Drug (ID: DG01479) and It's Reported Resistant Information
Name
NSC348884
Synonyms
NSC348884; 81624-55-7; NSC 348884; NSC-348884; N,N,N',N'-tetrakis[(6-methyl-1H-benzimidazol-2-yl)methyl]ethane-1,2-diamine; NSC348884 hydrate; CHEMBL4584341; SCHEMBL12126212; DTXSID90319638; BCP09001; EX-A2342; s8149; ZINC77029766; BCP9000996; CCG-270304; CS-5564; LP01178; SDCCGSBI-0633803.P001; NSC 348884; AC-32976; BS-17560; HY-13915; C76613; N,N',N'-tetrakis[(6-methyl-1H-benzimidazol-2-yl)methyl]ethane-1,2-diamine; N,N,N',N'-Tetrakis-(5-methyl-1H-benzoimidazol-2-ylmethyl)-ethane-1,2-diamine; N1,N1,N2,N2-Tetrakis((6-methyl-1H-benzo[d]imidazol-2-yl)methyl)ethane-1,2-diamine; (2-{bis[(6-methyl-1H-1,3-benzodiazol-2-yl)methyl]amino}ethyl)bis[(6-methyl-1H-1,3-benzodiazol-2-yl)methyl]amine
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Structure
Target . NOUNIPROTAC [1]
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Formula
11
IsoSMILES
CC1=CC2=C(C=C1)N=C(N2)CN(CCN(CC3=NC4=C(N3)C=C(C=C4)C)CC5=NC6=C(N5)C=C(C=C6)C)CC7=NC8=C(N7)C=C(C=C8)C
InChI
InChI=1S/C38H40N10/c1-23-5-9-27-31(15-23)43-35(39-27)19-47(20-36-40-28-10-6-24(2)16-32(28)44-36)13-14-48(21-37-41-29-11-7-25(3)17-33(29)45-37)22-38-42-30-12-8-26(4)18-34(30)46-38/h5-12,15-18H,13-14,19-22H2,1-4H3,(H,39,43)(H,40,44)(H,41,45)(H,42,46)
InChIKey
KZOLQEUQAFTQFM-UHFFFAOYSA-N
PubChem CID
335974
Type(s) of Resistant Mechanism of This Drug
  ADTT: Aberration of the Drug's Therapeutic Target
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-02: Benign/in-situ/malignant neoplasm
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Acute myeloid leukemia [ICD-11: 2A60]
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Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
       Aberration of the Drug's Therapeutic Target (ADTT) Click to Show/Hide
Key Molecule: Nucleophosmin (NPM1) [1]
Molecule Alteration FS-deletion
p.W288fs (c.863_864)
Sensitive Disease Acute myeloid leukemia [ICD-11: 2A60.0]
Experimental Note Revealed Based on the Cell Line Data
In Vitro Model OCI-AML3 cells Blood Homo sapiens (Human) CVCL_1844
HL-60 cells Peripheral blood Homo sapiens (Human) CVCL_0002
Experiment for
Molecule Alteration
Immunoblotting analysis
Experiment for
Drug Resistance
Colony-forming assay
Mechanism Description The fs-deletion p.W288fs (c.863_864) in gene NPM1 cause the sensitivity of NSC348884 by aberration of the drug's therapeutic target.
References
Ref 1 Targeting levels or oligomerization of nucleophosmin 1 induces differentiation and loss of survival of human AML cells with mutant NPM1Blood. 2011 Sep 15;118(11):3096-106. doi: 10.1182/blood-2010-09-309674. Epub 2011 Jun 30.

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