This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
Search results
From Proteopedia
You searched for Thiadiazole
There is no page with the exact title "Thiadiazole". The search results for "Thiadiazole" are displayed below. You can create a page titled Thiadiazole (by clicking on the red link).
For more information about searching Proteopedia, see Help.
To exclude pages titled with 4-character PDB codes, use the checkbox "only Human created pages" at the bottom of this page.
Showing below up to 20 results starting with #1.
View (previous 20) (next 20) (20 | 50 | 100 | 250 | 500)
Article title matches
- Category:4-thiadiazole-2-sulfonamide (58 bytes)
1: List of pages with the keyword 4-thiadiazole-2-sulfonamide - Category:Thiadiazole (42 bytes)
1: List of pages with the keyword Thiadiazole - Category:Thiadiazole derivatives inhibitor (64 bytes)
1: List of pages with the keyword Thiadiazole derivatives inhibitor
Page text matches
- 2bz9 (5,243 bytes)
24: ...rties similar to those of EPBA, 2-(benzo[d]-2,1,3-thiadiazole-4-sulfonyl)-2-amino-2-phenyl-N-(pyridinyl-4) -ace... - 2usn (5,349 bytes)
2: ... OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THIADIAZOLE INHIBITOR PNU-141803==
26: ...the proteinase active site. Nitrogen atoms in the thiadiazole moiety make specific hydrogen bond interactions w...
28: Structural characterizations of nonpeptidic thiadiazole inhibitors of matrix metalloproteinases reveal th... - 1usn (5,348 bytes)
2: ... OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THIADIAZOLE INHIBITOR PNU-142372==
26: ...the proteinase active site. Nitrogen atoms in the thiadiazole moiety make specific hydrogen bond interactions w...
28: Structural characterizations of nonpeptidic thiadiazole inhibitors of matrix metalloproteinases reveal th... - 2ci0 (5,483 bytes)
24: ...rties similar to those of EPBA, 2-(benzo[d]-2,1,3-thiadiazole-4-sulfonyl)-2-amino-2-phenyl-N-(pyridinyl-4) -ace... - 2cib (5,527 bytes)
24: ...rties similar to those of EPBA, 2-(benzo[d]-2,1,3-thiadiazole-4-sulfonyl)-2-amino-2-phenyl-N-(pyridinyl-4) -ace... - 2eu2 (5,127 bytes)
26: ...e spacer groups allow novel binding modes for the thiadiazole moiety compared with conventional CAIs. - 2eu3 (5,117 bytes)
26: ...e spacer groups allow novel binding modes for the thiadiazole moiety compared with conventional CAIs. - 2hnc (5,430 bytes)
2: ...ic anhydrase II in complex with the 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor.==
7: ...gandDat"><scene name='pdbligand=1SA:5-AMINO-1,3,4-THIADIAZOLE-2-SULFONAMIDE'>1SA</scene>, <scene name='pdbligan...
26: ...onic anhydrase (CA, EC 4.2.1.1) are reported. The thiadiazole-sulfonamide moiety of the two compounds binds in ...
28: ...4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfona mide to human isoform II.,Menchise V, D... - 2hoc (5,512 bytes)
2: ...4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide inhibitor==
7: ...INO-3-CHLORO-5-FLUOROPHENYL)SULFONYL]AMINO}-1,3,4-THIADIAZOLE-2-SULFONAMIDE'>1CN</scene>, <scene name='pdbligan...
26: ...onic anhydrase (CA, EC 4.2.1.1) are reported. The thiadiazole-sulfonamide moiety of the two compounds binds in ...
28: ...4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfona mide to human isoform II.,Menchise V, D... - 3usn (5,640 bytes)
2: ...HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THE THIADIAZOLE INHIBITOR IPNU-107859, NMR, 1 STRUCTURE==
26: ... inhibitor. Binding interactions observed for the thiadiazole class of ligands have implications for the design...
28: Solution structures of stromelysin complexed to thiadiazole inhibitors.,Stockman BJ, Waldon DJ, Gates JA, Sca... - 1t26 (5,427 bytes)
2: ...drogenase complexed with NADH and 4-hydroxy-1,2,5-thiadiazole-3-carboxylic acid==
7: ...ndDat"><scene name='pdbligand=GBD:4-HYDROXY-1,2,5-THIADIAZOLE-3-CARBOXYLIC+ACID'>GBD</scene>, <scene name='pdbl... - 2pj9 (4,956 bytes)
2: ...B 2-(3-Aminomethyl-phenyl)-3-{[(R)-1-(benzo[1,2,5]thiadiazole-4-sulfonylamino)-2-methyl-propyl]-hydroxy-phosphi... - 3bl0 (4,089 bytes)
2: ...ibitors. Interaction of 2-N,N-Dimethylamino-1,3,4-thiadiazole-5-methanesulfonamide with twelve mammalian isofor... - 2w0u (4,527 bytes)
2: ...THE INHIBITOR 5-[(4-CHLOROPHENYL)SULFANYL]- 1,2,3-THIADIAZOLE-4-CARBOXYLATE.==
7: ...'pdbligand=C7C:5-[(4-CHLOROPHENYL)SULFANYL]-1,2,3-THIADIAZOLE-4-CARBOXYLATE'>C7C</scene>, <scene name='pdbligan...
24: ...with 4-carboxy-5-[(4-chlorophenyl)sulfanyl]-1,2,3-thiadiazole (CCPST) has been determined at 2.8 A resolution. ...
26: ...itor 4-carboxy-5-[(4-chlorophenyl)sulfanyl]-1,2,3-thiadiazole.,Bourhis JM, Vignaud C, Pietrancosta N, Gueritte ... - 3hlj (5,692 bytes)
26: ... strength of a series of benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulphonamides were determined for recombinant h...
28: ...ozymes I, II and IX with benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulphonamides.,Baranauskiene L, Hilvo M, Matuli... - User:Gisselle Medina/Sandbox1 Carbonic Anhydrase (3,601 bytes)
8: ...th the nitrogen-hydrogen backbone of Thr 199. The thiadiazole ring forms strong van der Waals interactions with... - Category:4-thiadiazole-2-sulfonamide (58 bytes)
1: List of pages with the keyword 4-thiadiazole-2-sulfonamide - Category:Thiadiazole (42 bytes)
1: List of pages with the keyword Thiadiazole - 3mhc (5,539 bytes)
26: ...f 5-carboxamide- and sufonamide-derivatized 1,3,4-thiadiazole-2-sulfonamides and offers a hot spot for designin... - Heat Shock Protein structures (27,185 bytes)
247: ...i5]], [[2yi6]], [[2yi7]], [[5fnd]] - hHsp90 NTD + thiadiazole derivative<br />
View (previous 20) (next 20) (20 | 50 | 100 | 250 | 500)
You may also try
