15 Results for "

ACKR3

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "ACKR3" in MCE Product Catalog:

  • Isoforms Recommended:
Cat. No.: HY-123813
CAS No.: 1226686-36-7
Purity:  98.73%
Target:  

CXCR Arrestin

Research Areas:  

Cancer

CCX-777 is an orthosteric binder and partial agonist of CXCR7/ACKR3. CCX-777 induces the recruitment of β-arrestin 2 and affects the rebinding of chemokines to ACKR3. CCX-777 functions to stabilize the ACKR3 receptor and promotes the formation of a monodisperse, stable complex of the receptor in DDM/CHS micelles. CCX-777 is widely used in cancer-related research [3] .
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Cat. No.: HY-RS00162
Research Areas:  

Others

ACKR3 Human Pre-designed siRNA Set A contains three designed siRNAs for ACKR3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P10333A
Target:  

CXCR

LIH383 TFA is an agonist of ACKR3 (CXCR7) (EC50=0.61 nM). LIH383 TFA efficiently induces the recruitment of β-arrestin to ACKR3 but does not trigger typical G protein signaling .
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Cat. No.: HY-D2201
Fluorescent ACKR3 antagonist 1(compound 18a) is a atypical chemokine receptor 3 antagonist .
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Cat. No.: HY-174787
Target:  

mRNA

Research Areas:  

Cancer

Human ACKR3 mRNA encodes the human atypical chemokine receptor 3 (ACKR3) protein, a member of the G-protein coupled receptor family. ACKR3 is a typical chemokine receptor that controls chemokine levels and localization via high-affinity chemokine binding that is uncoupled from classic ligand-driven signal transduction cascades, resulting instead in chemokine sequestration, degradation, or transcytosis.
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Cat. No.: HY-179035
Target:  

Molecular Glues CXCR

Research Areas:  

Cancer

TBS6b is a potent and selective ACKR3 molecular glue degrader. TBS6b degrades ACKR3 via the ubiquitin-proteasome pathway. TBS6b inhibits hepatocellular carcinoma cell proliferation, migration, and invasion. TBS6b is relevant to hepatocellular carcinoma (HCC) research .
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Cat. No.: HY-159582
Target:  

CXCR

Research Areas:  

Cardiovascular Disease

ACKR3 agonist 1 (compound 27) is a selective ACKR3 agonist (EC50=69 nM, Emax=82%) that inhibits platelet aggregation. ACKR3 agonist 1 is metabolically stable and non-cytotoxic, and has the potential to inhibit platelet-mediated thrombosis .
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Cat. No.: HY-RS00163
Research Areas:  

Others

Ackr3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ackr3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS00164
Research Areas:  

Others

Ackr3 Rat Pre-designed siRNA Set A contains three designed siRNAs for Ackr3 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P10333
CAS No.: 2866266-58-0
Target:  

CXCR

LIH383 is an agonist of ACKR3 (CXCR7) (EC50=0.61 nM). LIH383 efficiently induces the recruitment of β-arrestin to ACKR3 but does not trigger typical G protein signaling .
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Cat. No.: HY-161414
Target:  

CXCR

Research Areas:  

Others

trans-VUF25471 (Compound trans-3e) is a photoswitchable ACKR3 agonist. trans-VUF25471 binds and activates ACKR3 at 10-fold lower concentrations compared to its cis-isomer .
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Cat. No.: HY-182533
CAS No.: 3035425-93-2
Target:  

CXCR

Research Areas:  

Cardiovascular Disease

LN5972 is a selective ACKR3 agonist with an EC50 of 3.40 μM, showing higher selectivity for ACKR3 over CXCR4. LN5972 induces β-arrestin recruitment to ACKR3/CXCR7. LN5972 reduces the surface expression of P-selectin. LN5972 is applicable to studies related to platelet-mediated thrombosis .
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Cat. No.: HY-123813A
Target:  

CXCR Arrestin

Research Areas:  

Cancer

CCX-777 formic is an orthosteric binder and partial agonist of CXCR7/ACKR3. CCX-777 formic induces the recruitment of β-arrestin 2 and affects the rebinding of chemokines to ACKR3. CCX-777 formic functions to stabilize the ACKR3 receptor and promotes the formation of a monodisperse, stable complex of the receptor in DDM/CHS micelles. CCX-777 formic is widely used in cancer-related research [3] .
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Cat. No.: HY-184086
CAS No.: 139953-73-4
Research Areas:  

Cancer

Cyclazosin is an α1D-adrenergic receptor antagonist and a partial agonist of CXCR4/ACKR3. The pKi values of Cyclazosin for cloned human α1D, α1B and α1A adrenergic receptors are 9.28, 9.23 and 8.18, respectively. Cyclazosin induces β-arrestin recruitment in CXCR4 and ACKR3 with EC50 values of 16 μM and 10 μM, respectively, stimulates ERK1/2 phosphorylation, and induces receptor internalization. Cyclazosin potently inhibits CXCL12-induced chemotaxis of primary human aortic vascular smooth muscle cells. Cyclazosin alters MDMA-induced thermoregulatory responses in mice, converting monophasic hyperthermia to a biphasic pattern without affecting resting core body temperature. Cyclazosin can be used for diseases related to tumor metastasis, MDMA-induced hyperthermia and vasoconstriction [3] .
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Cat. No.: HY-P700537
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: RDC1; CXCR7; RDC-1; CMKOR1; CXC-R7; CXCR-7; GPR159;
Species:  
Source:  
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