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Details

Stereochemistry EPIMERIC
Molecular Formula C44H49F2N11O6
Molecular Weight 865.9268
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of KT-474

SMILES

CN1C(=O)N(C2CCC(=O)NC2=O)C3=C1C(=CC=C3)C#CCOC4CCN(C[C@H]5CC[C@@H](CC5)N6C=C(NC(=O)C7=C8N=C(C=CN8N=C7)N9C[C@H]%10C[C@@H]9CO%10)C(=N6)C(F)F)CC4

InChI

InChIKey=NQGKNAVUMAHSQN-KDRPOVOJSA-N
InChI=1S/C44H49F2N11O6/c1-52-39-27(4-2-6-34(39)57(44(52)61)35-11-12-37(58)50-43(35)60)5-3-19-62-30-13-16-53(17-14-30)22-26-7-9-28(10-8-26)56-24-33(38(51-56)40(45)46)48-42(59)32-21-47-55-18-15-36(49-41(32)55)54-23-31-20-29(54)25-63-31/h2,4,6,15,18,21,24,26,28-31,35,40H,7-14,16-17,19-20,22-23,25H2,1H3,(H,48,59)(H,50,58,60)/t26-,28-,29-,31-,35?/m1/s1

HIDE SMILES / InChI

Molecular Formula C44H49F2N11O6
Molecular Weight 865.9268
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 4 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 09:27:26 GMT 2025
Edited
by admin
on Wed Apr 02 09:27:26 GMT 2025
Record UNII
2SXR65P7E3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SAR-444656
Preferred Name English
KT-474
Code English
SAR444656
Code English
PYRAZOLO(1,5-A)PYRIMIDINE-3-CARBOXAMIDE, N-(3-(DIFLUOROMETHYL)-1-(TRANS-4-((4-((3-(1-(2,6-DIOXO-3-PIPERIDINYL)-2,3-DIHYDRO-3-METHYL-2-OXO-1H-BENZIMIDAZOL-4-YL)-2-PROPYN-1-YL)OXY)-1-PIPERIDINYL)METHYL)CYCLOHEXYL)-1H-PYRAZOL-4-YL)-5-(1R,4R)-2-OXA-5-AZABICY
Systematic Name English
Code System Code Type Description
CAS
2432994-31-3
Created by admin on Wed Apr 02 09:27:26 GMT 2025 , Edited by admin on Wed Apr 02 09:27:26 GMT 2025
PRIMARY
SMS_ID
300000050941
Created by admin on Wed Apr 02 09:27:26 GMT 2025 , Edited by admin on Wed Apr 02 09:27:26 GMT 2025
PRIMARY
FDA UNII
2SXR65P7E3
Created by admin on Wed Apr 02 09:27:26 GMT 2025 , Edited by admin on Wed Apr 02 09:27:26 GMT 2025
PRIMARY
Related Record Type Details
TARGET->DEGRADER
KT-474 is a targeting IRAK4 and the E3 ligase CRBN to mediate the selective degradation of IRAK4 via the ubiquitin-proteasome system (UPS)
TARGET->LIGAND
Related Record Type Details
ACTIVE MOIETY