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ANTIPAIN HYDROCHLORIDE DIHYDRATE

ANTIPAIN HYDROCHLORIDE DIHYDRATE Structure
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
Molecular Weight:
604.7
MOL File:
37691-11-5.mol
MSDS File:
SDS
Modify Date:
2023/5/15 10:43:29

ANTIPAIN HYDROCHLORIDE DIHYDRATE Properties

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

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
WGK Germany  3
RTECS  YV9350700
1-10

ANTIPAIN HYDROCHLORIDE DIHYDRATE price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 10791 Antipain >50000?U/mg 37691-11-5 5MG ₹11745.13 2022-06-14 Buy
Sigma-Aldrich(India) 10791 Antipain >50000?U/mg 37691-11-5 25MG ₹41849.45 2022-06-14 Buy
Product number Packaging Price Buy
10791 5MG ₹11745.13 Buy
10791 25MG ₹41849.45 Buy

ANTIPAIN HYDROCHLORIDE DIHYDRATE Chemical Properties,Uses,Production

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

Global( 73)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
Dideu Industries Group Limited +86-29-89586680 +86-15129568250 China 26165 58 Inquiry
Nextpeptide Inc +86-0571-81612335 +8613336028439 China 19915 58 Inquiry
Nanjing TGpeptide +86-13347807150 +86-13347807150 China 3279 58 Inquiry
Zhejiang Hangyu API Co., Ltd +8617531972939 China 2944 58 Inquiry
Shanghai Maclean Biochemical Technology Co., LTD 021-50706066 15221275939 China 29803 58 Inquiry
Baoji Didu Pharmaceutical and Chemical Co., Ltd 029-81148929 13186179623 China 10011 58 Inquiry
Zhejiang Jiekun Biotechnology Co., Ltd 0571-88211951 13735575465 China 4904 58 Inquiry
Chengdu Youngshe Chemical Co., Ltd. +86-17380623303 +86-17380623303 China 5948 58 Inquiry

37691-11-5(ANTIPAIN HYDROCHLORIDE DIHYDRATE)Related Search:

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