In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
July 24th, 2004 | 24 | No |
1-(4-Chloro-3-sulfamoylbenzamido)-2-methylindoline
26807-65-8; CPD000058829; INDAPAMIDE; SAM002564214
26807-65-8; D00345; Indapamide (JP16/USP); Lozol (TN); Natrix (TN)
3-(Aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)benzamide
4-Chloro-N-(2-methyl-1-indolinyl)-3-sulfamoylbenzamide
4-chloro-N-(2-methyl-2,3-dihydroindol-1-yl)-3-sulfamoylbenzamide
4-chloro-N-[(2S)-2-methyl-2,3-dihydro-1H-indol-1-yl]-3-sulfamoylbenzamide
5-20-06-00348 (Beilstein Handbook Reference)
Arifon, Fludex, Noranat, Veroxil, Tertensif
benzamide, 3-(aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)-
Benzamide, 3-(aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)- (9CI)
Benzamide, 3-(aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-l-yl)-
BENZAMIDE, 4-CHLORO-N-(2-METHYL-1-INDOLINYL)-3-SULFAMOYL-
CPD000058829; Indapamide; SAM002564214
D06401; Indapamide hydrate; Tenaxil (TN)
Indapamida [INN-Spanish]; Indapamidum [INN-Latin]
Indapamida [INN-Spanish];Indapamidum [INN-Latin]
N-(4-Chloro-3-sulfamoylbenzamido)-2-methylindoline
N-[4-Chloro-3-sulfamoylbenzamido]-2- methylindoline
NLozol, Arifon, Fludex, Noranat, Veroxil, Tertensif, Indapamide
Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
---|---|---|---|---|---|---|---|---|---|---|
Ref Reference (pH 7) | 2.46 | 3.92 | -19.14 | 3 | 6 | 0 | 93 | 365.842 | 3 | ↓ |
Note Type | Comments | Provided By |
---|---|---|
MP | 170 | TCI |
ALOGPS_SOLUBILITY | 3.42e-02 g/l | DrugBank-approved |
Purity | 97% | Fluorochem |
Therapy | diuretic, antihypertensive | SMDC Iconix |
PUBCHEM_PATENT_ID | EP0083371A1; EP0424445B1; EP0509184A1; EP0745265A1; EP0745265B1; EP0803275A1; EP0803469A1; EP0852978A1; EP0987552A2; EP0987552A3; US4049920; US4437190; US5105372; US5472146; US5544091; US5565931; US5668134; US5912257; US6071838; WO1983000093A1; WO19850038 | IBM Patent Data |
Indications | hpyertension | KeyOrganics Bioactives |
PUBCHEM_SUBSTANCE_COMMENT | NCC_SAMPLE_SUPPLIER : LightBiologicals; NCC_SUPPLIER_STRUCTURE_ID : I-0114; NCC_SUPPLIER_SAMPLE_COMMENTS : OFF-WHITE POWDER | NIH Clinical Collection via PubChem |
Target | Others | Selleck Chemicals |
PUBCHEM_SUBSTANCE_COMMENT | SAMPLE_SUPPLIER: LightBiologicals; SUPPLIER_STRUCTURE_ID: I-0114; SUPPLIER_COMMENTS: OFF-WHITE POWDER | NIH Clinical Collection via PubChem |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CAH1-1-E | Carbonic Anhydrase I (cluster #1 Of 12), Eukaryotic | Eukaryotes | 10000 | 0.29 | Binding ≤ 10μM |
CAH12-1-E | Carbonic Anhydrase XII (cluster #1 Of 9), Eukaryotic | Eukaryotes | 10 | 0.47 | Binding ≤ 10μM |
CAH13-1-E | Carbonic Anhydrase XIII (cluster #1 Of 7), Eukaryotic | Eukaryotes | 13 | 0.46 | Binding ≤ 10μM |
CAH14-1-E | Carbonic Anhydrase XIV (cluster #1 Of 8), Eukaryotic | Eukaryotes | 4950 | 0.31 | Binding ≤ 10μM |
CAH2-1-E | Carbonic Anhydrase II (cluster #1 Of 15), Eukaryotic | Eukaryotes | 300 | 0.38 | Binding ≤ 10μM |
CAH4-1-E | Carbonic Anhydrase IV (cluster #1 Of 16), Eukaryotic | Eukaryotes | 213 | 0.39 | Binding ≤ 10μM |
CAH5A-1-E | Carbonic Anhydrase VA (cluster #1 Of 10), Eukaryotic | Eukaryotes | 890 | 0.35 | Binding ≤ 10μM |
CAH5B-1-E | Carbonic Anhydrase VB (cluster #1 Of 9), Eukaryotic | Eukaryotes | 274 | 0.38 | Binding ≤ 10μM |
CAH6-1-E | Carbonic Anhydrase VI (cluster #1 Of 8), Eukaryotic | Eukaryotes | 1606 | 0.34 | Binding ≤ 10μM |
CAH7-1-E | Carbonic Anhydrase VII (cluster #1 Of 8), Eukaryotic | Eukaryotes | 300 | 0.38 | Binding ≤ 10μM |
CAH9-1-E | Carbonic Anhydrase IX (cluster #1 Of 11), Eukaryotic | Eukaryotes | 36 | 0.43 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CAH2_HUMAN | P00918 | Carbonic Anhydrase II, Human | 200 | 0.39 | Binding ≤ 1μM |
CAH4_HUMAN | P22748 | Carbonic Anhydrase IV, Human | 213 | 0.39 | Binding ≤ 1μM |
CAH9_HUMAN | Q16790 | Carbonic Anhydrase IX, Human | 36 | 0.43 | Binding ≤ 1μM |
CAH5A_HUMAN | P35218 | Carbonic Anhydrase VA, Human | 890 | 0.35 | Binding ≤ 1μM |
CAH5B_HUMAN | Q9Y2D0 | Carbonic Anhydrase VB, Human | 274 | 0.38 | Binding ≤ 1μM |
CAH7_HUMAN | P43166 | Carbonic Anhydrase VII, Human | 0.23 | 0.56 | Binding ≤ 1μM |
CAH12_HUMAN | O43570 | Carbonic Anhydrase XII, Human | 10 | 0.47 | Binding ≤ 1μM |
CAH13_HUMAN | Q8N1Q1 | Carbonic Anhydrase XIII, Human | 100 | 0.41 | Binding ≤ 1μM |
CAH13_MOUSE | Q9D6N1 | Carbonic Anhydrase XIII, Mouse | 13 | 0.46 | Binding ≤ 1μM |
CAH1_HUMAN | P00915 | Carbonic Anhydrase I, Human | 10000 | 0.29 | Binding ≤ 10μM |
CAH2_HUMAN | P00918 | Carbonic Anhydrase II, Human | 200 | 0.39 | Binding ≤ 10μM |
CAH4_HUMAN | P22748 | Carbonic Anhydrase IV, Human | 213 | 0.39 | Binding ≤ 10μM |
CAH9_HUMAN | Q16790 | Carbonic Anhydrase IX, Human | 36 | 0.43 | Binding ≤ 10μM |
CAH5A_HUMAN | P35218 | Carbonic Anhydrase VA, Human | 890 | 0.35 | Binding ≤ 10μM |
CAH5B_HUMAN | Q9Y2D0 | Carbonic Anhydrase VB, Human | 274 | 0.38 | Binding ≤ 10μM |
CAH6_HUMAN | P23280 | Carbonic Anhydrase VI, Human | 1606 | 0.34 | Binding ≤ 10μM |
CAH7_HUMAN | P43166 | Carbonic Anhydrase VII, Human | 0.23 | 0.56 | Binding ≤ 10μM |
CAH12_HUMAN | O43570 | Carbonic Anhydrase XII, Human | 10 | 0.47 | Binding ≤ 10μM |
CAH13_HUMAN | Q8N1Q1 | Carbonic Anhydrase XIII, Human | 100 | 0.41 | Binding ≤ 10μM |
CAH13_MOUSE | Q9D6N1 | Carbonic Anhydrase XIII, Mouse | 13 | 0.46 | Binding ≤ 10μM |
CAH14_HUMAN | Q9ULX7 | Carbonic Anhydrase XIV, Human | 4950 | 0.31 | Binding ≤ 10μM |
Description | Species |
---|---|
Erythrocytes take up carbon dioxide and release oxygen | |
Erythrocytes take up oxygen and release carbon dioxide | |
Regulation of gene expression by Hypoxia-inducible Factor | |
Reversible hydration of carbon dioxide |