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(+)-Brefeldin A

Brefeldin A Struktur
20350-15-6
CAS-Nr.
20350-15-6
Bezeichnung:
(+)-Brefeldin A
Englisch Name:
Brefeldin A
Synonyma:
BFA;Brefeldin;CYANEIN;(+)-BREFELDIN A;CS-766;DECUMBIN;cyanaein;ASCOTOXIN;NSC 89671;NECTROLIDE
CBNumber:
CB0689753
Summenformel:
C16H24O4
Molgewicht:
280.36
MOL-Datei:
20350-15-6.mol

(+)-Brefeldin A Eigenschaften

Schmelzpunkt:
200-205 °C
Siedepunkt:
492.7±45.0 °C(Predicted)
alpha 
93 º (C=2 IN MEOH)
Dichte
1.108±0.06 g/cm3(Predicted)
Dampfdruck
0.56 hPa ( 20 °C)
Flammpunkt:
87 °C
storage temp. 
Sealed in dry,Store in freezer, under -20°C
L?slichkeit
methanol: 10 mg/mL, clear, colorless to faintly yellow
pka
12.92±0.60(Predicted)
Aggregatzustand
Crystalline Powder
Farbe
White to almost white
Biologische Quelle
Penicillium brefeldianum
Wasserl?slichkeit
Soluble in dimethylsulfoxide, dichloromethane and ethanol. Slightly soluble in water.
Merck 
13,1355
BRN 
25191
Stabilit?t:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
InChI
1S/C16H24O4/c1-11-5-3-2-4-6-12-9-13(17)10-14(12)15(18)7-8-16(19)20-11/h4,6-8,11-15,17-18H,2-3,5,9-10H2,1H3/b6-4+,8-7+/t11-,12+,13-,14+,15-/m0/s1
InChIKey
QSECOIOBNZLGOD-OBCVZTHZSA-N
SMILES
O1[C@H](CCC\C=C\[C@H]2[C@H]([C@H](\C=C\C1=O)O)C[C@H](C2)O)C
CAS Datenbank
20350-15-6
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn,T
R-S?tze: 22-25-36/37/38-20/21/22
S-S?tze: 24/25-45-36-26
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS-Nr. GY8410000
Selbstentzündungstemperatur 301 °C
HS Code  29411090
Speicherklasse 10 - Combustible liquids
Toxizit?t LD50 i.p. in mice: >200 mg/kg (Haerri)
Bildanzeige (GHS) Skull and Crossbones (GHS06)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H301 Giftig bei Verschlucken. Akute Toxizit?t oral Kategorie 3 Achtung P264, P270, P301+P310, P321, P330,P405, P501
Sicherheit
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.

(+)-Brefeldin A Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R22:Gesundheitssch?dlich beim Verschlucken.
R25:Giftig beim Verschlucken.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
R20/21/22:Gesundheitssch?dlich beim Einatmen,Verschlucken und Berührung mit der Haut.

S-S?tze Betriebsanweisung:

S24/25:Berührung mit den Augen und der Haut vermeiden.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Chemische Eigenschaften

White Powder

Verwenden

Brefeldin A is a potent inhibitor of cell growth first described in 1958, then independently rediscovered by several groups as a potent active in a broad range of bioassays. Brefeldin has antiviral, antibiotic, antifungal, antitumour and herbicidal activity. Early studies on the mode of action of brefeldin identified inhibition of protein and nucleic acid synthesis by disruption of the Golgi apparatus. The precise molecular target is a subset of Sec7-type GTP exchange factors (GEFs) that activate a small GTPase, Arf1p, an integral component of protein trafficking and signalling.

Definition

ChEBI: A metabolite from Penicillium brefeldianum that exhibits a wide range of antibiotic activity.

Allgemeine Beschreibung

Specifically and reversibly blocks translocation of proteins from the endoplasmic reticulum (ER) to the Golgi apparatus without affecting endocytosis or lysosome function. Inhibitor of HDL-mediated cholesterol efflux. Causes disassembly of the Golgi complex and ER swelling in a variety of mammalian cell lines at <40 ng/ml. Blocks binding of ADP-ribosylation factor to the Golgi and inhibits the GDP-GTP exchange. Inhibits the activity of BIG1 and BIG2, the guanine-nucleotide exchange proteins for ADP-ribosylation factors. Also available as a 25 mM solution in DMSO (Cat. No. 500583).

Biologische Aktivit?t

Reversible inhibitor of protein translocation from the endoplasmic reticulum (ER) to the Golgi apparatus. Blocks binding of ADP-ribosylation factor to the Golgi apparatus and inhibits GDP-GTP exchange.

l?uterung methode

Brefeldin A was isolated from Penicillium brefeldianum and recrystallised from aqueous MeOH/EtOAc or MeOH. Its solubility in H2O is 0.6mg/mL, 10mg/mL in MeOH and 24.9mg/mL in EtOH. The O-acetate recrystallises from Et2O/pentane and has m 130-131o, [] D +17o (c 0.95, MeOH). [Sigg Helv Chim Acta 47 1401 1964, UV and IR: H.rri et al. Helv Chim Acta 46 1235 1963, total synthesis: Kitahara et al. Tetrahedron 3021 1979, X-ray : Weber et al. Helv Chim Acta 54 2763 1971, Beilstein 18 III/IV 1220.]

(+)-Brefeldin A Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


(+)-Brefeldin A Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 328)Lieferanten
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20350-15-6((+)-Brefeldin A)Verwandte Suche:


  • NSC 107456
  • (1R,2E,6S,10E,11aS,13S,14aR)-1,13-dihydroxy-6-Methyl-6,7,8,9,12,13,14,14a-octahydro-1H-cyclopenta[f][1]oxacyclotridecin-4(11aH)-one
  • Ascotoxin, Cyanein, DecuMbin
  • Brefeldin A, FroM EupenicilliuM brefeldianuM
  • NECTROLIDE
  • SYNERGISIDIN
  • 4h-cyclopent(f)oxacyclotridecin-4-one,1,6,7,8,9,11a-beta,12,13,14,14a-alpha-de
  • cahydro-1-beta-13-alpha-dihydroxy-6-beta-methyl-
  • cyanaein
  • DECUMBIN
  • GAMMA-4-DIHDYROXY-2-(6-HYDROXY-1-HEPTENYL)-4-CYCLOPENTANECROTONIC ACID LAMBDA-LACTONE
  • GAMMA,4-DIHYDROXY-2-[6-HYDROXY-1-HEPTENYL]-4-CYCLOPENTANECROTONIC ACID LAMBDA-LACTONE
  • (+)-BREFELDIN A, EUPENICILLIUM BREFELDIANUM
  • BREFELDIN A, EUPENICILLIUM BREFELDIANUM
  • BREFELDIN A
  • ASCOTOXIN
  • 1,6,7,8,9,11A,12,13,14,14A-DECAHYDRO-1,13-DIHYDROXY-6-METHYL-4H-CYCLOPENT[F]OXACYCLOTRIDECIN-4-ONE
  • Brefeldin A Cyanein Ascotoxin
  • 1,6,7,8,9,11AB,12,13,14,14AA-DECAHYDRO-1B,13A-DIHYDROXY-6B-METHYL-4H-CYCLOPENT(F)OXACYCLOTRIDECIN-4-ONE
  • BREFELDIN A, MOLECULAR BIOLOGY REAGENT
  • BREFELDIN A FROM PENICILLIUM BREFELDIANUM
  • Brefeldin A, >=99%
  • (1R,2E,6S,10E,13S)-1,13-Dihydroxy-6-methyl-6,7,8,9,12,13,14,14a-octahydro-1H-cyclopenta[f][1]o
  • Brefeldin A, natural
  • g-4-Dihdyroxy-2-(6-hydroxy-1-heptenyl)-4-cyclopentanecrotonic Acid, Lactone, BFA, Cyanein, Ascotoxin, Decumbin
  • 4H-Cyclopentfoxacyclotridecin-4-one, 1,6,7,8,9,11a,12,13,14,14a-decahydro-1,13-dihydroxy-6-methyl-, (1R,2E,6S,10E,11aS,13S,14aR)-
  • (+)-Brefeldin A, Ascotoxin, Cyanein, Decumbin, Nectrolide, Synergisidin
  • -4-Dihdyroxy-2-(6-hydroxy-1-heptenyl)-4-cyclopentanecrotonic Acid, -Lactone, BFA, Cyanein, Ascotoxin, Decumbin
  • Ascotoxin, BFA, Cyanein, Decumbin, γ,4-Dihydroxy-2-(6-hydroxy-1-heptenyl)-4-cyclopentanecrotonic acid λ-lactone
  • 4-Dihydroxy-2-(6-hydroxy-1-heptenyl)-4-cyclopentanecrotonic acid λ-lactone
  • BFA / Ascotoxin / Cyanein / Decumbin
  • BREFELDIN ARESEARCH GRADE
  • BrefeldinA,γ,4-Dihydroxy-2-(6-hydroxy-1-heptenyl)-4-cyclopentanecrotonic acid λ-lactone, Ascotoxin, BFA, Cyanein, Decumbin
  • Brefeldin A(BFA,Ascotoxin,Cyanein)
  • NSC 244390
  • NSC 89671
  • Brefeldin A(BFA)
  • Brefeldin A USP/EP/BP
  • Brefeldin A, 98%, from Eupenicillium brefeldianum
  • Brefeldin A, from Penicillium brefeldianum, ≥98% (HPLC)
  • CS-766
  • (+)-Brefeldin A, Eupenicillium brefeldianum - CAS 20350-15-6 - Calbiochem
  • (1R,2E,6S,10E,11aS,13S,14aR)-1,13-Dihydroxy-6-methyl-1,6,7,8,9,11a,12,13,14,14a-decahydro-4H-cyclopenta[f][1]oxacyclotridecin-4-one
  • Brefeldin A, Inhibitor of ADP-ribosylation factor
  • Brefeldin A, 10 mM in DMSO
  • (+)-Brefeldin A, Eupenicillium brefeldianum
  • csnpharm Brefeldin A
  • 2,2'-Azobis(2,4-dimethylvaleronitrile) (ADVN)
  • (+)-BREFELDIN A
  • BFA
  • Brefeldin
  • CYANEIN
  • 20350-15-6
  • 20350-16-6
  • C16H24O4
  • Antibiotics
  • Antibiotics A to Z
  • Antibiotics A-F
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