PMX 53

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Company Name: Nanjing Chemlin Chemical Co., Ltd  
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PMX 53 manufacturers

  • PMX-53
  • PMX-53 pictures
  • $1120.00
  • 2026-01-05
  • CAS:219639-75-5
  • Purity:
  • Supply Ability: 10g
PMX 53 Basic information
Product Name:PMX 53
Synonyms:Ac-Phe-cyclo(Orn-Pro-D-Cha-Trp-Arg);L-Arginine, N-acetyl-L-phenylalanyl-L-ornithyl-L-prolyl-3-cyclohexyl-D-alanyl-L-tryptophyl-, (6→2)-lactam;(S)-N-((3R,6S,9S,15S,20aS)-6-((1H-indol-3-yl)methyl)-3-(cyclohexylmethyl)-9-(3-guanidinopropyl)-1,4,7,10,16-pentaoxoicosahydropyrrolo[1,2-a][1,4,7,10,13]pentaazacyclooctadecin-15-yl)-2-acetamido-3-phenylpropanamide;PMX-53 (3D53);C5aR Antagonist, PMX53
CAS:219639-75-5
MF:C47H65N11O7
MW:896.11
EINECS:
Product Categories:
Mol File:219639-75-5.mol
PMX 53 Structure
PMX 53 Chemical Properties
density 1.40±0.1 g/cm3(Predicted)
storage temp. Store at -20°C, protect from light, stored under nitrogen
solubility Soluble in DMSO
form Solid
pka13.23±0.70(Predicted)
color White to off-white
Water Solubility Soluble to 2 mg/ml in water
SequenceAc-Phe-{Orn}-Pro-{dCha}-Trp-Arg (Lactam bridge: Orn2-Arg6)
Safety Information
WGK Germany WGK 3
Storage Class13 - Non Combustible Solids
MSDS Information
PMX 53 Usage And Synthesis
UsesPMX-53 (3D53) is a synthetic peptidic and a potent and orally active complement C5a receptor (CD88) antagonist with an IC50 of 20 nM. PMX-53 is also a low-affinity MrgX2 agonist that stimulates MrgX2-mediated mast cell degranulation. PMX-53 specifically binds to C5aR1 and does not bind to the second C5aR (C5L2) and C3aR. PMX-53 has anti-inflammatory, anticancer and antiatherosclerotic effects[1][2][3][4][5][6].
Biological ActivityCell permeable: yes', 'Primary Target
C5aR', 'Reversible: yes
in vivo

PMX-53 (0.3-3 mg/kg; subcutaneous injection; once; male Wistar rats) treatment inhibits the hypernociception induced by zymosan-activated serum and C5a but not by the direct-acting hypernociceptive mediators, prostaglandin E2 and dopamine[2].
Local pretreatment of rats with PMX-53 (60-180 μg per paw) inhibits zymosan-, carrageenan-, lipopolysaccharide (LPS)- and antigen-induced hypernociception[2].
Pharmacokinetic analyses have shown that PMX-53 (3D53) appears in the plasma within 5 min of oral administration (3 mg/kg) to rats, with peak blood levels of approximately 0.3 μM being reached within 20 min The plasma elimination half-life was approximately 70 min in this case[3].
The non-acetylated version of PMX-53 (3D53) binds to isolated mouse neutrophils with a Kd value of 30 nM (mouse C5a binds with a Kd value of 0.3 nM) and inhibits mouse C5a-induced chemotaxis with an IC50 value of 0.5 nM[3].

Animal Model:Adult male Wistar rats (weighing 180-200g) injected with zymosan[2]
Dosage:0.3 mg/kg, 1 mg/kg or 3mg/kg
Administration:Subcutaneous injection; once
Result:Inhibited the hypernociception induced by zymosan-activated serum and C5a.
storageStore at -20°C
References[1] Subramanian H, et al. PMX-53 as a dual CD88 antagonist and an agonist for Mas-related gene 2 (MrgX2) in human mast cells. Mol Pharmacol. 2011 Jun;79(6):1005-13. DOI:10.1124/mol.111.071472
[2] Ting E, et al. Role of complement C5a in mechanical inflammatory hypernociception: potential use of C5a receptor antagonists to control inflammatory pain. Br J Pharmacol. 2008 Mar;153(5):1043-53. DOI:10.1038/sj.bjp.0707640
[3] Holland MC, et al. Synthetic small-molecule complement inhibitors. Curr Opin Investig Drugs. 2004 Nov;5(11):1164-73. PMID:15573867
[4] Finch AM, et al. Low-molecular-weight peptidic and cyclic antagonists of the receptor for the complement factor C5a. J Med Chem. 1999 Jun 3;42(11):1965-74. DOI:10.1021/jm9806594
[5] Manthey HD, et al. Complement C5a inhibition reduces atherosclerosis in ApoE-/- mice. FASEB J. 2011 Jul;25(7):2447-55. DOI:10.1096/fj.10-174284
[6] Vadrevu SK, et al. Complement c5a receptor facilitates cancer metastasis by altering T-cell responses in the metastatic niche. Cancer Res. 2014 Jul 1;74(13):3454-65. DOI:10.1158/0008-5472.CAN-14-0157
PMX 53 Preparation Products And Raw materials
Tag:PMX 53(219639-75-5) Related Product Information
PMX 53 acetate(219639755 free base),PMX 53 acetate(219639 75 5 free base) H-Arg-Trp-NH2 2 HCl D-Prolinamide, N-acetyl-L-norleucyl-L-α-aspartyl-L-prolyl-3-(2-naphthalenyl)-D-alanyl-L-arginyl-L-tryptophyl-L-lysyl-D-valyl-, (2→7)-lactam cyclo(L-leucyl-L-tryptophyl) H-LEU-ARG-ARG-TRP-SER-LEU-GLY-OH K-(D-1-Nal)-FwLL-NH2