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ANTIPAIN HYDROCHLORIDE DIHYDRATE

Product Name
ANTIPAIN HYDROCHLORIDE DIHYDRATE
CAS No.
37691-11-5
Chemical Name
ANTIPAIN HYDROCHLORIDE DIHYDRATE
Synonyms
Aids006469;Aids-006469;PHE-ARG-VAL-ARG-CHO;ANTIPAIN ~10000 U/MG;Phe-co-Arg-Val-L-Arg-h;Antipain research grade;ANTIPAIN HYDROCHLORIDE DIHYDRATE;ANTIPAIN HYDROCHLORIDE DIHYDRATE USP/EP/BP;4-((aminoiminomethyl)amino)-1-formylbutyl)-;Nα-[Nα-[[(1-Carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl]-N-(1-formyl-4-guanidinobutyl)-L-valinamide
CBNumber
CB4279464
Molecular Formula
C27H44N10O6
Formula Weight
604.7
MOL File
37691-11-5.mol
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ANTIPAIN HYDROCHLORIDE DIHYDRATE Property

Density 
1.38
storage temp. 
−20°C
pka
3.84±0.10(Predicted)
BRN 
6837629
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Safety

WGK Germany 
3
RTECS 
YV9350700
F 
1-10
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P330Rinse mouth.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
10791
Product name
Antipain
Purity
>50000U/mg
Packaging
5mg
Price
$126
Updated
2024/03/01
Sigma-Aldrich
Product number
10791
Product name
Antipain
Purity
>50000U/mg
Packaging
25mg
Price
$269.4
Updated
2024/03/01
TRC
Product number
A697518
Product name
Antipain
Packaging
1mg
Price
$120
Updated
2021/12/16
AK Scientific
Product number
L979
Product name
Antipain
Packaging
5mg
Price
$347
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA39747
Product name
Antipain
Packaging
10mg
Price
$400
Updated
2021/12/16
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ANTIPAIN HYDROCHLORIDE DIHYDRATE Chemical Properties,Usage,Production

Uses

Antipain is a reversible inhibitor of Ser and Cys proteases.

General Description

Chemical structure: peptide

Biochem/physiol Actions

Reversible inhibitor of serine/cysteine proteases and some trypsin-like serine proteases. Its action resembles leupeptin; however, its plasmin inhibition is less and its cathepsin A inhibition is more than that observed with leupeptin. Chronic administration can reduce the frequency of chemically induced transformation in BALB/c-/3T3 cells.

ANTIPAIN HYDROCHLORIDE DIHYDRATE Preparation Products And Raw materials

Raw materials

Preparation Products

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ANTIPAIN HYDROCHLORIDE DIHYDRATE Suppliers

China 54 Europe 2 Germany 2 India 1 Japan 1 Switzerland 1 United Kingdom 1 United States 12 Global 74
Carbosynth
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
Advantage
58
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View Lastest Price from ANTIPAIN HYDROCHLORIDE DIHYDRATE manufacturers

Dideu Industries Group Limited
Product
ANTIPAIN HYDROCHLORIDE DIHYDRATE 37691-11-5
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons Min
Release date
2021-07-19

37691-11-5, ANTIPAIN HYDROCHLORIDE DIHYDRATERelated Search:

ANTIPAIN MONOHYDROCHLORIDE DIHYDRATE ANTIPAIN HYDROCHLORIDE DIHYDRATE ANTIPAIN, DIHYDROCHLORIDE

  • N2-[[(1-Carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-valinamide
  • PHE-ARG-VAL-ARG-CHO
  • Antipain research grade
  • 4-((aminoiminomethyl)amino)-1-formylbutyl)-
  • ANTIPAIN HYDROCHLORIDE DIHYDRATE
  • N2-[[(1-carboxyphenethyl)amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-valinamide
  • ANTIPAIN ~10000 U/MG
  • Nα-[N2-[[(1-Carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl]-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-valinamide
  • Nα-[Nα-[[(1-Carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl]-N-(1-formyl-4-guanidinobutyl)-L-valinamide
  • Aids006469
  • Aids-006469
  • L-Valinamide, N(sup 2)-(((1-carboxy-2-phenylethyl)amino)carbonyl)-L-arginyl-N-(4-((aminoiminomethyl)amino)-1-formylbutyl)-
  • Phe-co-Arg-Val-L-Arg-h
  • L-Valinamide, N2-[[(1-carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-
  • ANTIPAIN HYDROCHLORIDE DIHYDRATE USP/EP/BP
  • 37691-11-5
  • C27H44N10O6HCl
  • C27H49ClN10O8
  • C27H44N10O6
  • A - K
  • Aldehydes
  • Antibacterial
  • Antibiotics A to Z
  • Antibiotics
  • Antibiotics A-F
  • Antibiotics by Application
  • Antineoplastic and Immunosuppressive Antibiotics
  • Building Blocks
  • C13-C60
  • Carbonyl Compounds
  • Chemical Structure Class
  • Chemical Synthesis
  • Inhibits an Enzyme
  • Mechanism of Action
  • Organic Building Blocks
  • Peptides
  • Spectrum of Activity
  • Pepetides