1. Immunology/Inflammation
  2. Complement System
  3. C5aR1 antagonist 1

C5aR1 antagonist 1 (Compound 7e) is an orally active C5a receptor 1 (C5aR1) antagonist. C5aR1 antagonist 1 is active in DISCO and migration assays, with IC50 values of 38 nM and 17 nM, respectively. C5aR1 antagonist 1 can be used for the research of acute and chronic inflammatory diseases.

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C5aR1 antagonist 1 Chemical Structure

C5aR1 antagonist 1 Chemical Structure

CAS No. : 2365325-67-1

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Description

C5aR1 antagonist 1 (Compound 7e) is an orally active C5a receptor 1 (C5aR1) antagonist. C5aR1 antagonist 1 is active in DISCO and migration assays, with IC50 values of 38 nM and 17 nM, respectively. C5aR1 antagonist 1 can be used for the research of acute and chronic inflammatory diseases[1].

IC50 & Target

C5aR1

 

In Vitro

C5aR1 antagonist 1 (compound 7e) is a surmountable and competitive antagonist of C5aR, with the KD value of 15 nM[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

The pharmacokinetic profile of C5aR1 antagonist 1 (compound 7e) (10/30/50 mg/kg, single administration) in vivo in rat, dog, and cynomolgus monkey indicates that the low solubility of the compound waslimiting the exposure[1].
C5aR1 antagonist 1 (1/3/10 mg/kg, administered orally 2/8/16h before blood sampling for neutrophil quantification) dose-dependent inhibits the increase of neutrophils in the blood of the neutrophilic rat model[1].
C5aR1 antagonist 1 (0/1/3/10/30 mg/kg, administered orally 2 h before blood sampling) inhibites the upregulation of CD11b of the female hC5aR1 knock-in rats by around 90%[1].

Pharmacokinetic Properties of Compound 7e[1]

Animals Route Dose (mg/kg) CL mL/(min×kg) Vss_obs (L/kg) T1/2 (h) AUC0‑last (ng×h)/mL Cmax (ng×h)/mL Tmax (h)
rat p.o. 10 39 7.1 4.1 32200 3890 2
dog p.o. 30 2.3 7.6 1.1 14900 2530 1
monkey p.o. 50 3500 635 2 41900 3940 4

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Neutrophilia Rat Model[1]
Dosage: 1/3/10 mg/kg
Administration: Oral gavage (p.o.), Rats were administered po with compound or vehicle at 23.5/15.5/7.5/1.5 h before hC5a iv injection.
Result: Inhibited reactive neutrophilia induced by hC5a administration in vivo.
Molecular Weight

497.53

Formula

C28H27F4N3O

CAS No.
SMILES

O=C1N(CC2=C(C(F)(F)F)C=CC=C2)C3=C(CN1C4CCN(CC4)C5=C(C)C=CC=C5F)C=CC=C3

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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C5aR1 antagonist 1 Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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C5aR1 antagonist 1
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HY-163378
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