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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H18ClF2N5O3
Molecular Weight 449.838
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ASCIMINIB

SMILES

O[C@@H]1CCN(C1)C2=C(C=C(C=N2)C(=O)NC3=CC=C(OC(F)(F)Cl)C=C3)C4=CC=NN4

InChI

InChIKey=VOVZXURTCKPRDQ-CQSZACIVSA-N
InChI=1S/C20H18ClF2N5O3/c21-20(22,23)31-15-3-1-13(2-4-15)26-19(30)12-9-16(17-5-7-25-27-17)18(24-10-12)28-8-6-14(29)11-28/h1-5,7,9-10,14,29H,6,8,11H2,(H,25,27)(H,26,30)/t14-/m1/s1

HIDE SMILES / InChI
ABL-001 (asciminib), a potent and selective allosteric tyrosine-protein kinase ABL1 inhibitor that is undergoing clinical development testing in patients with Chronic myeloid leukemia (CML) and Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia. is a tyrosine-protein kinase ABL1 inhibitor. In contrast to catalytic-site ABL1 kinase inhibitors, ABL001 binds to the myristoyl pocket of ABL1 and induces the formation of an inactive kinase conformation. ABL001 and second-generation catalytic inhibitors have similar cellular potencies but distinct patterns of resistance mutations, with genetic barcoding studies revealing pre-existing clonal populations with no shared resistance between ABL001 and the catalytic inhibitor nilotinib. ABL001 was tested on mice with a particularly aggressive type of CML. The combination of ABL001 and nilotinib led to complete disease control and eradicated CML xenograft tumors without recurrence after the cessation of treatment. ABL001 is being tested in clinical trials for treatment of CML and Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia alone and in combination with niotinib, imatinib or dasatinib.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P00519
Gene ID: 25.0
Gene Symbol: ABL1
Target Organism: Homo sapiens (Human)
1.3 nM [IC50]
Conditions

Conditions

PubMed

PubMed

TitleDatePubMed
Second line small molecule therapy options for treating chronic myeloid leukemia.
2017 Jan
Identification and characterization of activating ABL1 1b kinase mutations: impact on sensitivity to ATP-competitive and allosteric ABL1 inhibitors.
2017 May
Patents

Sample Use Guides

40 mg ABL001 twice a day administered in adult patients with Chronic Myelogenous Leukemia
Route of Administration: Oral
BL001 potently inhibited the proliferation of Ba/F3 cells expressing native BCR-ABL1 or a variety of BCR-ABL1 point mutations (IC50 range: 1.3-113.5 nM), with no observed toxicity to parental Ba/F3 cells up to 10 uM. Interestingly, however, ABL001 demonstrated little to no activity against a small panel of BCR-ABL1 compound mutations tested (G250E/T315I, E255K/T315I, E255V/T315I).
Name Type Language
ASCIMINIB
INN   WHO-DD  
USAN   INN  
Official Name English
Asciminib [WHO-DD]
Common Name English
ABL-001
Code English
ABL001
Code English
N-(4-(CHLORODIFLUOROMETHOXY)PHENYL)-6-((3R)-3- HYDROXYPYRROLIDIN-1-YL)-5-(1H-PYRAZOL-3-YL)PYRIDINE- 3-CARBOXAMIDE
Systematic Name English
asciminib [INN]
Common Name English
3-PYRIDINECARBOXAMIDE, N-(4-(CHLORODIFLUOROMETHOXY)PHENYL)-6-((3R)-3-HYDROXY-1-PYRROLIDINYL)-5-(1H-PYRAZOL-3-YL)-
Systematic Name English
NVP-ABL001
Code English
ABL001-NX
Code English
ASCIMINIB [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1967
Created by admin on Sat Dec 16 18:03:02 GMT 2023 , Edited by admin on Sat Dec 16 18:03:02 GMT 2023
FDA ORPHAN DRUG 556416
Created by admin on Sat Dec 16 18:03:02 GMT 2023 , Edited by admin on Sat Dec 16 18:03:02 GMT 2023
NCI_THESAURUS C129825
Created by admin on Sat Dec 16 18:03:02 GMT 2023 , Edited by admin on Sat Dec 16 18:03:02 GMT 2023
Code System Code Type Description
FDA UNII
L1F3R18W77
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ChEMBL
CHEMBL3545115
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SMS_ID
100000174619
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RXCUI
2584304
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USAN
FG-57
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NCI_THESAURUS
C114494
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PRIMARY
CAS
1492952-76-7
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DRUG BANK
DB12597
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PUBCHEM
72165228
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INN
10267
Created by admin on Sat Dec 16 18:03:02 GMT 2023 , Edited by admin on Sat Dec 16 18:03:02 GMT 2023
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DAILYMED
L1F3R18W77
Created by admin on Sat Dec 16 18:03:02 GMT 2023 , Edited by admin on Sat Dec 16 18:03:02 GMT 2023
PRIMARY