Antipain, dihydrochloride

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Antipain, dihydrochloride manufacturers

Antipain, dihydrochloride Basic information
Product Name:Antipain, dihydrochloride
Synonyms:ANTIPAIN (2HCL);ANTIPAIN HYDROCHLORIDE;[(S)-I-CARBOXY-2-PHENYLETHYL]-CARBAMOYL-L-ARG-L-VAL-ARGINAL;[(S)-1-CARBOXY-2-PHENETHYL]-CARBAMOYL-ARG-VAL-ARG-ALDEHYDE;(S)-[1-CARBOXY-2-PHENYL-ETHYL]-CARBAMOYL-ARG-VAL-ARG-ALDEHYDE;[(S)-1-CARBOXY-2-PHENYLETHYL]-CARBAMOYL-ARG-VAL-ARG-AL HYDROCHLORIDE;[(S)-1-CARBOXY-2-PHENYLETHYL]-CARBAMOYL-ARG-VAL-ARGINAL 2HCL;[(S)-1-CARBOXY-2-PHENYLETHYL]-CARBAMOYL-ARG-VAL-L-ARGININAL
CAS:37682-72-7
MF:C27H46Cl2N10O6
MW:677.62
EINECS:609-466-5
Product Categories:peptides;inhibitor;AN-AZ;Antineoplastic and Immunosuppressive Antibiotics;Broad Spectrum Inhibitors of Proteolytic Enzyme Classes;Cathepsin D;Cysteine Protease Inhibitor;A to C;Aldehydes;Antibiotics;Antibiotics by Application;Apoptosis Enzymes;Application Index;Bioactive Small Molecules;Biochemicals and Reagents;Building Blocks;C13-C60;Calpain;Calpain II;Calpain II Inhibitors;Carbonyl Compounds;Cathepsin B;Cathepsin/Granzyme Inhibitors &;Cell Biology;Cell Signaling and Neuroscience;Cell Signaling Enzymes;Chemical Structure Class;Chemical Synthesis;Coagulation Proteins and Reagents;Core Bioreagents;Substrates;Pepetides
Mol File:37682-72-7.mol
Antipain, dihydrochloride Structure
Antipain, dihydrochloride Chemical Properties
Melting point 209-217 °C
Boiling point 652.92°C (rough estimate)
density 1.2423 (rough estimate)
refractive index 1.6500 (estimate)
storage temp. -20°C
solubility H2O: 50 mg/mL
form White powder
color White
biological sourceStreptomyces sp.
Water Solubility 0.01M in water
Stability:Stable for 1 year from date of purchase as supplied. Solutions in distilled water may be stored at -20°C for up to 1 month.
InChIKeyYAHXZYICKJUJEO-BXLPLHKWSA-N
SMILESCl[H].Cl[H].[H]C(=O)C(CCCNC(N)=N)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)NC(Cc1ccccc1)C(O)=O)C(C)C
Safety Information
Safety Statements 22-24/25
WGK Germany 3
RTECS YV9350800
1-10
HS Code 2934999090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
Antipain, dihydrochloride Usage And Synthesis
DescriptionAntipain is a protease inhibitor originally isolated from actinomycetes. It inhibits thrombokinase, plasmin, trypsin, and papain in vitro (IC50s = 20, 93, 0.26, and 0.16 μg/ml, respectively). Antipain (6-600 μg/ml) inhibits the morphological transformation of and increases frequency of chromosomal aberrations in Syrian hamster embryo cells induced by N-methyl-N''-nitro-N-nitroso-guanidine (MNNG). In vivo, antipain (25-100 mg/kg) suppresses urethan-induced formation of cleft palates and cleft lips in mice.
UsesConcentrations for 50% inhibition (μg/ml): papain, 0.16trypsin, 0.26cathepsin A, 1.19cathepsin B, 0.59cathepsin D, 125plasmin, >93chymotrypsin and pepsin, >250It also has been reported to inhibit calpain I, (porcine) with Ki = 1.4 μM
UsesAntipain inhibits trypsin, papain, and catherpsins A and B (a reversible inhibitor of cysteine and serine proteases). It is used to evaluate the role of proteases in cell transformations. It is used to help identify new proteases.
General DescriptionAntipain is a protease inhibitor isolated from actinomycetes. It inhibits thrombokinase and blood coagulation.
Biochem/physiol ActionsReversible 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 of antipain can reduce the frequency of chemically induced transformation in BALB/c-/3T3 cells.
in vivo

The intact, cycling female mice received subcutaneous injections of Antipain dihydrochloride (3 mg) for 16 days, their uteri shows significant diminution in weight and total DNA when compared to untreated controls[4].
Antipain dihydrochloride (100 μg/g body wt; i.p.; at 12h intervals from 0 to 120 h or 240 to 360 h) shows inhibitory effect on Urethane-induced lung neoplasia in mice[5].

References[1] UMEZAWA H. Structures and activities of protease inhibitors of microbial origin.[J]. Methods in enzymology, 1976, 45: 678-695. DOI:10.1016/s0076-6879(76)45058-9
[2] T GOTOH. Proteolytic activity and recombinant protein production in virus-infected Sf-9 insect cell cultures supplemented with carboxyl and cysteine protease inhibitors.[J]. Journal of bioscience and bioengineering, 2001, 92 3: 248-255. DOI:10.1263/jbb.92.248
[3] K. HOCKENSMITH. Identification and characterization of a chymotrypsin-like serine protease from periodontal pathogen, Tannerella forsythia[J]. Microbial pathogenesis, 2016, 100: Pages 37-42. DOI:10.1016/j.micpath.2016.08.041
[4] AMIN N M. Proteinases in Naegleria Fowleri (strain NF3), a pathogenic amoeba: a preliminary study.[J]. Tropical biomedicine, 2004, 21 2: 57-60.
[5] YUJI MORIYASU  Yuko I. Use of protease inhibitors for detecting autophagy in plants.[J]. Methods in enzymology, 2008, 451: 557-580. DOI:10.1016/s0076-6879(08)03232-1
Antipain, dihydrochloride Preparation Products And Raw materials
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D-Amino acid oxidase α-Chymotrypsin Pectinase Acetyl coenzyme A sodium salt HEXOKINASE alpha-Amylase PROTEASE α-Amylase EC 2.6.1.2 Pepsin β-Amylase DISPASE Glucose oxidase N-1-naphthylethylenediamine hydrochloride Clindamycin hydrochloride Antipain hydrochloride dihydrate Antipain, dihydrochloride Antipain monohydrochloride dihydrate