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(Acyl)polyamines 
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2,4-(OH)₂-PhAc 
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2,5-(OH)₂-Bz 
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4-OH-Bz 
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4-OH-IndAc 
-- 4-OH-IndAc3 
-- 4-OH-IndAc3(Me₂)4(Me)3(NMe)⁺ 
-- 4-OH-IndAc3(Me₂)4(Me)3Arg⁺ 
-- 4-OH-IndAc3(Me₂)4(Me₂)3Arg²⁺ 
-- 4-OH-IndAc3(Me₂)4(NMe)⁺ 
-- 4-OH-IndAc3(Me₂)4(NMe₂)⁺ 
-- 4-OH-IndAc3(OH)3 
-- 4-OH-IndAc3(OH)3(OH)33 
-- 4-OH-IndAc3(OH)3(OH)34 
-- 4-OH-IndAc3(OH)3(OH)343 
-- 4-OH-IndAc3(OH)3(OH)35(NMe₃)⁺ 
-- 4-OH-IndAc3(OH)3(OH)43 
-- 4-OH-IndAc3(OH)33 
-- 4-OH-IndAc3(OH)333 
-- 4-OH-IndAc3(OH)3334Gu 
-- 4-OH-IndAc3(OH)334 
-- 4-OH-IndAc3(OH)3343 
-- 4-OH-IndAc3(OH)3343Ac 
-- 4-OH-IndAc3(OH)334Gu 
-- 4-OH-IndAc3(OH)335 
-- 4-OH-IndAc3(OH)335(NMe) 
-- 4-OH-IndAc3(OH)335(NMe₂) 
-- 4-OH-IndAc3(OH)335(NMe₃)⁺ 
-- 4-OH-IndAc3(OH)34 
-- 4-OH-IndAc3(OH)343 
-- 4-OH-IndAc3(OH)34Gu 
-- 4-OH-IndAc3(OH)35(NMe₃)⁺ 
-- 4-OH-IndAc3(OH)4 
-- 4-OH-IndAc3(OH)43 
-- 4-OH-IndAc3333 
-- 4-OH-IndAc33334Gu 
-- 4-OH-IndAc3334 
-- 4-OH-IndAc33343 
-- 4-OH-IndAc3334Gu 
-- 4-OH-IndAc3335(NMe₃)⁺ 
-- 4-OH-IndAc334 
-- 4-OH-IndAc3343 
-- 4-OH-IndAc334Gu 
-- 4-OH-IndAc335(NMe₃)⁺ 
-- 4-OH-IndAc34 
-- 4-OH-IndAc343 
-- 4-OH-IndAc3433 
-- 4-OH-IndAc35 
-- 4-OH-IndAc353 
-- 4-OH-IndAc4(OH)3 
-- 4-OH-IndAc4(OH)3(OH)33 
-- 4-OH-IndAc4(OH)33 
-- 4-OH-IndAc4(OH)333 
-- 4-OH-IndAc4(OH)3333 
-- 4-OH-IndAc43 
-- 4-OH-IndAc433 
-- 4-OH-IndAc4333 
-- 4-OH-IndAc4Gu 
-- 4-OH-IndAc5 
-- 4-OH-IndAc5(NMe₃)⁺ 
-- 4-OH-IndAc5(OH)33 
-- 4-OH-IndAc5(OH)3333 
-- 4-OH-IndAc53 
-- 4-OH-IndAc533 
-- 4-OH-IndAc5333 
-- 4-OH-IndAcAsn3(Me)4(Me)3Arg 
-- 4-OH-IndAcAsn3(Me)43 
-- 4-OH-IndAcAsn333 
-- 4-OH-IndAcAsn34 
-- 4-OH-IndAcAsn343 
-- 4-OH-IndAcAsn34ßAla3 
-- 4-OH-IndAcAsn34ßAla4 
-- 4-OH-IndAcAsn353 
-- 4-OH-IndAcAsn4 
-- 4-OH-IndAcAsn4(Me)3 
-- 4-OH-IndAcAsn43 
-- 4-OH-IndAcAsn433 
-- 4-OH-IndAcAsn433Arg 
-- 4-OH-IndAcAsn433Lys 
-- 4-OH-IndAcAsn433ßAla4 
-- 4-OH-IndAcAsn433ßAla4ßAla4 
-- 4-OH-IndAcAsn43Arg 
-- 4-OH-IndAcAsn43Lys 
-- 4-OH-IndAcAsn43ßAla4 
-- 4-OH-IndAcAsn4Lys(Me₂)3Arg⁺ 
-- 4-OH-IndAcAsn4ßAla3Arg 
-- 4-OH-IndAcAsn4ßAla3ßAla4ßAla4 
-- 4-OH-IndAcAsn4ßAla3ßAla4ßAla4ßAla4 
-- 4-OH-IndAcAsn4ßAla4 
-- 4-OH-IndAcAsn4ßAla43 
-- 4-OH-IndAcAsn4ßAla4Arg 
-- 4-OH-IndAcAsn4ßAla4ßAla4 
-- 4-OH-IndAcAsn5 
-- 4-OH-IndAcAsn53 
-- 4-OH-IndAcAsn533 
-- 4-OH-IndAcAsn533Arg 
-- 4-OH-IndAcAsn5Gly4 
-- 4-OH-IndAcAsn5Gly4ßAla4 
-- 4-OH-IndAcAsn5Gly4ßAla4ßAla4 
-- 4-OH-IndAcAsn5Gly4ßAla4ßAla4ßAla4 
-- 4-OH-IndAcAsn5Lys(Me)3Arg 
-- 4-OH-IndAcAsn5Lys(Me₂)3Arg⁺ 
-- 4-OH-IndAcAsn5ßAla3 
-- 4-OH-IndAcAsn5ßAla3Arg 
-- 4-OH-IndAcAsn5ßAla3ßAla4ßAla4 
-- 4-OH-IndAcAsn5ßAla3ßAla4ßAla4ßAla4 
-- 4-OH-IndAcAsn5ßAla4 
-- 4-OH-IndAcAsn5ßAla43 
-- 4-OH-IndAcAsn5ßAla43Arg 
-- 4-OH-IndAcAsn5ßAla43ßAla4 
-- 4-OH-IndAcAsn5ßAla43ßAla4ßAla4 
-- 4-OH-IndAcAsn5ßAla4Arg 
-- 4-OH-IndAcAsn5ßAla4OrnArg 
-- 4-OH-IndAcAsn5ßAla4ßAla4 
-- 4-OH-IndAcAsn5ßAla4ßAla4ßAla4 
-- 4-OH-IndAcAsn5ßAla4ßAla4ßAla4ßAla4 
-- 4-OH-IndAcLysMe53Arg 
-- 4-OH-IndAcLysMe₂5(Me)3Arg 
-- 4-OH-IndAcOrnAsn5ßAla4ßAla4 
-- 4-OH-IndAcOrnAsn5ßAla4ßAla4ßAla4 
-- 4-OH-IndAcßAla343 
-- 4-OH-IndAcßAla353 
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4-OH-PhAc 
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4-OH-PhLac 
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Ac 
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Bz 
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IndAc 
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IndLac 
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OH-OMe-Bz 
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PhAc 
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Phe 
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PhLac 
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Prop 
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Trp 
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Tyr 
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Unknown acylpolyamines 
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Free polyamines (PA) 
Small compounds 
Analytical tools 
Contact us   4-OH-IndAc3(Me₂)4(NMe)⁺ 
General Description Name Value Level S-3 / C-1 Discovered 2020 / P. bistriata Synonym — Molecular formula C₂₀H₃₃N₄O₂⁺ CAS — SMILES O=C(NCCC[N+](C)(C)CCCCNC)CC1=CNC2=C1C(O)=CC=C2InChI InChI=1S/C20H32N4O2/c1-21-10-4-5-12-24(2,3)13-7-11-22-19(26)14-16-15-23-17-8-6-9-18(25)20(16)17/h6,8-9,15,21,23H,4-5,7,10-14H2,1-3H3,(H-,22,25,26)/p+1Precursor 1 M⁺ 361.25980 Precursor 2 [M+H]²⁺ 181.13354 Precursor 3 HDX 4 Precursor HDX M(D₄)⁺ 365.28491 Precursor HDX 2 [M(D₄)+D]²⁺ 183.64923 Precursor HDX 3 Rt 7.31 Rt HDX 5.89 
Calculated MS/MS fragments # a b c ta z y tz 1 231.11280 213.10224 214.08626 276.17065 86.09643 69.06988 131.15428 2 330.21760 312.20704 313.19105 361.25980 171.18558 155.16685 188.21212 
Additional MS/MS fragments m/z Annotation 146.06004 a’ 174.05495 a0 
Recorded MS/MS spectra pdf Precursor Co-eluting Spider Source Author Data 361.25980 P. bistriata Prof. Dr. Wagner Ferreira dos Santos, BRA Y. M. Forster Data HDX P. bistriata Prof. Dr. Wagner Ferreira dos Santos, BRA Y. M. Forster 
References Title Reference Spider Name Content Link Elucidation of the structure and synthesis of neuroprotective low molecular mass components of the Parawixia bistriata spider venom Y. M. Forster, J. L. Green, A. Khatiwada, J. L. Liberato, P. A. Narayana Reddy, J. M. Salvino, S. Bienz, L. Bigler, W. Ferreira dos Santos, A. C. K. Fontana, ACS Chem Neurosci., 2020 P. bistriata ESI-MS/MS Link 
Spider species Spider species Family Discovered Parawixia bistriata Araneidae 2020 / Y. M. Forster