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CCR

CC chemokine receptors (or beta chemokine receptors) are integral membrane proteins that specifically bind and respond to cytokines of the CC chemokine family. They represent one subfamily of chemokine receptors, a large family of G protein-linked receptors that are known as seven transmembrane (7-TM) proteins since they span the cell membrane seven times. To date, ten true members of the CC chemokine receptor subfamily have been described. These are named CCR1 to CCR10 according to the IUIS/WHO Subcommittee on Chemokine Nomenclature.
Cat. No. 製品名 CAS No. Purity Chemical Structure
T60336 CCR4 antagonist 3-1 1957-01-3 98%
CCR4 antagonist 3-1 is a less active chemokine receptor 4 (CCR4) antagonist that inhibits [125I]TARC (thymus and activation-regulated chemokine) with an IC50 val...
T3188 NSC5844 140926-75-6 98%
NSC5844 (RE640) is a bisquinoline compound with C-C chemokine receptor type 1 (CCR1)-agonistic activities.
T13114 CCR2 antagonist 4 226226-39-7 98%
CCR2 antagonist 4 is a potent and specific antagonist of CCR2(IC50s of 180 nM), and potently inhibits MCP-1-induced chemotaxis(IC50 of 24 nM).
T14688 BMS CCR2 22 445479-97-0 98%
BMS CCR2 22 is a potent and selective antagonist of CCR2 with calcium flux IC50 of 18 nM, chemotaxis IC50 of 1 nM, and binding IC50 of 5.1 nM.
TN1599 Eburicoic acid 560-66-7 98%
Eburicoic acid exhibits anti-inflammatory and antioxidant activity thereby protecting the liver from CCl4-induced hepatic damage and can be used in studies about...
T4674 SB297006 58816-69-6 98%
SB 297006 is an antagonist of C-C chemokine receptor 3 (CCR3; IC50 = 39 nM), which normally is activated by eotaxin, eotaxin-3, MCP-3, MCP-4, RANTES, and MIP-1δ....
T3327 Artemotil 75887-54-6 98%
Arteether is a new, fast-acting antimalarial drug.
T11699 J-113863 353791-85-2 98%
J-113863 is also a potent antagonist of the human CCR3 (IC50 of 0.58 nM) , but a weak antagonist of the mouse CCR3 (IC50 of 460 nM). J-113863 is inactive against...
T15253 CCX354 1010073-75-2 98%
CCX354 is a potent small molecule CCR1 antagonist with anti-inflammatory activity for the treatment of rheumatoid arthritis.
T7624 DAPTA 106362-34-9 98%
DAPTA(TFA) is an inhibitor of CCR5, shows potent anti-HIV activities.
T10712 CCR2 antagonist 3 1380100-86-6 98%
CCR2 antagonist 3 is an antagonist of CCR2.
T21870 C-021 864289-85-0 98%
C 021 dihydrochloride is a potent CCR4 antagonist. C-021 dihydrochloride potently inhibits functional chemotaxis in humans and mice with IC50s of 140 nM and 39 n...
T30260 AZD-5672 780750-65-4 98%
AZD-5672 is an antagonist of CCR5 with an IC50 of 0.32 nM. AZD-5672 inhibits hERG cardiac ion channel binding and P-gp-mediated digoxin transport with IC50s of 7...
T9983 CCR8 antagonist 1 723304-76-5 98%
CCR8 antagonist 1 is an antagonist of C-C Motif Chemokine Receptor 8 (CCR8) with a Ki value of 1.6 nM.
T3435 Vicriviroc maleate 599179-03-0 98%
Vicriviroc maleate(Sch-417690) is a piperazine-based CCR5 receptor antagonist with activity against human immunodeficiency virus. The IC50 value is 0.91 nM in cl...
T14909 CCX140 1100318-47-5 98%
CCX140 (CCX140-B) is an antagonist of CCR2.
T24700 R243 688352-84-3 98%
R243 is CCR8 signaling and chemotaxis inhibitor.
TQ0103 INCB3344 1262238-11-8 98%
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 7.8 nM...
T10425 AZ084 929300-19-6 98%
AZ084 is a potent, selective, allosteric, and oral active CCR8 antagonist (Ki: 0.9 nM). It has the potential to treat asthma.
T10708 CCR1 antagonist 6 2436773-01-0 98%
CCR1 antagonist 6 is a CCR1 antagonist (IC50: 3 nM).
CCR4 antagonist 3-1
T60336
CCR4 antagonist 3-1 is a less active chemokine receptor 4 (CCR4) antagonist that inhibits [125I]TARC (thymus and activation-regulated chemokine) with an IC50 val...
NSC5844
T3188
NSC5844 (RE640) is a bisquinoline compound with C-C chemokine receptor type 1 (CCR1)-agonistic activities.
CCR2 antagonist 4
T13114
CCR2 antagonist 4 is a potent and specific antagonist of CCR2(IC50s of 180 nM), and potently inhibits MCP-1-induced chemotaxis(IC50 of 24 nM).
BMS CCR2 22
T14688
BMS CCR2 22 is a potent and selective antagonist of CCR2 with calcium flux IC50 of 18 nM, chemotaxis IC50 of 1 nM, and binding IC50 of 5.1 nM.
Eburicoic acid
TN1599
Eburicoic acid exhibits anti-inflammatory and antioxidant activity thereby protecting the liver from CCl4-induced hepatic damage and can be used in studies about...
SB297006
T4674
SB 297006 is an antagonist of C-C chemokine receptor 3 (CCR3; IC50 = 39 nM), which normally is activated by eotaxin, eotaxin-3, MCP-3, MCP-4, RANTES, and MIP-1δ....
Artemotil
T3327
Arteether is a new, fast-acting antimalarial drug.
J-113863
T11699
J-113863 is also a potent antagonist of the human CCR3 (IC50 of 0.58 nM) , but a weak antagonist of the mouse CCR3 (IC50 of 460 nM). J-113863 is inactive against...
CCX354
T15253
CCX354 is a potent small molecule CCR1 antagonist with anti-inflammatory activity for the treatment of rheumatoid arthritis.
DAPTA
T7624
DAPTA(TFA) is an inhibitor of CCR5, shows potent anti-HIV activities.
CCR2 antagonist 3
T10712
CCR2 antagonist 3 is an antagonist of CCR2.
C-021
T21870
C 021 dihydrochloride is a potent CCR4 antagonist. C-021 dihydrochloride potently inhibits functional chemotaxis in humans and mice with IC50s of 140 nM and 39 n...
AZD-5672
T30260
AZD-5672 is an antagonist of CCR5 with an IC50 of 0.32 nM. AZD-5672 inhibits hERG cardiac ion channel binding and P-gp-mediated digoxin transport with IC50s of 7...
CCR8 antagonist 1
T9983
CCR8 antagonist 1 is an antagonist of C-C Motif Chemokine Receptor 8 (CCR8) with a Ki value of 1.6 nM.
Vicriviroc maleate
T3435
Vicriviroc maleate(Sch-417690) is a piperazine-based CCR5 receptor antagonist with activity against human immunodeficiency virus. The IC50 value is 0.91 nM in cl...
CCX140
T14909
CCX140 (CCX140-B) is an antagonist of CCR2.
R243
T24700
R243 is CCR8 signaling and chemotaxis inhibitor.
INCB3344
TQ0103
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 7.8 nM...
AZ084
T10425
AZ084 is a potent, selective, allosteric, and oral active CCR8 antagonist (Ki: 0.9 nM). It has the potential to treat asthma.
CCR1 antagonist 6
T10708
CCR1 antagonist 6 is a CCR1 antagonist (IC50: 3 nM).
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