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Grahamimycin B

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Grahamimycin B
Category Antibiotics
Catalog number BBF-01276
CAS 75979-94-1
Molecular Weight 300.30
Molecular Formula C14H20O7

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Capabilities & Facilities

Fermentation Lab

4 R&D and scale-up labs

2 Preparative purification labs

Fermentation Plant

Semi pilot, pilot and industrial plant 4 Manufacturing sites 7 Production lines at pilot scale 100+ Reactors of 30-4000 L; 170+ reactors of 20 KL-30 KL; 24+ reactors of >100 KL 2 Hydrogenation reactors (200 L, 4Mpa and 1000L, 4Mpa)

Product Description

It is produced by the strain of Cytospora sp. W. F. P. L. 13A (ATCC20502). It has weak activity against gram-positive bacteria, negative bacteria, cyanobacteria and green algae.

  • Specification
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Synonyms 1,7-Dioxacyclotetradec-3-ene-2,8,11-trione,9,12-dihydroxy-6,14-dimethyl-, (6R-(3E,6R*,9R*,12R*,14S*))-
IUPAC Name (3Z,6R,9R,12R,14S)-9,12-dihydroxy-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione
Canonical SMILES CC1CC=CC(=O)OC(CC(C(=O)CC(C(=O)O1)O)O)C
InChI InChI=1S/C14H20O7/c1-8-4-3-5-13(18)20-9(2)6-10(15)11(16)7-12(17)14(19)21-8/h3,5,8-10,12,15,17H,4,6-7H2,1-2H3/b5-3-/t8-,9+,10-,12-/m1/s1
InChI Key UPKYFPVASUJJTL-NZRRVRCFSA-N
Appearance Colorless Acicular Crystal
Antibiotic Activity Spectrum Gram-positive bacteria; Gram-negative bacteria
Boiling Point 584.3 °C at 760 mmHg
Melting Point 126-127 °C
Density 1.214 g/cm3
Solubility Soluble in Chloroform
1. Grahamimycins: antibiotics from Cytospora sp. Ehrenb. W.F.P.L. 13A
S Gurusiddaiah, R C Ronald Antimicrob Agents Chemother. 1981 Jan;19(1):153-65. doi: 10.1128/AAC.19.1.153.
Aerobic fermentation of cultures of Cytospora sp. Ehrenb. W.F.P.L. 13A produces a group of novel, broad-spectrum, dilactone, macrocyclic antibiotics. These compounds, named grahamimycins, were isolated from the culture medium by extraction with organic solvents and separated by chromatography. Three active components have been obtained in crystalline form and have been designated grahamimycins A, A1, and B. The most active of these, grahamimycin A, exhibited activity against 36 species of bacteria, 8 species of blue-green algae (cyanobacteria), and 2 species of green algae, and antifungal activity against 5 fungi. Studies on the growth of the Cytospora with respect to formation of antibiotic activity, and the isolation, characterization, and structure elucidation of the grahamimycins are described. These studies indicate that the grahamimycins are distinct from other known antibiotics and represent a new class of antibiotic structures.

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Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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