Pelagiomicin B

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Category Antibiotics
Catalog number BBF-02377
CAS 173485-81-9
Molecular Weight 383.40
Molecular Formula C20H21N3O5

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Description

It is produced by the strain of Pelagiobacter variabilis.

Specification

Synonyms Antibiotic 2088B; L-Valine, (6-carboxy-4-methoxy-1-phenazinyl)methyl ester
IUPAC Name 6-[[(2S)-2-amino-3-methylbutanoyl]oxymethyl]-9-methoxyphenazine-1-carboxylic acid
Canonical SMILES CC(C)C(C(=O)OCC1=CC=C(C2=NC3=C(C=CC=C3N=C12)C(=O)O)OC)N
InChI InChI=1S/C20H21N3O5/c1-10(2)15(21)20(26)28-9-11-7-8-14(27-3)18-16(11)22-13-6-4-5-12(19(24)25)17(13)23-18/h4-8,10,15H,9,21H2,1-3H3,(H,24,25)/t15-/m0/s1
InChI Key PIEWZDRTLBDIHP-HNNXBMFYSA-N

Properties

Appearance Redorange Needles
Solubility Soluble in Chloroform, Methanol, Butanol

Reference Reading

1. New anticancer antibiotics pelagiomicins, produced by a new marine bacterium Pelagiobacter variabilis
N Imamura, M Nishijima, T Takadera, K Adachi, M Sakai, H Sano J Antibiot (Tokyo). 1997 Jan;50(1):8-12. doi: 10.7164/antibiotics.50.8.
In the course of our screening for new anticancer compounds produced by marine bacteria, we found that a new genus marine bacterium Pelagiobacter variabilis produced new phenazine antibiotics, pelagiomicins A, B and C. Those compounds were labile in water and alcohols. The absolute structure of the main component, pelagiomicin A, and the structures of the minor ones were determined from the spectroscopic data and by synthesis. Pelagiomicin A exhibits activity against Gram-positive and -negative bacteria and antitumor activity in vitro and in vivo.

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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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