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7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-trien-1,20,23-trion

CYTOCHALASIN A Struktur
14110-64-6
CAS-Nr.
14110-64-6
Bezeichnung:
7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-trien-1,20,23-trion
Englisch Name:
CYTOCHALASIN A
Synonyma:
Dehydrophomin;CYTOCHALASIN A;CYTOCHALASIN A(RG);5,5-Didehydrophomin;Cytochalasin dreschslera dematioidea;CYTOCHALASIN A FROM DRESCHSLERA DEMATIOIDEA;CytochalasinA from Drechslera dematioidea;cytochalasin a from helminthosporium dematioideum;Cytochalasin A from Drechslera dematioidea;Cytochalasin A 5-Dehydrophomin Dehydrophomin
CBNumber:
CB6735221
Summenformel:
C29H35NO5
Molgewicht:
477.59
MOL-Datei:
14110-64-6.mol

7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-trien-1,20,23-trion Eigenschaften

Schmelzpunkt:
190-191 °C
Siedepunkt:
725.1±60.0 °C(Predicted)
Dichte
1.20±0.1 g/cm3(Predicted)
storage temp. 
-20°C
L?slichkeit
ethanol: 20 mg/mL, clear, colorless
pka
13.54±0.70(Predicted)
Aggregatzustand
Powder
Farbe
White
Wasserl?slichkeit
Soluble in DMF, DMSO, ethanol and acetone. Insoluble in water.
Sensitive 
Light Sensitive
BRN 
949521
InChIKey
ZMAODHOXRBLOQO-TZVKRXPSSA-N
SMILES
C[C@@H]1CCCC(=O)\C=C\C(=O)O[C@]23[C@@H](\C=C\C1)[C@H](O)C(=C)[C@@H](C)[C@H]2[C@H](Cc4ccccc4)NC3=O
LogP
1.849 (est)
EPA chemische Informationen
Cytochalasin A (14110-64-6)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher T+,T
R-S?tze: 26/27/28-63
S-S?tze: 28-36/37-45
RIDADR  UN 1544 6.1/PG 2
WGK Germany  3
10
HazardClass  6.1(a)
PackingGroup  I
HS Code  29349990
Speicherklasse 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 1 Inhalation
Acute Tox. 2 Dermal
Acute Tox. 2 Oral
Repr. 2
Bildanzeige (GHS) Skull and Crossbones (GHS06)Health Hazard (GHS08)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H361 Kann vermutlich die Fruchtbarkeit beeintr?chtigen oder das Kind im Mutterleib sch?digen. Reproduktionstoxizit?t Kategorie 2 Warnung P201, P202, P281, P308+P313, P405,P501
Sicherheit
P201 Vor Gebrauch besondere Anweisungen einholen.
P202 Vor Gebrauch alle Sicherheitshinweise lesen und verstehen.
P260 Dampf/Aerosol/Nebel nicht einatmen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-trien-1,20,23-trion Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R26/27/28:Sehr giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R63:Kann das Kind im Mutterleib m?glicherweise sch?digen.

S-S?tze Betriebsanweisung:

S28:Bei Berührung mit der Haut sofort abwaschen mit viel . . . (vom Hersteller anzugeben).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).

Beschreibung

The cytochalasins are cell-permeable fungal metabolites which inhibit actin polymerization. This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion. Cytochalasin A is an oxidized analog of cytochalasin B which uniquely inhibits HIV-1 protease (IC50 = 3 μM). Cytochalasins A and B differ from other cytochalasins in being able to rapidly and reversibly inhibit glucose transport by competitively binding glucose transporters (Ki = 4.0 and 0.6 μM, respectively). Cytochalasin A also induces the phosphorylation of the tyrosine phosphatase PTP3 of Dictyostelium, activating STATc.

Chemische Eigenschaften

white powder

Verwenden

Cytochalasin A is one of a family of potent mycotoxins produced by several species of fungi. All members of the class exhibit profound effects on cytoskeletal proteins, giving rise to pronounced morphogenic activity in animals and plants. Like most cytochalsins, cytochalasin A exhibits potent inhibition of actin filament function leading to cell death by apoptosis, and displays a broad range of resultant cellular actions. Despite the common mode of action, there is evidence that individual members of the class display diverse selectivity. Specifically, cytochalasin A is one of the few cytochalasins exhibiting activity against HIV-1 protease.

7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-trien-1,20,23-trion Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-trien-1,20,23-trion Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 114)Lieferanten
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TargetMol Chemicals Inc.
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Sigma-Aldrich 021-61415566 800-8193336
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Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627
info@efebio.com China 9804 58
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3008007409@qq.com China 89686 60

14110-64-6(7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-trien-1,20,23-trion)Verwandte Suche:


  • (7S,13E,16R,21E)-7-Hydroxy-16-methyl-10-phenyl-24-oxa[14]cytochalasa-6(12),13,21-triene-1,20,23-trione
  • 5,5-Didehydrophomin
  • Dehydrophomin
  • Cytochalasin dreschslera dematioidea
  • Cytochalasin A 5-Dehydrophomin Dehydrophomin
  • 7(S)-hydroxy-16(R)-methyl-10-phenyl-24-oxa[14]cytochalasa-6(12),13(E),21(E)-triene-1,20,23-trione
  • 2H-Oxacyclotetradecino2,3-disoindole-2,5,18-trione, 6,7,8,9,10,12a,13,14,15,15a,16,17-dodecahydro-13-hydroxy-9,15-dimethyl-14-methylene-16-(phenylmethyl)-, (3E,9R,11E,12aS,13S,15S,15aS,16S,18aS)-
  • CYTOCHALASIN A FROM DRESCHSLERA DEMATIOIDEA
  • CYTOCHALASIN A FROM DRESCHSLERA DEMATIOIDEA, BIOCHEMIKA, >= 99.0% (TLC)
  • CYTOCHALASIN A
  • cytochalasin a from helminthosporium dematioideum
  • CYTOCHALASIN A(RG)
  • CytochalasinA from Drechslera dematioidea
  • Cytochalasin A from Drechslera dematioidea
  • 14110-64-6
  • C29H35NO5
  • Other
  • Cytoskeleton and Extracellular Matrix
  • Enzymes, Inhibitors, and Substrates
  • Enzyme Inhibitors
  • Enzyme Inhibitors by Type
  • Cell Biology
  • Cell Signaling and Neuroscience
  • Biochemicals and Reagents
  • BioChemical
  • Actin Inhibitors and Probes
  • Actin Inhibitors and ProbesCell Signaling and Neuroscience
  • Cell Signaling and Neuroscience
  • antibiotic
  • Cytoskeleton and Extracellular Matrix
  • Mold
  • Toxins and Venoms
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