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PyBOP

PyBOP

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PyBOP, Catalog No: 31010
(Benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate, CAS: 128625-52-5, MW: 520.39, Formula: C18H28F6N6OP2
Catalog No: 31010
(Benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate, CAS: 128625-52-5, MW: 520.39, Formula: C18H28F6N6OP2
Description

Details

(Benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate
Additional Information

Additional Information

Catalog Number 31010
CAS 128625-52-5
M.W. 520.39
Formula C18H28F6N6OP2
IUPAC Name benzotriazol-1-yloxy(tripyrrolidin-1-yl)phosphanium hexafluorophosphate
Synonym (Benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate
Also Known As
  • benzotriazol-1-yloxy-tripyrrolidin-1-ylphosphanium hexafluorophosphate
  • benzotriazol-1-yloxy-tripyrrolidin-1-yl-phosphonium hexafluorophosphate
  • 1-benzotriazolyloxy-tri1-pyrrolidinylphosphonium hexafluorophosphate
  • benzotriazol-1-yloxy-tripyrrolidin-1-yl-phosphanium hexafluorophosphate
  • T5662404
  • (Benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate
  • 07549_FLUKA
  • PyBOP
  • 12805_FLUKA
  • 377848_ALDRICH
InChIKey VIAFLMPQBHAMLI-UHFFFAOYSA-N
InChI InChI=1S/C18H28N6OP.F6P/c1-2-10-18-17(9-1)19-20-24(18)25-26(21-11-3-4-12-21,22-13-5-6-14-22)23-15-7-8-16-23;1-7(2,3,4,5)6/h1-2,9-10H,3-8,11-16H2;/q+1;-1
SMILES C1CCN(C1)[P+](N2CCCC2)(N3CCCC3)ON4C5=CC=CC=C5N=N4.F[P-](F)(F)(F)(F)F
Cited Uses

Details

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15. Newcomb CJ et al, "Cell death versus cell survival instructed by supramolecular cohesion of nanostructures", Nature communications, 5() pp.3321 (2014).
16. Kumarasinghe IR et al, "Synthesis and Evaluation of Novel Cyclic Peptide Inhibitors of Lysine-Specific Demethylase 1", ACS medicinal chemistry letters, 5(1) pp.29-33 (2014 Jan 9).
17. Wojcik F et al, "Synthesis of homo- and heteromultivalent carbohydrate-functionalized oligo(amidoamines) using novel glyco-building blocks", Beilstein Journal of Organic Chemistry, 9() pp.2395-2403 ().
18. Flook AM et al, "Effects of Amino Acids on Melanoma Targeting and Clearance Properties of Tc-99m-Labeled Arg-X-Asp-Conjugated ?-Melanocyte Stimulating Hormone Peptides", Journal of medicinal chemistry, 56(21) pp.10.1021/jm4012356 (2013 Nov 14).
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22. Deuss PJ et al, "Parallel synthesis and splicing redirection activity of cell-penetrating peptide conjugate libraries of a PNA cargo †Electronic supplementary information (ESI) available: MALDI mass-spectroscopy data for peptides and PNA705 conjugates of LB1 and LB2. Amino acid sequences, purity, synthesis and conjugation yields of LB2. Examples of HPLC-graphs and MALDI mass-spectra for peptides and conjugates. Luciferase readout of LB1 crude and purified PNA705 conjugates and single data-point splice correction assay of LB2–PNA705 conjugates. See DOI: 10.1039/c3ob41659c Click here for additional data file.", Organic & Biomolecular Chemistry, 11(43) pp.7621-7630 (2013 Nov 21).
23. Nakagomi M et al, "A Novel Aromatic Carboxylic Acid Inactivates Luciferase by Acylation of an Enzymatically Active Regulatory Lysine Residue", PLoS ONE, 8(9) pp.e75445 ().
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25. Ward BP et al, "Peptide lipidation stabilizes structure to enhance biological function", Molecular Metabolism, 2(4) pp.468-479 ().
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