Calcitonin (salmon) xAcetate

CAS: 47931-85-1

Ref. TR-C144555

Información del producto

• Nombre: Calcitonin (salmon) xAcetate
• Sinónimos: 1,2-Dithia-5,8,11,14,17,20-hexaazacyclotricosane Cyclic Peptide Deriv., 1: PN: US20130183385 SEQID: 1 Claimed Protein, 1: PN: WO2013067357 SEQID: 1 Claimed Protein, Calciben, Calcimar, Calcitonin (salmon reduced) Cyclic (1?7)-Disulfide, Calcitonin (Salmon reduced) Cyclic (1?7)-Disulfide, Calsyn, Calsynar, Catonin, Karil, Miacalcic, Miacalcin, Miadenil, Prontocalcin, Rulicalcin, SMC 021 A/C, Salcatonin, Salmon Thyrocalcitonin, Salmon calcitonin, Salmon calcitonin I, Salmon calcitonin-(1-32), Salmotonin, Stalcin, Tonocalcin, L-Prolinamide, L-Cysteinyl-L-Seryl-L-Asparaginyl-L-Leucyl-L-Seryl-L-Threonyl-L-Cysteinyl-L-Valyl-L-Leucylglycyl-L-Lysyl-L-Leucyl-L-Seryl-L-Glutaminyl-L-a-Glutamyl-L-Lucyl-L-Histidyl-L-Lysyl-L-Leucyl-L-Glutaminyl-L-Threonyl-L-Tyrosyl-L-Prolyl-L-Arginyl-L-Threonyl-L-Asparaginyl-L-Threonylglycyl-L-Serylglycyl-L-Threonyl Cyclic (1?7)-disulfide, Calcitonin (salmon I), Thyrocalcitonin Salmon, H-Cys-Ser-Asn-Leu-Ser-Thr-Cys-Val-Leu-Gly-Lys-Leu-Ser-Gln-Glu-Leu-His-Lys-Leu-Gln-Thr-Tyr-Pro-Arg-Thr-Asn-Thr-Gly-Ser-Gly-Thr-Pro-NH2 (Disulfide bond), Thyrocalcitonin, Salcitonin, Salmon Calcitonin acetate, Salmon, Calcitonin salmon Acetate, Calcitonin (Lachs), Calcitonin (salmon reduced) cyclic (1→7)-disulfide, Calcitonina (Salmon), Calcitonine (Saumon), L-Prolinamide, L-cysteinyl-L-seryl-L-asparaginyl-L-leucyl-L-seryl-L-threonyl-L-cysteinyl-L-valyl-L-leucylglycyl-L-lysyl-L-leucyl-L-seryl-L-glutaminyl-L-α-glutamyl-L-leucyl-L-histidyl-L-lysyl-L-leucyl-L-glutaminyl-L-threonyl-L-tyrosyl-L-prolyl-L-arginyl-L-threonyl-L-asparaginyl-L-threonylglycyl-L-serylglycyl-L-threonyl-, cyclic (1→7)-disulfide

Descripción

Applications Calcitonin (salmon), is a 32-amino acid linear polypeptide hormone that is produced in thyroid in humans. It acts to reduce blood calcium (Ca2+), opposing the effects of parathyroid hormone (PTH).
References Boron, WF. et al.: Med. Phys., A Cellular and Molecular Approach (2004); Andreotti, G. et al.: J. Bio. Chem., 281, 24193 (2006);

• Marca: TRC

Propiedades químicas

• Peso molecular: 3431.856005
• Fórmula: C₁₄₅H₂₄₀N₄₄O₄₈S₂·x(CH₃CO₂H)
• Color/Forma: Neat
• InChI: InChI=1S/C145H240N44O48S2.2C2H4O2/c1-65(2)45-86(175-139(232)110(70(11)12)183-136(229)99-63-239-238-62-79(148)117(210)178-96(59-191)134(227)174-92(52-104(151)202)131(224)172-90(49-69(9)10)129(222)180-98(61-193)135(228)187-114(74(16)197)142(235)181-99)118(211)158-55-106(204)162-80(25-18-20-40-146)120(213)169-89(48-68(7)8)128(221)179-97(60-192)133(226)167-83(34-37-102(149)200)122(215)165-85(36-39-109(207)208)123(216)171-88(47-67(5)6)127(220)173-91(51-77-54-156-64-161-77)130(223)164-81(26-19-21-41-147)121(214)170-87(46-66(3)4)126(219)166-84(35-38-103(150)201)125(218)186-113(73(15)196)141(234)177-94(50-76-30-32-78(199)33-31-76)143(236)189-44-24-29-101(189)137(230)168-82(27-22-42-157-145(154)155)124(217)185-112(72(14)195)140(233)176-93(53-105(152)203)132(225)184-111(71(13)194)138(231)160-56-107(205)163-95(58-190)119(212)159-57-108(206)182-115(75(17)198)144(237)188-43-23-28-100(188)116(153)209;2*1-2(3)4/h30-33,54,64-75,79-101,110-115,190-199H,18-29,34-53,55-63,146-148H2,1-17H3,(H2,149,200)(H2,150,201)(H2,151,202)(H2,152,203)(H2,153,209)(H,156,161)(H,158,211)(H,159,212)(H,160,231)(H,162,204)(H,163,205)(H,164,223)(H,165,215)(H,166,219)(H,167,226)(H,168,230)(H,169,213)(H,170,214)(H,171,216)(H,172,224)(H,173,220)(H,174,227)(H,175,232)(H,176,233)(H,177,234)(H,178,210)(H,179,221)(H,180,222)(H,181,235)(H,182,206)(H,183,229)(H,184,225)(H,185,217)(H,186,218)(H,187,228)(H,207,208)(H4,154,155,157);2*1H3,(H,3,4)/t71-,72-,73-,74-,75-,79+,80+,81+,82+,83+,84+,85+,86+,87+,88+,89+,90+,91+,92+,93+,94+,95+,96+,97+,98+,99+,100+,101+,110+,111+,112+,113+,114+,115+;;/m1../s1