2-[2-[carboxymethyl-[2-keto-2-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)amino]ethyl]amino]ethyl-[2-keto-2-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)amino]ethyl]amino]acetic acid
Compound with spectra: 1 NMR
![2-[2-[carboxymethyl-[2-keto-2-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)amino]ethyl]amino]ethyl-[2-keto-2-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)amino]ethyl]amino]acetic acid](/api/compound/HAYD4BKI3EA.png?ph=true&h=300&w=458 "2-[2-[carboxymethyl-[2-keto-2-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)amino]ethyl]amino]ethyl-[2-keto-2-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)amino]ethyl]amino]acetic acid")
| SpectraBase Compound ID | HAYD4BKI3EA |
|---|---|
| InChI | InChI=1S/C14H20N10O10S4/c15-37(31,32)13-21-19-11(35-13)17-7(25)3-23(5-9(27)28)1-2-24(6-10(29)30)4-8(26)18-12-20-22-14(36-12)38(16,33)34/h1-6H2,(H,27,28)(H,29,30)(H2,15,31,32)(H2,16,33,34)(H,17,19,25)(H,18,20,26) |
| InChIKey | KTKGBEYRKDMODK-UHFFFAOYSA-N |
| Mol Weight | 616.6 g/mol |
| Molecular Formula | C14H20N10O10S4 |
| Exact Mass | 616.024672 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O:KOD |
2-[2-(bis(carboxymethyl)amino)ethyl-[2-keto-2-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)amino]ethyl]amino]acetic acid
2-(4-Amino-5-thioxo-4,5-dihydro-[1,2,4]triazol-1-yl)-N-(5-methyl-[1,3,4]thiadiazol-2-yl)-acetamide
N-(5-ethyl-1,3,4-thiadiazol-2-yl)-4-{4-[2-(4-methylphenoxy)ethyl]-1-piperazinyl}-4-oxobutanamide
N~1~-(2-furylmethyl)-N~2~-(5-propyl-1,3,4-thiadiazol-2-yl)ethanediamide
acetamide, 2-[(3-amino-1H-1,2,4-triazol-5-yl)thio]-N-[5-[(phenylmethyl)thio]-1,3,4-thiadiazol-2-yl]-
4-(4-benzyl-1-piperazinyl)-N-(5-ethyl-1,3,4-thiadiazol-2-yl)-4-oxobutanamide
acetamide, 2-[(4,5-dimethyl-1H-imidazol-2-yl)thio]-N-[5-[(phenylmethyl)thio]-1,3,4-thiadiazol-2-yl]-
2-(2,4-dichlorophenoxy)-N-[5-(ethylsulfanyl)-1,3,4-thiadiazol-2-yl]acetamide
Butyric acid, 2-acetylamino-4-methylsulfanyl-, (5-isopropyl-[1,3,4]thiadiazol-2-ylcarbamoyl)methyl ester
4-(4-cyclopentyl-1-piperazinyl)-N-(5-isopropyl-1,3,4-thiadiazol-2-yl)-4-oxobutanamide
| Title | Journal or Book | Year |
|---|---|---|
| Carbonic Anhydrase Inhibitors. A General Approach for the Preparation of Water-Soluble Sulfonamides Incorporating Polyamino−Polycarboxylate Tails and of Their Metal Complexes Possessing Long-Lasting, Topical Intraocular Pressure-Lowering Properties | Journal of Medicinal Chemistry | 2002 |