Ligand · J1T
J1T · 4-[4-[(1~{R})-1-(6-methoxy-1,3-benzodioxol-5-yl)-2-pyrrolidin-1-yl-ethyl]phenyl]-~{N}-[4-[[(2~{R})-4-morpholin-4-yl-1-phenylsulfanyl-butan-2-yl]amino]-3-(trifluoromethylsulfonyl)phenyl]sulfonyl-benzamide
J1T, 4-[4-[(1~{R})-1-(6-methoxy-1,3-benzodioxol-5-yl)-2-pyrrolidin-1-yl-ethyl]phenyl]-~{N}-[4-[[(2~{R})-4-morpholin-4-yl-1-phenylsulfanyl-butan-2-yl]amino]-3-(trifluoromethylsulfonyl)phenyl]sulfonyl-benzamide (C48 H51 F3 N4 O9 S3, 981.1…
- Component
- J1T
- Formula
- C48 H51 F3 N4 O9 S3
- Class
- ligand
- Structures
- 1
- PDB entries
- 1
Binding sites
J1T in 1 structure; the first of them:
- 6QGJ · Structure of human BCL-2 in complex with FRAGMENT/ABT-263 hybrid · J1T A301 · binds ALA100, PHE104, TYR108, ASP111, LEU137, ASN143, TRP144, GLY145 and 10 more
Residues it binds most
ASN 1, PHE 1, GLY 1, LEU 1, TYR 1, ALA 1, ARG 1, ASP 1, GLU 1, TRP 1 (residue and the binding sites it lines).
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