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BATRACHOTOXIN

BATRACHOTOXIN Struktur
23509-16-2
CAS-Nr.
23509-16-2
Englisch Name:
BATRACHOTOXIN
Synonyma:
BTX;C13750;BATRACHOTOXIN;ISNYUQWBWALXEY-OMIQOYQYSA-N;Batrachotoxinin A, 20-(2,4-dimethyl-1H-pyrrole-3-carboxylate);1H-Pyrrole-3-carboxylicacid, 2,4-dimethyl-,(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-dodecahydro-9,12-dihydroxy-2,11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-;(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-Dodecahydro-9,12-dihydroxy-2-11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl2,4-dimethyl-1H-pyrrole-3-carboxylate;1H-Pyrrole-3-carboxylic acid, 2,4-dimethyl-, (1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-dodecahydro-9,12-dihydroxy-2,11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl ester
CBNumber:
CB01431991
Summenformel:
C31H42N2O6
Molgewicht:
538.67
MOL-Datei:
23509-16-2.mol

BATRACHOTOXIN Eigenschaften

alpha 
24584 -5 To -10°; 24300 -260° (c = 0.23 in methanol)
Siedepunkt:
614.87°C (rough estimate)
Dichte
1.1575 (rough estimate)
Brechungsindex
1.5800 (estimate)
storage temp. 
Store at -20°C
pka
7.45(at 25℃)
Aggregatzustand
Thin film.
Farbe
Noncrystal
CAS Datenbank
23509-16-2
EPA chemische Informationen
Betrachotoxinin A, 20-.alpha.-(2,4-dimethyl-1H-pyrrole-3-carboxylate) (23509-16-2)

Sicherheit

RIDADR  3172
HazardClass  6.1(b)
PackingGroup  III
Giftige Stoffe Daten 23509-16-2(Hazardous Substances Data)
Toxizit?t LD50 s.c. in mice: 2 mg/kg (Tokuyama)

BATRACHOTOXIN Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Noncrystal.

Hazard

Extremely toxic; deadly poison; neurotoxic; cardiotoxic activity; bara-chotoxin that blocks neuromuscular transmission; respiratory paralysis; death.

Biologische Aktivit?t

Potent neurotoxin that activates voltage-gated sodium channels. Shifts voltage-dependent activation to more negative potentials, inactivation is disabled and pore conductance and selectivity are altered (displays increased permeability for NH 4 + , K + and Cs + ions).

Sicherheitsprofil

A deadly poison byintraperitoneal, intravenous, and subcutaneous routes.When heated to decomposition it emits toxic fumes ofNOx.

Enzyminhibitor

This lipid-soluble neurotoxin (FW = 526.67 g/mol; CAS 23509-16-2; LD50 = ~2 μg/kg mouse body weight.), isolated from the skin of the Columbian poison-dart frog Phyllobates aurotaenis, enhances Na+ conductance, promoting opening of voltage-gated Na+ channels, inducing depolarization of the resting membrane potential. It does so by binding to the sodium channel, keeping the membrane permeable to sodium ions in an all-or-none manner. This results in hyperexcitability of excitable tissues, followed by convulsions, paralysis, and death in animals. The most common use of batrachotoxin is in darts for bloguns used in hunting by the Noanamá Chocó and Emberá Chocó Indians of western Colombia. Batrachotoxin has also been identified in the feathers of the passerine birds of New Guinea Pitohui dichrous, Pitohui kirhocephalus, and Ifrita kowaldi. The less toxic batrachotoxin A is the deesterified steroid.

BATRACHOTOXIN Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


BATRACHOTOXIN Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 12)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
RongNa Biotechnology Co.,Ltd
+86-86-13583358881 +8618560316533
Brad@rongnabiotech.com China 3378 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207
sales@molcore.com China 49734 58
GIHI CHEMICALS CO.,LIMITED
+86-571-86217390; +8618058761490
info@gihichemicals.com China 49954 58
DAYANG CHEM (HANGZHOU) CO.,LTD
+86-88938639 +86-17705817739
info@dycnchem.com China 53803 58
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037
3bsc@sina.com China 15838 69
Enzo Biochem Inc --
Enzoname@qq.com China 6174 58
Santa Cruz Biotechnology Inc --
scbt@scbt.com China 6594 58
Wenzhou Baichuan Biotechnology Co., Ltd --
CHINA 876 58

23509-16-2()Verwandte Suche:


  • Batrachotoxinin A, 20-(2,4-dimethyl-1H-pyrrole-3-carboxylate)
  • C13750
  • (1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-Dodecahydro-9,12-dihydroxy-2-11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl2,4-dimethyl-1H-pyrrole-3-carboxylate
  • BATRACHOTOXIN
  • 1H-Pyrrole-3-carboxylic acid, 2,4-dimethyl-, (1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-dodecahydro-9,12-dihydroxy-2,11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl ester
  • ISNYUQWBWALXEY-OMIQOYQYSA-N
  • 1H-Pyrrole-3-carboxylicacid, 2,4-dimethyl-,(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-dodecahydro-9,12-dihydroxy-2,11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-
  • BTX
  • 23509-16-2
  • Sodium channel
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