Ligand · YFH
YFH · N-({4-[2-(4-{[(4R)-4'-chloro-4-methyl-6-{[4-(4-{[4-{[(2R)-4-[(1R,4R)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(phenylsulfanyl)butan-2-yl]amino}-3-(trifluoromethanesulfonyl)benzene-1-sulfonyl]carbamoyl}phenyl)piperazin-1-yl]methyl}-2,3,4,5-tetrahydro[1,1'-biphenyl]-4-yl]methyl}piperazin-1-yl)-2-oxoethyl]piperazin-1-yl}acetyl)-3-methyl-L-valyl-(4S)-4-hydroxy-N-{(1S)-1-[4-(4-methyl-1,3-thiazol-5-yl)phenyl]ethyl}-L-prolinamide
YFH, N-({4-[2-(4-{[(4R)-4'-chloro-4-methyl-6-{[4-(4-{[4-{[(2R)-4-[(1R,4R)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(phenylsulfanyl)butan-2-yl]amino}-3-(trifluoromethanesulfonyl)benzene-1-sulfonyl]carbamoyl}phenyl)piperazin-1-yl]methyl}-2,3,4…
- Component
- YFH
- Formula
- C83 H105 Cl F3 N13 O11 S4
- Class
- ligand
- Structures
- 1
- PDB entries
- 1
Binding sites
YFH in 1 structure; the first of them:
- 8FY2 · E3:PROTAC:target ternary complex structure (VCB/WH244/BCL-2) · YFH D301 · binds ASN67, ARG69, PHE76, PRO86, TRP88, PHE91, TYR98, PRO99 and 34 more
Residues it binds most
PHE 1, ARG 1, TYR 1, GLU 1, LEU 1, TRP 1, VAL 1, ALA 1, ASN 1, ASP 1 (residue and the binding sites it lines).
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