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Zilucoplan

CAS No.
1841136-73-9
Chemical Name:
Zilucoplan
Synonyms
RA101495;Zilucoplan;Zilucoplan sodium;Poly(oxy-1,2-ethanediyl), α-[2-[[(4S)-4-carboxy-1-oxo-4-(1-oxohexadecyl)butyl]amino]ethyl]-ω-hydroxy-, 15-ether with N-acetyl-L-lysyl-L-valyl-L-α-glutamyl-L-arginyl-L-phenylalanyl-L-α-aspartyl-N-methyl-L-α-aspartyl-3-methyl-L-valyl-L-tyrosyl-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)-L-alanyl-L-α-glutamyl-L-tyrosyl-L-prolyl-(2S)-2-cyclohexylglycyl-N6-(3-hydroxy-1-oxopropyl)-L-lysine (6→1)-lactam
CBNumber:
CB99704201
Molecular Formula:
(C2H4O)nC126H186N24O32
Molecular Weight:
0
MDL Number:
MOL File:
1841136-73-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:59:00

Zilucoplan Properties

form Solid
color White to off-white
FDA UNII YG391PK0CC
NCI Drug Dictionary zilucoplan

Zilucoplan Chemical Properties,Uses,Production

Uses

Zilucoplan (RA101495), a 15-amino acid macrocyclic peptide, is a potent complement component 5 (C5) inhibitor. Zilucoplan can be used in research of immune-mediated necrotising myopathy (IMNM)[1][2].

in vivo

Zilucoplan (RA101495; 10 mg/kg; S.C.; daily, for 6 d) prevents the development of immune-mediated necrotising myopathy (IMNM) in C5-deficient mice supplemented with human complement[1].
Zilucoplan (10 mg/kg; S.C.; daily, for 6 d) has protection on myopathy prevention in C57BL/6 mice[1].

Animal Model:C57BL/10SnJ C5-deficient (C5def) mice with anti-HMGCR+ IMNM IgG xenografts[1]
Dosage:10 mg/kg
Administration:Subcutaneous injection; daily, for 6 days
Result:Prevented muscle strength loss in C5def mice with less complement deposition on myofibres and consequently less necrosis/regeneration.
Animal Model:C57BL/6 mice with anti-HMGCR+ IMNM IgG xenografts[1]
Dosage:10 mg/kg
Administration:Subcutaneous injection; daily, for 6 days
Result:Prevented muscle weakness and reduced regenerated myofibres.
Decreased necrotic cells as well as regenerating cells expressing foetal myosin.

References

[1] Julien S, et, al. Prevention of Anti-HMGCR Immune-Mediated Necrotising Myopathy by C5 Complement Inhibition in a Humanised Mouse Model. Biomedicines. 2022 Aug 20;10(8):2036. DOI:10.3390/biomedicines10082036
[2] Gorman DM, et, al. Chemical synthesis and characterisation of the complement C5 inhibitory peptide zilucoplan. Amino Acids. 2021 Jan;53(1):143-147. DOI:10.1007/s00726-020-02921-5

Zilucoplan Preparation Products And Raw materials

Raw materials

Preparation Products

Zilucoplan Suppliers

Global( 16)Suppliers
Supplier Tel Email Country ProdList Advantage
Apextide Co Ltd
+8615300650552 info@apextide.com China 92 58
Wuhan Jingkang en Biomedical Technology Co., Ltd
+8613720134139 orders@jknbiochem.com China 5221 58
Chongqing jooe co., ltd
+undefined86-15223382610 info@jooe.com China 15976 58
Taizhou Zhongzhi Biotechnology Co., Ltd zhongzhipharma@126.c zhongzhipharma@126.com China 9510 58
Apextide Co Ltd 15300650552 info@apextide.com China 90 58
Shanghai YuanYe Biotechnology Co., Ltd. 021-61312847; 18021002903 3008007409@qq.com China 89686 60
Hangzhou Peptidego Biotech Co.,Ltd. 0571-87213919 Eric@peptidego.com China 7617 58
Hangzhou Sinoda Pharmaceutical Technology Co. LTD 0571-87213919 17306812703 3007955328@qq.com China 7189 58
Wuhan Jingkangen Biomedical Technology Co., Ltd 13720134139 086-15871494362 13720134139 orders@jknbiochem.com China 7080 58
Suzhou Haiben Pharmaceutical Co., Ltd 19353112242 1816280386@qq.com China 8045 58
Zilucoplan RA101495 Poly(oxy-1,2-ethanediyl), α-[2-[[(4S)-4-carboxy-1-oxo-4-(1-oxohexadecyl)butyl]amino]ethyl]-ω-hydroxy-, 15-ether with N-acetyl-L-lysyl-L-valyl-L-α-glutamyl-L-arginyl-L-phenylalanyl-L-α-aspartyl-N-methyl-L-α-aspartyl-3-methyl-L-valyl-L-tyrosyl-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)-L-alanyl-L-α-glutamyl-L-tyrosyl-L-prolyl-(2S)-2-cyclohexylglycyl-N6-(3-hydroxy-1-oxopropyl)-L-lysine (6→1)-lactam Zilucoplan sodium 1841136-73-9