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D4065

Supelco

地红霉素

analytical standard, for drug analysis

别名:

[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

经验公式（希尔记法）:
C42H78N2O14
CAS号:
62013-04-1
分子量:
835.07
MDL號碼:
MFCD00865041
分類程式碼代碼:
41116107
PubChem物質ID:
329798792

等級

analytical standard, for drug analysis

品質等級

100

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
GHS07

訊號詞

Warning

危險聲明

H317

防範說明

P280

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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分析证书(COA)

Lot/Batch Number
MKCG0791
MKCD2497
MKBV6004V
MKBV2310V
MKBQ6449V

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From the Centers for Disease Control and Prevention. Sudden death in a traveler following halofantrine administration--Togo, 2000.
JAMA, 285(14), 1836-1836 (2001-04-28)
I Moutard et al.
Therapie, 54(5), 607-612 (2000-02-10)
Polymorphonuclear neutrophils are the predominant cells in acute inflammatory lesions and their functions and recruitment are regulated by cytokines, including IL1, TNF and IL8. Antibiotic modulation of inflammatory effects has stimulated investigations of antibiotics for their potential activity as immunomodulators
J Diana et al.
Journal of chromatography. A, 1125(1), 52-66 (2006-06-20)
With a recently developed liquid chromatographic (LC) method, using a phosphate buffer, several unknown impurities present in dirithromycin samples were separated. In this paper, a reversed-phase liquid chromatography-tandem mass spectrometry method is described for the investigation of dirithromycin and related
Yun-Qing Liu et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 864(1-2), 1-8 (2008-02-26)
A sensitive, rapid liquid chromatographic-electrospray ionization mass spectrometric method for determination of erythromycylamine in human plasma was developed and validated. Erythromycylamine in plasma (0.2 mL) was extracted with ethyl acetate, the organic phase was transferred to another clear 1.5 mL
Interactions of macrolide antibiotics (Erythromycin A, roxithromycin, erythromycylamine [dirithromycin], and azithromycin) with phospholipids: computer-aided conformational analyisis and studies on acellular and cell culture models. .
Montenez, J. P., et al.
Toxicology and Applied Pharmacology, 15, 129-129 (1999)
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