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N-Acetylputrescine hydrochloride, a member of the polyamine family, is a biologically significant compound derived from putrescine, which is essential for cell growth and division. It has been studied for its potential antineoplastic properties, as well as its role in various physiological and pathological processes, including inflammation, cardiovascular diseases, and neurodegeneration. Its potential use in drug delivery and as a biomarker for certain diseases makes it a compound of interest in scientific research and medicinal applications.

18233-70-0

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18233-70-0 Usage

Uses

Used in Anticancer Applications:
N-Acetylputrescine hydrochloride is used as an antineoplastic agent for its potential anti-cancer properties. It may play a role in modulating various oncological signaling pathways, exerting inhibitory effects on tumor growth and progression.
Used in Drug Delivery Systems:
N-Acetylputrescine hydrochloride is used in drug delivery systems to enhance its applications and efficacy in treating various diseases. It may be employed as a carrier for drug delivery, aiming to improve the delivery, bioavailability, and therapeutic outcomes of certain medications.
Used in Biomarker Research:
N-Acetylputrescine hydrochloride is used as a potential biomarker for certain diseases, given its involvement in physiological and pathological processes. Its presence or levels in biological samples may provide valuable information for disease diagnosis, prognosis, or monitoring treatment response.
Used in Research on Physiological and Pathological Processes:
N-Acetylputrescine hydrochloride is used in scientific research to study its role in various physiological and pathological processes, such as inflammation, cardiovascular diseases, and neurodegeneration. Understanding its mechanisms of action may contribute to the development of novel therapeutic strategies for these conditions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-Acetylputrescine hydrochloride is used as a compound of interest for the development of new drugs and therapies. Its biological significance and potential therapeutic uses make it a valuable target for research and drug discovery efforts.

Check Digit Verification of cas no

The CAS Registry Mumber 18233-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,3 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18233-70:
(7*1)+(6*8)+(5*2)+(4*3)+(3*3)+(2*7)+(1*0)=100
100 % 10 = 0
So 18233-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O.ClH/c1-6(9)8-5-3-2-4-7;/h2-5,7H2,1H3,(H,8,9);1H

18233-70-0 Well-known Company Product Price

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  • Aldrich

  • (A8784)  N-Acetylputrescinehydrochloride  ≥98% (TLC)

  • 18233-70-0

  • A8784-25MG

  • 601.38CNY

  • Detail
  • Aldrich

  • (A8784)  N-Acetylputrescinehydrochloride  ≥98% (TLC)

  • 18233-70-0

  • A8784-500MG

  • 4,864.86CNY

  • Detail

18233-70-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetylputrescine

1.2 Other means of identification

Product number -
Other names N-Acetylputrescine hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18233-70-0 SDS

18233-70-0Downstream Products

18233-70-0Relevant academic research and scientific papers

Methylglyoxal bis(guanylhydrazone) analogs: multifunctional inhibitors for polyamine enzymes

Nakashima, Kunio,Hibasami, Hiroshige,Tsukada, Tetsuya,Maekawa, Satoru

, p. 553 - 558 (1987)

Methylglyoxal bis(3-aminopropyl-amidinohydrazone)(MGBA), methylglyoxal bis(4-aminobutyl-amidinohydrazone)(MGBT), methylglyoxal bis(cyclohexyl-amidinohydrazone)(MGBC) and methylglyoxal bis(butyl-amidinohydrazone)(MGBB) were synthesized as potent competitiv

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