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11077-03-5

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11077-03-5 Usage

Safety Profile

A deadly poison by intraperitoneal, parenteral, subcutaneous, intravenous, intramuscular, and intratracheal routes. A skin and severe eye irritant. When heated to decomposition it emits toxic fumes of NOx.

Enzyme inhibitor

This structurally complex neurotoxin (FW = 2680.17 g/mol; CAS 11077- 03-5; Abbreviation: PLTX), from the Pacific soft coral Palythoa toxica, binds slowly, but with extreme affinity, to Na+/K+-exchanging ATPase, converting the latter into an open channel, allowing unhindered passage of potassium and sodium ions. Less than 1 pM palytoxin is required for rapid potassium ion outflow from erythrocytes, thereby dissipating its transmembrane electric potential. Palytoxin is lethal in mice, exhibiting an impressive LD50 of 15 ng/kg. The pore-forming action of palytoxin is not restricted to Na+/K+-ATPase, but is also observed with the colonic H+/K+-ATPase. This observation raises the likelihood that the toxin reacts at functionally and/or structurally similar manner with these pumps. PLTX brings about depolarization of the cellular membrane, disrupting intracellular calcium concentration ([Ca2+]i) and leading to smooth and cardiac muscle contraction, cytoskeletal dysregulation, and neurotransmitter release. Second only to maitotoxin as the most toxic natural product known, palytoxin evokes prompt onset of severe agina and asthma-like airway effects, followed quickly by tachycardia and death, often within minutes. SKF-96365 and Gd3+ are widely used to block store- operated and stretch-activated Ca2+ channels, respectively. SKF-96365 fails to affect the long-lasting phase elicited by PLTX, excluding the activation of the store-operated channels during this phase. In contrast, Gd3+ abolishes the long-lasting phase of the [Ca2+]i increase, suggesting a possible role for stretch-activated channels in PLTX action. While Gd3+ is also known to inhibit voltage-dependent Ca2+ conductance in neural cells, voltage-dependent Ca2+ blockade seems unlikely in muscle cells. Even at a level (100 μM) commonly used to investigate stretch-activated channels activity, Gd3+ does not affect the transient phase as Verapamil and La3+/Cd2+ does. In addition to the selective inhibitory action of Gd3+ on the long- lasting phase, Gd3+ also significantly reduces, albeit incompletely, the toxic effects of PLTX on skeletal muscle cells, suggesting a role for the stretch- activated channels in the chain of events culminating in death of cultured muscle cells. Palytoxin also binds to erythrocyte Band-3 protein (B3 or AE1), altering the anionic flux and seriously compromising not only CO2 (bicarbonate) transport, thereby also affecting hemoglobin oxygenation/deoxygenation. The stereocontrolled synthesis of palytoxin was heralded as one of the most complicated syntheses ever undertaken. (See Maitotoxin)

Check Digit Verification of cas no

The CAS Registry Mumber 11077-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,7 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 11077-03:
(7*1)+(6*1)+(5*0)+(4*7)+(3*7)+(2*0)+(1*3)=65
65 % 10 = 5
So 11077-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C129H223N3O54/c1-62(29-33-81(143)108(158)103(153)68(7)47-93-111(161)117(167)110(160)91(180-93)36-35-76(138)82(144)51-73-50-74-53-92(178-73)90(177-74)38-37-89-85(147)52-75(61-130)179-89)23-20-28-78(140)105(155)77(139)26-18-13-16-25-70(135)48-94-112(162)118(168)113(163)97(181-94)55-84(146)83(145)54-95-107(157)87(149)57-96(182-95)106(156)80(142)34-32-69(134)31-30-65(4)88(150)60-129(176)125(174)123(173)115(165)99(184-129)49-71(136)24-15-10-9-11-19-40-128-59-64(3)58-127(8,186-128)100(185-128)44-63(2)22-14-12-17-27-79(141)109(159)116(166)120(170)122(172)124-121(171)119(169)114(164)98(183-124)56-86(148)102(152)66(5)45-72(137)46-67(6)104(154)126(175)132-42-39-101(151)131-41-21-43-133/h13,16,18,20,23,25,30-31,35-36,39,42,45,63-65,67-100,102-125,133-150,152-174,176H,1,9-12,14-15,17,19,21-22,24,26-29,32-34,37-38,40-41,43-44,46-61,130H2,2-8H3,(H,131,151)(H,132,175)/b18-13+,23-20-,25-16-,31-30+,36-35-,42-39-,66-45+/t63-,64-,65-,67+,68+,69+,70+,71-,72-,73-,74+,75-,76+,77+,78+,79+,80+,81-,82+,83+,84+,85+,86-,87+,88-

11077-03-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name palytoxin

1.2 Other means of identification

Product number -
Other names PALYTOXIN (ACETAL)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:11077-03-5 SDS

11077-03-5Upstream product

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