BLASTICIDIN S

BLASTICIDIN S Struktur
2079-00-7
CAS-Nr.
2079-00-7
Englisch Name:
BLASTICIDIN S
Synonyma:
blasticidin;bab;Blas;babs;Blaes;bcs-3;toabla-s;cytovirin;bcs-3、bla-s;blastizidin
CBNumber:
CB2269508
Summenformel:
C17H26N8O5
Molgewicht:
422.45
MOL-Datei:
2079-00-7.mol

BLASTICIDIN S Eigenschaften

Schmelzpunkt:
235°C
Siedepunkt:
539.06°C (rough estimate)
alpha 
D11 +108.4° (water)
Dichte
1.1690 (rough estimate)
Dampfdruck
Low
Brechungsindex
1.6910 (estimate)
Löslichkeit
DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble; Water: soluble
Aggregatzustand
A solid
pka
2.4 (carboxyl), 4.6,8.0 and>12.5 (three bases)
Wasserlöslichkeit
>30 g l-1(20 °C)
Stabilität:
Incompatible with strong oxidizing agents.
EPA chemische Informationen
Blasticidin S (2079-00-7)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T+
R-Sätze: 28
S-Sätze: 24/25-36/37-45
RIDADR  3172
HazardClass  6.1(a)
PackingGroup  II
HS Code  29349990
Giftige Stoffe Daten 2079-00-7(Hazardous Substances Data)
Toxizität LD50 i.v. in mice: 2.82 mg/kg (Takeuchi)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H300 Lebensgefahr bei Verschlucken. Akute Toxizität oral Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS06.jpg" width="20" height="20" /> P264, P270, P301+P310, P321, P330,P405, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P321 Besondere Behandlung
P330 Mund ausspülen.
P405 Unter Verschluss aufbewahren.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

BLASTICIDIN S Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R28:Sehr giftig beim Verschlucken.

S-Sätze Betriebsanweisung:

S24/25:Berührung mit den Augen und der Haut vermeiden.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).

Beschreibung

Nucleoside antibiotic produced by Streptomyces griseochromogenes (1). Biosynthesized from cytosine, glucose, arginine, and methionine (2).

Verwenden

Blasticidin S is a nucleoside produced by several species of Streptomyces, first reported in the late 1950s. Blasticidin S is an antifungal agent with particularly potent activity against the rice pathogen, Piricularia oryzae, for which it was used commercially for some time in Japan. Blasticidin S inhibits protein synthesis and is active against bacteria, tumour cell lines and nematodes. More recently, blasticidin S has been used as a marker for strain manipulations. Blasticidin S provided by BioAustralis is presented as the free base to avoid problems associated with the use of the hydrochloride.

Vorbereitung Methode

Blasticidin S is produced by Streptomyces griseochromogenes, and has a wide range of antimicrobial activity (4). This antibiotic was utilized in the Far East beginning in 1961 against the rice blast pathogen Pyricularia oryzae, with effective control achieved at rates of 10–40 ppm (4).

Definition

ChEBI: A blasticidin that is an antibiotic obtained from Streptomyces griseochromogene.

Allgemeine Beschreibung

Blasticidin S was found in the culture broth of Streptomyces griseochromogenes by Yonehara et al. of the University of Tokyo in 1958. It has a nucleoside-analogue structure and shows strong activity against phytopathogenic fungi, especially Pericularia oryzae, the pathogen causing rice blast. Blasticidin S has been used to protect rice plants.

Pharmakologie

Inhibits protein synthesis both in eukaryotes and in prokaryotes (5,6). Interacts with ribosomal RNA in large subunit, interfering with the transpeptidation step. Inhibits cell-free protein synthesis in P. oryzae and Escherichia coli.

Stoffwechselwegen

Several blasticidin S-resistant microorganisms are found to produce blasticidin S deaminase which catalyzes the hydrolytic deamination of the cytosine moiety in blasticidin S to give a non-toxic deaminohydroxy derivative.

Stoffwechsel

3H-blasticidin S administered to mice was excreted in the urine and feces within 24 h. Cytomycin and cytosin were identified as the main metabolites in and on rice plants, respectively (7). In soil, DT50 < 5 d. Metabolized to nontoxic deaminohydroxy blasticidin S by Aspergillus sp. and resistant Bacillus cereus. Novel deaminase and coding genes, BSD and bsr, were isolated as selectable marker genes for genetic engineering (8).

BLASTICIDIN S Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


BLASTICIDIN S Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 50)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22968 58
career henan chemical co
+86-0371-86658258 15093356674;
factory@coreychem.com China 29826 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167
1026@dideu.com China 9320 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 29220 58
LEAPCHEM CO., LTD.
+86-852-30606658
market18@leapchem.com China 43348 58
Beijing HuaMeiHuLiBiological Chemical 010-56205725
waley188@sohu.com China 12338 58
Shandong Xiya Chemical Co., Ltd. 4009903999 13395398332
sales@xiyashiji.com China 20810 60
Raw material medicin reagent co.,Ltd 025-57798860
sales@njromanme.com China 4534 58
Lynnchem 86-(0)29-85992781 17792393971
info@lynnchem.com China 4587 58

2079-00-7()Verwandte Suche:


  • 1(1’-Cytosinyl)-4-[L-3’-amino-5’(1’’-N-methylguanidino)valerlamino]1,2,3,4-te-tradeoxy-D-erythro-hex-2-enuronicacid
  • Blas
  • Blaes
  • .beta.-D-erythro-Hex-2-enopyranuronic acid, 4-3-amino-5-(aminoiminomethyl)methylamino-1-oxopentylamino-1-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1,2,3,4-tetradeoxy-, (S)-
  • 1(1'-Cytosinyl)-4-[L-3'-amino-5'(1''-N-methylguanidino)valerlamino]1,2,3,4-te-tradeoxy-D-erythro-hex-2-enuronic acid
  • bcs-3、bla-s
  • Alkylate, "hard"
  • Alkylbenzene (branched)
  • Branched alkylbenzene
  • Branched detergent alkylate
  • Branched dodecylbenzene
  • Detergent alkylate (branched)
  • Dodecylbenzene (branched)
  • (2S)-3β-[[(3S)-3-Amino-5-(1-methylguanidino)pentanoyl]amino]-6α-(4-amino-2-oxo-1(2H)-pyrimidinyl)-3,6-dihydro-2H-pyran-2α-carboxylic acid
  • 4-[[(3S)-3-Amino-5-[[amino(imino)methyl]methylamino]-1-oxopentyl]amino]-1-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1,2,3,4-tetradeoxy-β-D-erythro-2-hexenopyranuronic acid
  • 4-[[(S)-3-Amino-5-[(aminoiminomethyl)methylamino]-1-oxopentyl]amino]-1-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1,2,3,4-tetradeoxy-β-D-erythro-2-hexenopyranuronic acid
  • Blastizidin s
  • Blasticidin S Hydrochloride in buffer solutionLiquid
  • Blasticidin S Hydrochloride (solid)
  • 3-(3-amino-5-(1-methylguanidino)-1-oxopentylamino-6-(4-amino-2-oxo-2,3-dihydro-pyrimidin-1-yl)-2,3-dihydro-(6H)-pyran-2-carboxylic acid blasticidin-s
  • S-[4-[3-amino-5-[(aminoiminomethyl) methylamino]-1-oxopentyl] amino]-1-[4-amino-2-oxo-1 (2H)-pyrimidinyl]-1,2,3,4-tetradeoxy-β-D-erythrohex-2-enopyranuronic acid
  • Cytovarin, Bla-S, 21544, A83094C, NSC 91770
  • babs
  • bcs-3
  • blastizidin
  • cytovirin
  • toabla-s
  • Vlasticidins
  • β-D-erythro-Hex-2-enopyranuronic acid, 4-[[(3S)-3-amino-5-[(aminoiminomethyl)methylamino]-1-oxopentyl]amino]-1-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1,2,3,4-tetradeoxy-
  • BLASTICIDIN S USP/EP/BP
  • bab
  • blasticidin
  • BLASTICIDIN S
  • 2079-00-7
  • C17H26N8O5ClH
  • C17H26N8O5
  • FUNGICIDE
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