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Merck
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文件

D4065

Supelco

地红霉素

analytical standard, for drug analysis

同義詞:

[9S(R)]-9-脱氧-11-脱氧-9,11-[亚氨[2-(2-甲氧基乙氧基)亚乙基]氧]红霉素;LY-237216

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About This Item

經驗公式(希爾表示法):
C42H78N2O14
CAS號碼:
分子量::
835.07
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:

等級

analytical standard, for drug analysis

品質等級

化驗

≥95% (TLC)

形狀

solid

分子量

apparent mol wt 835.1

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

forensics and toxicology
pharmaceutical (small molecule)
veterinary

格式

neat

SMILES 字串

CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)C4N[C@@H](COCCOC)OC([C@H]4C)[C@]1(C)O

InChI

1S/C42H78N2O14/c1-15-29-42(10,49)37-24(4)32(43-30(56-37)21-52-17-16-50-13)22(2)19-40(8,48)36(58-39-33(45)28(44(11)12)18-23(3)53-39)25(5)34(26(6)38(47)55-29)57-31-20-41(9,51-14)35(46)27(7)54-31/h22-37,39,43,45-46,48-49H,15-21H2,1-14H3/t22-,23-,24+,25+,26-,27+,28+,29-,30-,31+,32+,33-,34+,35+,36-,37-,39+,40-,41+,42-/m1/s1

InChI 密鑰

WLOHNSSYAXHWNR-KZYCBHIHSA-N

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一般說明

Chemical structure: macrolide

應用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

防範說明

危險分類

Skin Sens. 1

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, Faceshields, Gloves


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分析證明 (COA)

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W B Shelley et al.
Journal of the American Academy of Dermatology, 40(1), 69-72 (1999-01-28)
In an open uncontrolled study of 3 patients with balanitis xerotica obliterans we have observed significant improvement after long-term systemic antibiotic therapy. Two of the patients noticed softening of the skin as well as disappearance of pruritus, tenderness, and inflammatory
In vitro activity of azithromycin and dirithromycin against axenic Entamoeba histolytica.
S Ranque et al.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 23(12), 932-933 (2004-12-16)
G G Zhanel et al.
Drugs, 61(4), 443-498 (2001-04-28)
The first macrolide, erythromycin A, demonstrated broad-spectrum antimicrobial activity and was used primarily for respiratory and skin and soft tissue infections. Newer 14-, 15- and 16-membered ring macrolides such as clarithromycin and the azalide, azithromycin, have been developed to address
P A Moore
Journal of the American Dental Association (1939), 130(9), 1341-1343 (1999-09-24)
When treating oral infections, clinicians have used the macrolide antibiotic erythromycin as an alternative antibiotic for patients who have documented allergic reactions to penicillins. In this article, the author reports on his assessment of the pharmacology of erythromycin and the
M M Wasilewski et al.
The Journal of antimicrobial chemotherapy, 46(2), 255-262 (2000-08-10)
We investigated the comparative efficacy and safety of dirithromycin and erythromycin in the treatment of skin and soft tissue infections in this double-blind, randomized, multicentre study, in which 439 patients were randomized to treatment with dirithromycin (500 mg daily for

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