CAS 2900996-95-2

Formula: C103H169N43O27

InChI: InChI=1S/C103H169N43O27/c1-4-51(2)77(93(171)145-78(52(3)148)94(172)138-67(79(105)157)47-75(153)154)144-87(165)66(21-12-42-129-103(120)121)134-84(162)62(17-8-38-125-99(112)113)135-89(167)69(45-54-25-31-57(150)32-26-54)140-85(163)64(19-10-40-127-101(116)117)133-82(160)61(16-7-37-124-98(110)111)131-81(159)60(15-6-36-123-97(108)109)132-83(161)63(18-9-39-126-100(114)115)137-91(169)71(48-76(155)156)141-90(168)70(46-55-27-33-58(151)34-28-55)142-92(170)73-22-13-43-146(73)95(173)72(50-147)143-86(164)65(20-11-41-128-102(118)119)136-88(166)68(44-53-23-29-56(149)30-24-53)139-80(158)59(130-74(152)49-104)14-5-35-122-96(106)107/h23-34,51-52,59-73,77-78,147-151H,4-22,35-50,104H2,1-3H3,(H2,105,157)(H,130,152)(H,131,159)(H,132,161)(H,133,160)(H,134,162)(H,135,167)(H,136,166)(H,137,169)(H,138,172)(H,139,158)(H,140,163)(H,141,168)(H,142,170)(H,143,164)(H,144,165)(H,145,171)(H,153,154)(H,155,156)(H4,106,107,122)(H4,108,109,123)(H4,110,111,124)(H4,112,113,125)(H4,114,115,126)(H4,116,117,127)(H4,118,119,128)(H4,120,121,129)/t51-,52+,59-,60-,61-,62-,63-,64-,65-,66-,67-,68-,69-,70-,71-,72-,73-,77-,78-/m0/s1

InChI key: ZGMXUPVWRQVUKG-ONTXGEKHSA-N

SMILES: CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(=O)O)C(=O)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@@H]3CCCN3C(=O)[C@H](CO)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC4=CC=C(C=C4)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN

GeX-2

CAS: 2900996-95-2

GeX-2 is a truncated analogue of αO-conotoxin. It has the ability to activate GABAB receptors and inhibit α9α10nAChR as well as CaV2.2 channels. Additionally, GeX-2 is effective in alleviating pain in a rat model of chronic constriction injury.

Formula: C₁₀₃H₁₆₉N₄₃O₂₇

Colore e forma: Solid

Peso molecolare: 2441.72

Ref: TM-TP3132