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Merck
CN

SBR00119

Sarecycline Hydrochloride

别名:

P-005672 HCl, P005672 HCl

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关于此项目

经验公式(希尔记法):
C24H30ClN3O8
化学文摘社编号:
分子量:
523.96
UNSPSC Code:
51101500
NACRES:
NA.21
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storage condition

under inert gas

Quality Segment

antibiotic activity spectrum

Gram-negative bacteria, Gram-positive bacteria

application(s)

advanced drug delivery

mode of action

protein synthesis | inhibits

shipped in

ambient

storage temp.

2-8°C

SMILES string

CN(C)[C@H]1[C@H]2C[C@H]3CC4=C(C=CC(=C4C(=C3C(=O)[C@@]2(C(=C(C1=O)C(=O)N)O)O)O)O)CN(C)OC.Cl

InChI

1S/C24H29N3O8.ClH/c1-26(2)18-13-8-11-7-12-10(9-27(3)35-4)5-6-14(28)16(12)19(29)15(11)21(31)24(13,34)22(32)17(20(18)30)23(25)33;/h5-6,11,13,18,28-29,32,34H,7-9H2,1-4H3,(H2,25,33);1H/t11-,13-,18-,24-;/m0./s1

InChI key

JGPBDCKZLBSHOI-FIPJBXKNSA-N

General description

Sarecycline Hydrochloride is an antibioitc which belongs to the class of couponds know as tetracycline antibiotics. It is a modified derivative of naturally occurring tetracyclines. Sarecycline Hydrochloride is active against a wide range of Gram-positive and Gram-negative bacteria,

Biochem/physiol Actions

Sarecycline Hydrochloride iinhibits bacterial protein synthesis by binding to the 30S subunit of the bacterial ribosome. Specifically, it binds to the A site of the ribosome and blocks the attachment of aminoacyl-tRNA molecules to the ribosome, which is necessary for the addition of new amino acids to the growing polypeptide chain. This ultimately leads to the inhibition of bacterial protein synthesis and reduction in bacteria that are associated with acne.


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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