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ANTHRANILYL-HIV PROTEASE SUBSTRATE IV

Product Name
ANTHRANILYL-HIV PROTEASE SUBSTRATE IV
CAS No.
141223-69-0
Chemical Name
ANTHRANILYL-HIV PROTEASE SUBSTRATE IV
Synonyms
ANTHRANILYL-HIV PROTEASE SUBSTRATE;ANTHRANILYL-HIV PROTEASE SUBSTRATE IV;H-2-ABZ-THR-ILE-NLE-PHE(4-NO2)-GLN-ARG-NH2;anthranilyl-lys-ala-arg-val-nle-P-*nitro-phe-glu-;ANTHRANILYL-LYS-ALA-ARG-VAL-NLE-P-NITRO- PHE-GLU-AL;ABZ-LYS-ALA-ARG-VAL-NLE-P-NITRO-PHE-GLU-ALA-NLE-NH2;H-2-ABZ-LYS-ALA-ARG-VAL-NLE-PHE(4-NO2)-GLU-ALA-NLE-NH2;anthranilyl-Lys-Ala-Arg-Val-NLE-nitro-Phe-Glu-Ala-NLEamide;ANTHRANILYL-LYS-ALA-ARG-VAL-NLE-P-NITRO-PHE-GLU-ALA-NLE AMIDE;L-Norleucinamide,N2-(2-aminobenzoyl)-L-lysyl-L-alanyl-L-arginyl-L-valyl-L-norleucyl-4-nitro-L-phenylalanyl-L-α-glutamyl-L-alanyl-
CBNumber
CB3344846
Molecular Formula
C56H88N16O14
Formula Weight
1209.4
MOL File
141223-69-0.mol
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ANTHRANILYL-HIV PROTEASE SUBSTRATE IV Property

Density 
1.38±0.1 g/cm3(Predicted)
storage temp. 
−20°C
pka
4.43±0.10(Predicted)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
PEP0004309
Product name
ANTHRANILYL-LYS-ALA-ARG-VAL-NLE-P-NITRO-PHE-GLU-ALA-NLE AMIDE
Purity
95.00%
Packaging
1MG
Price
$910.17
Updated
2021/12/16

ANTHRANILYL-HIV PROTEASE SUBSTRATE IV Preparation Products And Raw materials

Raw materials

Preparation Products

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ANTHRANILYL-HIV PROTEASE SUBSTRATE IV Suppliers

China 17 Switzerland 1 United States 3 Global 21
SIGMA-RBI
Tel
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Fax
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Country
Switzerland
ProdList
6896
Advantage
91

141223-69-0, ANTHRANILYL-HIV PROTEASE SUBSTRATE IVRelated Search:

2-amino-n-butyl-benzamide HIV PROTEASE SUBSTRATE IV N-Methyl-4-nitrophenethylamine hydrochloride ANTHRANILYL-HIV PROTEASE SUBSTRATE IV Benzenepropanamine, 4-amino- (9CI) N-ACETYL-2-(4-NITROPHENYL)ETHYLAMINE N1-(SEC-BUTYL)-2-AMINOBENZAMIDE 3-(4-NITROPHENYL)PROPAN-1-AMINE

  • ANTHRANILYL-HIV PROTEASE SUBSTRATE IV
  • ANTHRANILYL-LYS-ALA-ARG-VAL-NLE-P-NITRO-PHE-GLU-ALA-NLE AMIDE
  • H-2-ABZ-LYS-ALA-ARG-VAL-NLE-PHE(4-NO2)-GLU-ALA-NLE-NH2
  • H-2-ABZ-THR-ILE-NLE-PHE(4-NO2)-GLN-ARG-NH2
  • anthranilyl-lys-ala-arg-val-nle-P-*nitro-phe-glu-
  • ANTHRANILYL-LYS-ALA-ARG-VAL-NLE-P-NITRO- PHE-GLU-AL
  • anthranilyl-Lys-Ala-Arg-Val-NLE-nitro-Phe-Glu-Ala-NLEamide
  • ABZ-LYS-ALA-ARG-VAL-NLE-P-NITRO-PHE-GLU-ALA-NLE-NH2
  • ANTHRANILYL-HIV PROTEASE SUBSTRATE
  • L-Norleucinamide,N2-(2-aminobenzoyl)-L-lysyl-L-alanyl-L-arginyl-L-valyl-L-norleucyl-4-nitro-L-phenylalanyl-L-α-glutamyl-L-alanyl-
  • L-Norleucinamide, N2-(2-aminobenzoyl)-L-lysyl-L-alanyl-L-arginyl-L-valyl-L-norleucyl-4-nitro-L-phenylalanyl-L-α-glutamyl-L-alanyl- (9CI)
  • 141223-69-0
  • C56H88N16O14
  • Activity
  • BioChemical
  • Biochemicals and Reagents
  • HIV Protease
  • Substrates by Enzyme
  • Fluorogenic
  • Enzyme Substrates
  • Enzymes, Inhibitors, and Substrates
  • Activity
  • Enzyme Substrates
  • Fluorogenic