Demeclocycline hydrochloride
CAS No. 64-73-3
Demeclocycline hydrochloride ( Demethylchlortetracycline; Demethyltetracycline )
产品货号. M15455 CAS No. 64-73-3
A tetracycline antibiotic that acts by binding to the 30S ribosomal subunit to inhibit binding of aminoacyl tRNA which impairs protein synthesis by bacteria.
纯度: >98% (HPLC)
规格 | 价格/人民币 | 库存 | 数量 |
25MG | ¥243 | 有现货 |
|
50MG | ¥348 | 有现货 |
|
100MG | ¥446 | 有现货 |
|
200MG | ¥543 | 有现货 |
|
500MG | ¥656 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Demeclocycline hydrochloride
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述A tetracycline antibiotic that acts by binding to the 30S ribosomal subunit to inhibit binding of aminoacyl tRNA which impairs protein synthesis by bacteria.
-
产品描述A tetracycline antibiotic that acts by binding to the 30S ribosomal subunit to inhibit binding of aminoacyl tRNA which impairs protein synthesis by bacteria; also inhibits the renal action of antidiuretic hormone by interfering with the intracellular second messenger cascade.
-
同义词Demethylchlortetracycline; Demethyltetracycline
-
通路GPCR/G Protein
-
靶点Antibacterial
-
受体30Sribosome
-
研究领域Infection
-
适应症——
化学信息
-
CAS Number64-73-3
-
分子量501.31
-
分子式C21H22Cl2N2O8
-
纯度>98% (HPLC)
-
溶解度10 mM in DMSO
-
SMILESCN(C)[C@H]1[C@@H]2C[C@@H]3[C@@H](C4=C(C=CC(=C4C(=C3C(=O)[C@@]2(C(=C(C1=O)C(=O)N)O)O)O)O)Cl)O.Cl
-
化学全称2-Naphthacenecarboxamide, 7-chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-1,11-dioxo-, hydrochloride (1:1), (4S,4aS,5aS,6S,12aS)-
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
-
Ceforanide
Ceforanide is a second-generation cephalosporin antibiotic with bactericidal activity. Ceforanide causes inhibition of bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall.
-
5-Hydroxysophoranone
5-Hydroxysophoranone is extracted from Erythrina subumbrans stems and exhibits high antiplasmodial activity against Plasmodium falciparum (IC50 = 2.5 μg/mL).
-
NITD-349
NITD-349 is a novel, orally bioavailable mycobacterial membrane protein Large 3 (MmpL3) inhibitor with MIC of 23 nM against M tuberculosis H37Rv.