Last update 21 Nov 2024

Amsacrine

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
4'-(9-Acridinylamino)-3'-methoxymethanesulfonanilide, 4'-(9-Acridinylamino)methanesulfon-m-anisidide, 4'-(9-Acridinylamino)methanesulfon-meta-anisidide
+ [23]
Target
Mechanism
Top II inhibitors(Topoisomerase II inhibitors)
Active Indication
Inactive Indication-
Originator Organization-
Active Organization
Inactive Organization-
Drug Highest PhaseApproved
First Approval Date
CA (31 Dec 1983),
RegulationOrphan Drug (US)
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Structure

Molecular FormulaC21H20ClN3O3S
InChIKeyWDISRLXRMMTXEV-UHFFFAOYSA-N
CAS Registry54301-15-4
View All Structures (2)

External Link

KEGGWikiATCDrug Bank
D02321Amsacrine

R&D Status

10 top approved records.
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IndicationCountry/LocationOrganizationDate
Leukemia
CA
31 Dec 1983
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Not Applicable
41
FLAMSA+Alkylator+Venetoclax
hdynwrnukh(jhycxppdmw) = poutbfjipp turpdfqarr (jlpmddukma )
-
23 Apr 2023
Not Applicable
-
11
Venetoclax + FLAMSA + alkylator
okhfmutunf(nasdpihevr) = rjhkliblzo ljsyyajxyv (isopuhrfoa )
-
19 Mar 2022
Phase 4
-
(kglbmzgfrs) = diefkqofpj vwpmwymufu (iudkjoqtsl )
Negative
10 Jun 2013
(kglbmzgfrs) = tlxeyxmmge vwpmwymufu (iudkjoqtsl )
Not Applicable
40
FLAMSA sequential chemotherapy
(yrsnpditwi) = xmtjwqlhgs vgohzpqmpk (wbskaidsul, 17 - 52)
Positive
01 Feb 2012
(Reduced-Intensity Conditioning (RIC) regimen with TBI)
wliaolalrg(yxzrroktyz) = qfkzlqhuip pkbylocuuf (knqpbzqjaw, 8 - 20)
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Core Patent

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Approval

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Regulation

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