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1-Piperazineacetic acid, 4-(phenylmethyl)-, hydrazide is an organic compound with the molecular formula C12H16N4O. It is a derivative of piperazineacetic acid, featuring a phenylmethyl group at the 4-position and a hydrazide group. 1-Piperazineaceticacid, 4-(phenylmethyl)-, hydrazide is known for its potential applications in the pharmaceutical industry due to its unique structural properties and reactivity.

24632-70-0

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24632-70-0 Usage

Uses

Used in Pharmaceutical Industry:
1-Piperazineacetic acid, 4-(phenylmethyl)-, hydrazide is used as an intermediate in the synthesis of PAC-1 (P132000), which is a caspase 3 activator. Caspase 3 is a crucial enzyme involved in the execution phase of apoptosis or programmed cell death. By activating caspase 3, PAC-1 can potentially induce apoptosis in cells, making it a valuable compound for the development of therapeutic agents targeting various diseases, including cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 24632-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24632-70:
(7*2)+(6*4)+(5*6)+(4*3)+(3*2)+(2*7)+(1*0)=100
100 % 10 = 0
So 24632-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2O2/c16-13(17)11-15-8-6-14(7-9-15)10-12-4-2-1-3-5-12/h1-5H,6-11H2,(H,16,17)

24632-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-benzylpiperazin-1-yl)acetohydrazide

1.2 Other means of identification

Product number -
Other names (4-benzyl-piperazin-1-yl)-acetic acid hydrazide

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:24632-70-0 SDS

24632-70-0Relevant articles and documents

Synthesis and initial in vitro biological evaluation of two new zinc-chelating compounds: Comparison with TPEN and PAC-1

?strand, O. Alexander H.,Aziz, Gulzeb,Ali, Sidra Farzand,Paulsen, Ragnhild E.,Hansen, Trond Vidar,Rongved, P?l

, p. 5175 - 5181 (2013/09/02)

The lipophilic, cell-penetrating zinc chelator N,N,N′,N′,- tetrakis(2-pyridylmethyl) ethylenediamine (TPEN, 1) and the zinc chelating procaspase-activating compound PAC-1 (2) both have been reported to induce apoptosis in various cell types. The relations

Synthesis, molecular modeling and evaluation of novel N′-2-(4- benzylpiperidin-/piperazin-1-yl)acylhydrazone derivatives as dual inhibitors for cholinesterases and Aβ aggregation

Oezturan Oezer, Eda,Unsal Tan, Oya,Ozadali, Keriman,Kuecuekkilinc, Tuba,Balkan, Ayla,Ucar, Guelberk

supporting information, p. 440 - 443 (2013/02/23)

To develop new drugs for treatment of Alzheimer's disease, a group of N′-2-(4-Benzylpiperidin-/piperazin-1-yl)acylhydrazones was designed, synthesized and tested for their ability to inhibit acetylcholinesterase, butyrylcholinesterase and aggregation of a

DESIGN, SYNTHESIS AND EVALUATION OF PROCASPASE ACTIVATING COMPOUNDS AS PERSONALIZED ANTI-CANCER DRUGS

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Page/Page column 31, (2010/08/18)

Compositions and methods are disclosed in embodiments relating to induction of cell death such as in cancer cells. Compounds and related methods for synthesis and use thereof, including the use of compounds in therapy for the treatment of cancer and selective induction of apoptosis in cells are disclosed. Compounds are disclosed that have lower neurotoxicity effects than other compounds.

COMPOSITIONS AND METHODS INCLUDING CELL DEATH INDUCERS AND PROCASPASE ACTIVATION

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Page/Page column 68, (2008/12/08)

Compositions and methods are disclosed in embodiments relating to induction of cell death such as in cancer cells. Compounds and related methods for synthesis and use thereof, including the use of compounds in therapy for the treatment of cancer and selective induction of apoptosis in cells are disclosed. Compounds are disclosed in connection with modification of procaspases such as procaspase-3. In embodiments, compositions are capable of activation of procaspase-3.

SELECTIVE APOPTOTIC INDUCTION IN CANCER CELLS INCLUDING ACTIVATION OF PROCASPASE-3

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Page/Page column 32-33, (2008/06/13)

Compounds and related methods for synthesis, and the use of compounds in therapy for the treatment of cancer and selective induction of apoptosis in cells are disclosed. Compounds are disclosed in connection with modification of procaspases such as procaspase-3, and particular embodiments are capable of direct activation of procaspase-3 and procaspase-7 to the effector forms of caspase-3 and caspase-7. Procaspase-3 levels can vary among cancer cell types; several types have relatively high levels and can have increased susceptibility to chemotherapy by compounds and methods herein. Therapeutic applications are relevant for a variety of cancer conditions and cell types, e.g. breast, lung, brain, colon, renal, adrenal, melanoma, and others.

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