50s of 0.1-0.4 nM for HIV-1Ba-L, HIV-1JRFL and HIV-1MOKW.Formule :C33H43N3O6Degré de pureté :98.26% - 99.47%Couleur et forme :SolidMasse moléculaire :577.71YM-344031
CAS :YM-344031 is an orally administered antagonist targeting CCR3. It effectively inhibits the binding of Eotaxin-1 and RANTES to CCR3, with IC50 values of 3.0 and 16.3 nM, respectively. YM-344031 also suppresses ligand-induced increases in intracellular Ca [2+] levels and chemotaxis, alters eosinophil morphology induced by eotaxin-1 in macaque blood, and prevents allergic skin reactions in a mouse allergy model.Formule :C29H31FN4O3Masse moléculaire :502.58CP-865569
CAS :CP-865569 is a CCR1 antagonist useful in the research of inflammatory and autoimmune diseases, including conditions such as rheumatoid arthritis and multiple sclerosis.Formule :C22H26ClFN2O5SCouleur et forme :SolidMasse moléculaire :484.969MK-0812
CAS :MK-0812 is a dual antagonist of the CCR2 and CCR5 receptors that can alleviate adipose inflammation in ob/ob mice.Formule :C24H34F3N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :469.54Nifeviroc
CAS :Nifeviroc (TD-0232) is an orally active CCR5 antagonist, useful in HIV-1 infection research.Formule :C33H42N4O6Degré de pureté :98.14%Couleur et forme :SolidMasse moléculaire :590.71CCR3 antagonist 2
CAS :CCR3 antagonist2 (example 66) is a CCR3 antagonist useful for researching inflammatory or allergic diseases, particularly those affecting the respiratory tract, such as inflammatory or obstructive airway conditions.Formule :C21H28ClN5O3Couleur et forme :SolidMasse moléculaire :433.93
