U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C24H30N6O6S2
Molecular Weight 562.662
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FHD-286

SMILES

COC[C@H](NC(=O)C1=CN(C=C1)S(C)(=O)=O)C(=O)NC2=NC(=CS2)C3=NC(=CC=C3)N4C[C@H](C)O[C@H](C)C4

InChI

InChIKey=JBLQNFBXKOAIHG-FCEWJHQRSA-N
InChI=1S/C24H30N6O6S2/c1-15-10-29(11-16(2)36-15)21-7-5-6-18(25-21)20-14-37-24(27-20)28-23(32)19(13-35-3)26-22(31)17-8-9-30(12-17)38(4,33)34/h5-9,12,14-16,19H,10-11,13H2,1-4H3,(H,26,31)(H,27,28,32)/t15-,16+,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H30N6O6S2
Molecular Weight 562.662
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:30:31 GMT 2023
Edited
by admin
on Sat Dec 16 17:30:31 GMT 2023
Record UNII
QHA5XLA4SA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FHD-286
Code English
1H-PYRROLE-3-CARBOXAMIDE, N-((1S)-2-((4-(6-((2R,6S)-2,6-DIMETHYL-4-MORPHOLINYL)-2-PYRIDINYL)-2-THIAZOLYL)AMINO)-1-(METHOXYMETHYL)-2-OXOETHYL)-1-(METHYLSULFONYL)-
Systematic Name English
Code System Code Type Description
NCI_THESAURUS
C179408
Created by admin on Sat Dec 16 17:30:31 GMT 2023 , Edited by admin on Sat Dec 16 17:30:31 GMT 2023
PRIMARY
SMS_ID
300000039148
Created by admin on Sat Dec 16 17:30:31 GMT 2023 , Edited by admin on Sat Dec 16 17:30:31 GMT 2023
PRIMARY
FDA UNII
QHA5XLA4SA
Created by admin on Sat Dec 16 17:30:31 GMT 2023 , Edited by admin on Sat Dec 16 17:30:31 GMT 2023
PRIMARY
PUBCHEM
156818030
Created by admin on Sat Dec 16 17:30:31 GMT 2023 , Edited by admin on Sat Dec 16 17:30:31 GMT 2023
PRIMARY
CAS
2671128-05-3
Created by admin on Sat Dec 16 17:30:31 GMT 2023 , Edited by admin on Sat Dec 16 17:30:31 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Potently and selectively inhibits the ATPase components of the BAF complex, resulting in BAF Inhibition.
ALLOSTERIC INHIBITOR
Related Record Type Details
ACTIVE MOIETY