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Key Documents

E1310000

Erythromycin B

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

12-Deoxyerythromycin

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About This Item

Fórmula empírica (notación de Hill):
C37H67NO12
Número de CAS:
527-75-3
Peso molecular:
717.93
UNSPSC Code:
41116107
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

erythromycin

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

InChI

1S/C37H67NO12/c1-14-26-20(4)29(40)21(5)28(39)18(2)16-36(9,44)33(50-35-30(41)25(38(11)12)15-19(3)46-35)22(6)31(23(7)34(43)48-26)49-27-17-37(10,45-13)32(42)24(8)47-27/h18-27,29-33,35,40-42,44H,14-17H2,1-13H3/t18-,19?,20+,21+,22?,23-,24?,25?,26-,27?,29+,30?,31+,32?,33-,35?,36-,37?/m1/s1

InChI key

IDRYSCOQVVUBIJ-ZTOAHLHUSA-N

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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Erythromycin B EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

related product

Referencia del producto
Descripción
Precios

PHR1039

Erythromycin, Pharmaceutical Secondary Standard; Certified Reference Material

1242000

Erythromycin, United States Pharmacopeia (USP) Reference Standard

1242010

Erythromycin B, United States Pharmacopeia (USP) Reference Standard

1242021

Erythromycin C, United States Pharmacopeia (USP) Reference Standard

1242032

Erythromycin Related Compound N, United States Pharmacopeia (USP) Reference Standard

1245008

Erythromycin ethyl succinate, United States Pharmacopeia (USP) Reference Standard

E1320000

Erythromycin C, European Pharmacopoeia (EP) Reference Standard

E1400000

Erythromycin estolate, European Pharmacopoeia (EP) Reference Standard

E1500000

Erythromycin ethyl succinate, European Pharmacopoeia (EP) Reference Standard

E1300000

Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard

E1500800

Erythromycin stearate, European Pharmacopoeia (EP) Reference Standard

1243002

Erythromycin estolate, United States Pharmacopeia (USP) Reference Standard

1248006

Erythromycin stearate, United States Pharmacopeia (USP) Reference Standard

1247003

Erythromycin lactobionate, United States Pharmacopeia (USP) Reference Standard

PHR1610

Erythromycin Ethylsuccinate, Pharmaceutical Secondary Standard; Certified Reference Material

BP488

Erythromycin stearate, British Pharmacopoeia (BP) Reference Standard

BP781

Erythromycin, British Pharmacopoeia (BP) Reference Standard

BP889

N-Demethylerythromycin A, British Pharmacopoeia (BP) Reference Standard

BP798

Erythromycin ethyl succinate, British Pharmacopoeia (BP) Reference Standard

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

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Certificados de análisis (COA)

Lot/Batch Number

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Pranab K Bhadra et al.
Journal of medicinal chemistry, 48(11), 3878-3884 (2005-05-27)
Erythromycin A is normally formulated for children as its 2'-ethyl succinate, a taste-free prodrug. Unfortunately, the prodrug hydrolyzes at a measurable rate in the medicine bottle, leading to the vile-tasting erythromycin. We have prepared derivatives of erythromycin B as putative
M S Brown et al.
The Journal of antibiotics, 52(8), 742-747 (1999-12-02)
Cyclopropane carboxylic acid was fed to Saccharopolyspora erythraea NRRL 18643 (6-deoxyerythromycin producer), resulting in the production of 6-deoxy-13-cyclopropyl-erythromycin B. These studies provide further evidence that deoxyerythronolide B synthase has a relaxed specificity for the starter unit.
Q Zhang et al.
Letters in applied microbiology, 52(2), 129-137 (2010-12-24)
To overproduce erythromycin C, B or D and evaluate the effect of disruption of tailoring genes eryK and eryG in an industrial erythromycin producer. The tailoring genes eryG and eryK were inactivated individually or simultaneously by targeted gene disruption in
S Morimoto et al.
The Journal of antibiotics, 43(5), 544-549 (1990-05-01)
6-O-Methylerythromycin B has been synthesized from erythromycin B via regioselective methylation of the 6-hydroxyl group in 71% overall yield. This compound shows in vitro antibacterial activity comparable to erythromycins A and B and exhibits superior in vivo activity with improved
M N Mordi et al.
Journal of medicinal chemistry, 43(3), 467-474 (2000-02-12)
One of the major drawbacks in the use of the antibiotic erythromycin A is its extreme acid sensitivity, leading to degradation in the stomach following oral administration. The modern derivative clarithromycin degrades by a different mechanism and much more slowly.
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