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Merck

M9511

Sigma-Aldrich

米诺环素 盐酸盐

powder, antibiotic

别名:

Minomycin

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About This Item

经验公式(希尔记法):
C23H27N3O7 · HCl
CAS号:
分子量:
493.94
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

product name

米诺环素 盐酸盐, powder

形狀

powder

品質等級

抗生素活性譜

mycobacteria

作用方式

protein synthesis | interferes

起源

Teva

儲存溫度

2-8°C

SMILES 字串

Cl.CN(C)[C@H]1[C@@H]2C[C@@H]3Cc4c(ccc(O)c4C(=O)C3=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O)N(C)C

InChI

1S/C23H27N3O7.ClH/c1-25(2)12-5-6-13(27)15-10(12)7-9-8-11-17(26(3)4)19(29)16(22(24)32)21(31)23(11,33)20(30)14(9)18(15)28;/h5-6,9,11,17,27,29-30,33H,7-8H2,1-4H3,(H2,24,32);1H/t9-,11-,17-,23-;/m0./s1

InChI 密鑰

GLMUAFMGXXHGLU-VQAITOIOSA-N

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一般說明

化学结构:四环素
Minocycline, a semi-synthetic second-generation tetracycline, is classified within the tetracycline class of antibiotics and is utilized for the management and treatment of both infectious and non-infectious conditions. Apart from its efficacy against gram-positive and gram-negative bacteria, minocycline also exhibits antioxidant, anti-apoptotic, immunomodulatory, and neuroprotective properties. Tetracyclines, including minocycline, function by binding to the 30S ribosomal subunit, thereby preventing charged tRNA from delivering amino acids to elongate the protein chain and form cellular protein. This disruption results in a bacteriostatic effect on the prokaryotic cell, leading to the loss of its ability to grow or replicate. Being lipid-soluble compounds, tetracyclines can traverse hydrophobic barriers such as biological membranes. Among tetracyclines, minocycline demonstrates higher lipophilicity than doxycycline, leading to increased concentrations in the central nervous system (CNS) and the skin.

應用

盐酸米诺环素已被用于:
  • 制备纳米脂质体以检查其对巨噬细胞的影响
  • 抑制神经炎症 和神经性疼痛
  • 治疗小鼠GL261胶质瘤细胞胶质瘤

生化/生理作用

米诺环素是一种具有抑菌功能的广谱抗生素。米诺环素具有抗炎作用。米诺环素可抑制脂多糖介导的巨噬细胞炎性细胞因子肿瘤坏死因子(TNF-α )的分泌。米诺环素以剂量依赖性方式抑制巨噬细胞增殖。米诺环素可通过抑制关键的炎症酶(如诱导型一氧化氮合酶(iNOS)、基质金属蛋白酶9(MMP-9)和5-脂氧合酶),从而抑制阿尔茨海默症#8242;样淀粉样蛋白病变前斑块中的神经炎症。米诺环素可抑制内皮细胞增殖和血管生成。米诺环素可通过抑制膜型1基质金属蛋白酶(MT1-MMP)在胶质瘤中表现出抗肿瘤活性。米诺环素可增加认知和神经元分化。 米诺环素可通过增加痛敏肽/孤啡肽FQ的功能有效地减轻神经性疼痛。

特點和優勢

该化合物是由 Teva开发。浏览其他医药开发的化合物和已批准的药物/候选药物清单,请点击此处

包裝

无底玻璃瓶。内含物装在插入的融合锥内。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Minocycline corrects early, pre-plaque neuroinflammation and inhibits BACE-1 in a transgenic model of Alzheimer's disease-like amyloid pathology
Ferretti MT, et al.
Journal of Neuroinflammation, 9(1), 62-62 (2012)
R J Tamargo et al.
Cancer research, 51(2), 672-675 (1991-01-15)
We describe a new inhibitor of angiogenesis, minocycline, a semisynthetic tetracycline antimicrobial with anticollagenase properties. Minocycline was incorporated into controlled release polymers and tested in the rabbit cornea against neovascularization in the presence of the VX2 carcinoma. Inhibition by minocycline
Irene Sanchez-Brualla et al.
Anatomical record (Hoboken, N.J. : 2007), 301(10), 1638-1645 (2018-05-02)
Minocycline has been reported to be both beneficial and detrimental for nerve regeneration after peripheral nerve injury. By reducing the inflammatory response, minocycline administration reduces pain and has neuroprotective effects, but it also inhibits Wallerian degeneration in the distal stump
Minocycline reduces glioma expansion and invasion by attenuating microglial MT1-MMP expression
Markovic DS, et al.
Brain, behavior, and immunity, 25(4), 624-628 (2011)
Jin-Shing Chen et al.
Lancet (London, England), 381(9874), 1277-1282 (2013-03-16)
Simple aspiration and drainage is a standard initial treatment for primary spontaneous pneumothorax, but the rate of pneumothorax recurrence is substantial. We investigated whether additional minocycline pleurodesis after simple aspiration and drainage reduces the rate of recurrence. In our open-label

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