Browse Synthetic Compounds

NO. IPAD-DB ID Name Target-protein Molecular Formula 2D Structure Ref. Link
376 S00376 (Z)-1-Cyclopropyl-3-(2-(4-isopropylphenyl)hydrazono)-5-methoxyindolin-2-one
377 S00377 S-4
378 S00378 16-oxo-paraherquamide
379 S00379 5-chloro-3-[4-(3-diethylaminopropoxy)benzoyl]-2-(4-methoxyphnyl)benzofuran
380 S00380 2-[4'-(3-diethylaminopropoxy)-phenyl]-benzofuran
381 S00381 Graphene oxide
382 S00382 (22R, 25R)-3b-(N-benzylcarboxylate)-5-en-20a-spirostan
383 S00383 Imidazolium [trans-RuCl4(1H-imidazole)2]
384 S00384 2-Methylimidazolium [trans-RuCl4(2-methyl-1H-imidazole)2]
385 S00385 Imidazolium [trans-RuCl4(DMSO-S)(1H-imidazole)]
386 S00386 2-Methylimidazolium [trans-RuCl4(DMSO-S)(2-methyl-1H-imidazole)]
387 S00387 CSB6B
388 S00388 Avenanthramide-C(Avn-C)
389 S00389 N, N’-(1, 2-phenylene)bis(1-(1H-imidazol-4-yl)methanimine)
390 S00390 2-(3, 4-Dihydroxyphenethyl)-1H-benzo[de]isoquinoline-1, 3(2H)dione
391 S00391 Promazine hydrochloride -
392 S00392 Lacmoid -
393 S00393 2-[4-(Dimethylamino)phenyl]-6-methylbenzothiazole -
394 S00394 3, 3′-Dipropyl thiodicarbocyanine iodide -
395 S00395 Ferric dehydroporphyrin IX -
396 S00396 1-(2-Fluorobenzyl)-4-((4-oxo-4-((4-phenylthiazol-2-yl)amino)butanamido)methyl) pyridin-1-ium chloride
397 S00397 1-(2-Bromobenzyl)-4-((4-oxo-4-((4-phenylthiazol-2-yl)amino)butanamido)methyl) pyridin-1-ium bromide
398 S00398 JFD03947  -
399 S00399 3-Ethyl-2-[(3-{3-ethyl-5-[3-(nitrooxy)propyloxy]-1, 3-benzothiazol-2(3H)-ylidene}prop-1-en-1-yl]-1, 3-benzothiazol-3-ium iodide
400 S00400 3-Ethyl-2-[(3-{3-ethyl-5-[(3-phenylfuroxan-4-yl)oxy]-1, 3-benzothiazol-2(3H)-ylidene}prop-1-en-1-yl]-1, 3-benzothiazol-3-ium iodide