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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H12Cl2F3N7O2S
Molecular Weight 506.289
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Tovorafenib

SMILES

C[C@@H](NC(=O)C1=NC=NC(N)=C1Cl)C2=NC=C(S2)C(=O)NC3=CC(=C(Cl)C=N3)C(F)(F)F

InChI

InChIKey=VWMJHAFYPMOMGF-ZCFIWIBFSA-N
InChI=1S/C17H12Cl2F3N7O2S/c1-6(28-15(31)12-11(19)13(23)27-5-26-12)16-25-4-9(32-16)14(30)29-10-2-7(17(20,21)22)8(18)3-24-10/h2-6H,1H3,(H,28,31)(H2,23,26,27)(H,24,29,30)/t6-/m1/s1

HIDE SMILES / InChI

Molecular Formula C17H12Cl2F3N7O2S
Molecular Weight 506.289
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: Description was created based on several sources, including https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=710688

BIIB-024, also known as MLN2480, and AMG 2112819, is an oral, selective pan-Raf kinase inhibitor. The Raf kinases (A-Raf, B-Raf and C-Raf) are key regulators of cell proliferation and survival within the mitogen-activated protein kinase (MAPK) pathway. The MAPK pathway is frequently disregulated in human cancers, often via activating mutations of Ras or Raf. BIIB-024 inhibits MAPK pathway signaling in BRAF mutant and some RAS mutant preclinical cancer models at concentrations that are tolerated in vivo. BIIB-024 is most potent in BRAF mutant melanoma models but also has single agent activity in some RAS mutant models. The combination of BIIB-024 with TAK-733 inhibits the growth of a broader range of RAS mutant tumor models than single agent BIIB-024, including primary human tumor xenograft models of melanoma and CRC. BIIB-024 is in phase I clinical trials for the treatment of malignant melanoma and solid tumours.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
Patents

Sample Use Guides

100 mg, tablets, orally, once on protocol specified days of a 28-day Cycle for up to 12 Cycles
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: BIIB024 was screened against the Millipore KinaseProfiler full panel screen (222 unique human kinases) at 10 μM. Kinases most potently inhibited were then tested at 1.0 and 0.2 uM and IC50 values were determined on kinases most potently inhibited.
BIIB-024 inhibits a small subset of kinases in a similar range as Raf kinases (IC50 1-50 nM)
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:25:09 UTC 2023
Edited
by admin
on Sat Dec 16 01:25:09 UTC 2023
Record UNII
ZN90E4027M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Tovorafenib
USAN  
Official Name English
BIIB024
Code English
DAY-101
Code English
tovorafenib [INN]
Common Name English
TOVORAFENIB [USAN]
Common Name English
4-Pyrimidinecarboxamide, 6-amino-5-chloro-N-[(1R)-1-[5-[[[5-chloro-4-(trifluoromethyl)-2-pyridinyl]amino]carbonyl]-2-thiazolyl]ethyl]-
Systematic Name English
DAY101
Code English
6-amino-5-chloro-N-{(1R)-1-(5-{[5-chloro-4-(trifluoromethyl)pyridin-2-yl]carbamoyl}thiazol-2-yl)ethyl}pyrimidine-4-carboxamide
Systematic Name English
TAK-580
Code English
BIIB-024
Code English
MLN-2480
Code English
Classification Tree Code System Code
FDA ORPHAN DRUG 410813
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
FDA ORPHAN DRUG 768320
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL3348923
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
PUBCHEM
25161177
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
EPA CompTox
DTXSID70149011
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
USAN
JK-261
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
CAS
1096708-71-2
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
FDA UNII
ZN90E4027M
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
CHEBI
167672
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
INN
11985
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
NCI_THESAURUS
C106254
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
SMS_ID
100000183294
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
DRUG BANK
DB15266
Created by admin on Sat Dec 16 01:25:09 UTC 2023 , Edited by admin on Sat Dec 16 01:25:09 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
TARGET->WEAK INHIBITOR
IC50
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY