Drug Details
General Information of the Drug (ID: DR2202) | ||||
---|---|---|---|---|
Name |
Candesartan cilexetil
|
|||
Synonyms |
Candesartan cilexetil; 145040-37-5; Atacand; TCV-116; Amias; Parapres; Kenzen; candesartancilexetil; CANDESARTAN CILEXTIL; TCV 116; C33H34N6O6; CHEMBL1014; CHEBI:3348; 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2'-(2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate; TCY 116; MFCD00871371; 1-(cyclohexyloxycarbonyloxy)ethyl 1-((2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate; 1-cyclohexyloxycarbonyloxyethyl 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate; 1-(((cyclohexyloxy)carbonyl)oxy)ethyl 1-((2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate; 2-Ethoxy-3-[2'-(1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid 1-cyclohexyloxycarbonyloxy-ethyl ester; 1-[[(cyclohexyloxy)carbonyl]oxy]ethyl 2-ethoxy-1-[[2'-(1h-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1h-benzimidazole-7-carboxylate; 2-ETHOXY-1-[[2'-(2H-TETRAZOL-5-YL)[1,1'-BIPHENYL]-4-YL]METHYL]-1H-BENZIMIDAZOLE-7-CARBOXYLIC ACID 1-[[(CYCLOHEXYLOXY)CARBONYL]OXY]ETHYL ESTER; Candesartan cilexetil [USAN]; Racanda; Candesartan hexetil; 1-cyclohexyloxycarbonyloxyethyl 2-ethoxy-3-[[4-[2-(1H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate; Atacand (TN); candesartan cilexitil; Spectrum_001707; Candesartan (Cilexetil); DSSTox_CID_239; Spectrum2_000485; Spectrum3_000996; Spectrum4_001124; Spectrum5_001462; DSSTox_RID_85567; DSSTox_GSID_20239; SCHEMBL40831; BSPBio_002691; KBioGR_001607; KBioSS_002187; 1H-Benzimidazolium, 7-carboxy-1-(2-((cyclohexylcarbonyl)oxy)ethyl)-2-ethoxy-1-(2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl)-, hydroxide, inner salt, (+-)-; Candesartan Cilexetil-[d11]; MLS004774127; Candesartan cilexetil , 97%; SPECTRUM1504261; SPBio_000349; GTPL8352; Candesartan cilexetil (Atacand); DTXSID5020239; KBio2_002187; KBio2_004755; KBio2_007323; KBio3_001911; EBD4212; HMS1922J09; HMS2093E20; HMS3651I08; Pharmakon1600-01504261; Candesartan cilexetil (JP17/USP); BCP22050; Tox21_302202; AC-204; BDBM50318907; CCG-39530; NSC758697; s2037; STL451065; AKOS015894954; AKOS015920180; AB07617; AM90293; BCP9000480; CCG-222334; DB00796; DS-1302; KS-1147; NSC 758697; NSC-758697; VA10473; Candesartan cilexetil, >=98% (HPLC); NCGC00095123-01; NCGC00095123-02; NCGC00095123-03; NCGC00095123-05; NCGC00095123-10; NCGC00095123-16; NCGC00255218-01; (+-)-1-Hydroxyethyl 2-ethoxy-1-(p-(o-1H-tetrazol-5-ylphenyl)benzyl)-7-benzimidazolecarboxylate, cyclohexyl carbonate (ester); 1-{[(cyclohexyloxy)carbonyl]oxy}ethyl 2-(ethyloxy)-1-{[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylate; 1H-Benzimidazole-7-carboxylic acid, 2-ethoxy-1-((2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl)methyl)-, 1-(((cyclohexyloxy)carbonyl)oxy)ethyl ester, (+-)-; AK-75900; HY-17505; SMR003500784; SBI-0206767.P001; AB0012012; C-265; CAS-145040-37-5; FT-0602914; SW220041-1; A-2005; C07709; D00626; J10436; AB01274805-01; AB01274805_02; AB01274805_03; 040C375; H212/91; L006257; SR-05000001976; Camptothecine, Antibiotic for Culture Media Use Only; Q-200786; SR-05000001976-1; BRD-A65671304-001-02-6; BRD-A65671304-001-03-4; Q27075664; Candesartan 1-(((cyclohexyloxy)carbonyl)oxy)ethyl ester; Candesartan cilexetil, European Pharmacopoeia (EP) Reference Standard; Candesartan cilexetil, United States Pharmacopeia (USP) Reference Standard; Candesartan cilexetil for peak identification, European Pharmacopoeia (EP) Reference Standard; Candesartan cilexetil for system suitability, European Pharmacopoeia (EP) Reference Standard; Candesartan Cilexetil, Pharmaceutical Secondary Standard; Certified Reference Material; (+/-)-1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[2'-(1H-tetrazol-5-yl) biphenyl-4-yl]methylbenzimidazole-7-carboxylate; (+/-)-1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methylbenzimidazole-7-carboxylate; 1-(Cyclohexyloxycarbonyloxy)ethyl-2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazol-7-carboxylate; 1-{[(cyclohexyloxy)carbonyl]oxy}ethyl 2-ethoxy-1-{[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylate; 1-cyclohexyloxycarbonyloxyethyl 2-ethoxy-3-[[4-[2-(2h-tetrazol-5-yl)phenyl]phenyl] methyl]benzimidazole-4-carboxylate; 1-cyclohexyloxycarbonyloxyethyl 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate.; 1H-Benzimidazole-7-carboxylic acid, 2-ethoxy-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-, 1-[[(cyclohexyloxy)carbonyl]oxy]ethyl ester; 2-Ethoxy-1-[2'-(1H-tetrazole-5-yl)-4-biphenylylmethyl]-1H-benzimidazole-7-carboxylic acid 1-(cyclohexyloxycarbonyloxy)ethyl ester; 2-Ethoxy-3-[2''-(1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid 1-cyclohexyloxycarbonyloxy-ethyl ester; 2-Ethoxy-3-[2''-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid 1-cyclohexyloxycarbonyloxy-ethyl ester; 2-ethoxy-3-[2'-(1h-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3h-benzoimidazole-4-carboxylic acid 1-cyclohe
Click to Show/Hide
|
|||
Molecular Type |
Small molecule
|
|||
Disease | Hypertension [ICD-11: BA00] | Approved | [1] | |
Structure |
![]() |
Click to Download Mol2D MOL |
||
Click to Show/Hide the Molecular Information and External Link(s) of This Natural Product | ||||
Formula |
C33H34N6O6
|
|||
PubChem CID | ||||
Canonical SMILES |
CCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)OC(C)OC(=O)OC6CCCCC6
|
|||
InChI |
1S/C33H34N6O6/c1-3-42-32-34-28-15-9-14-27(31(40)43-21(2)44-33(41)45-24-10-5-4-6-11-24)29(28)39(32)20-22-16-18-23(19-17-22)25-12-7-8-13-26(25)30-35-37-38-36-30/h7-9,12-19,21,24H,3-6,10-11,20H2,1-2H3,(H,35,36,37,38)
|
|||
InChIKey |
GHOSNRCGJFBJIB-UHFFFAOYSA-N
|
|||
CAS Number |
CAS 145040-37-5
|
|||
ChEBI ID | ||||
DrugBank ID |
Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally | ||||||
---|---|---|---|---|---|---|
α. A List of Natural Product(s) Able to Enhance the Efficacy of This Drug | ||||||
Trandolapril | Homo sapiens | Click to Show/Hide the Molecular Data of This NP | ||||
Achieving Therapeutic Synergy | Click to Show/Hide | |||||
Representative Experiment Reporting the Effect of This Combination | [2] | |||||
Detail(s) |
Combination Info
![]() |
|||||
In-vivo Model | Clinical trial | |||||
Experimental
Result(s) |
Combination therapy with trandolapril and candesartan cilexetil has an additive effect on the reduction of microalbuminuria in microalbuminuric normotensive type 2 diabetes patients. |
Target and Pathway | ||||
---|---|---|---|---|
Target(s) | Integrin alpha-V (ITGAV) | Molecule Info | [3] | |
Integrin beta-3 (ITGB3) | Molecule Info | [3] | ||
Integrin beta-5 (ITGB5) | Molecule Info | [3] | ||
KEGG Pathway | Rap1 signaling pathway | Click to Show/Hide | ||
2 | Phagosome | |||
3 | PI3K-Akt signaling pathway | |||
4 | Osteoclast differentiation | |||
5 | Focal adhesion | |||
6 | ECM-receptor interaction | |||
7 | Platelet activation | |||
8 | Hematopoietic cell lineage | |||
9 | Regulation of actin cytoskeleton | |||
10 | Thyroid hormone signaling pathway | |||
11 | Proteoglycans in cancer | |||
12 | MicroRNAs in cancer | |||
13 | Hypertrophic cardiomyopathy (HCM) | |||
14 | Arrhythmogenic right ventricular cardiomyopathy (ARVC) | |||
15 | Dilated cardiomyopathy | |||
16 | Cell adhesion molecules (CAMs) | |||
17 | Pathways in cancer | |||
18 | Small cell lung cancer | |||
NetPath Pathway | Leptin Signaling Pathway | Click to Show/Hide | ||
Panther Pathway | Integrin signalling pathway | Click to Show/Hide | ||
2 | CCKR signaling map ST | |||
Pathway Interaction Database | IL4-mediated signaling events | Click to Show/Hide | ||
2 | Integrin family cell surface interactions | |||
3 | Signaling events mediated by PTP1B | |||
4 | Beta3 integrin cell surface interactions | |||
5 | S1P3 pathway | |||
6 | Osteopontin-mediated events | |||
7 | Nectin adhesion pathway | |||
8 | Arf6 signaling events | |||
9 | S1P1 pathway | |||
10 | Integrins in angiogenesis | |||
11 | Urokinase-type plasminogen activator (uPA) and uPAR-mediated signaling | |||
12 | PDGFR-beta signaling pathway | |||
13 | Signaling events mediated by VEGFR1 and VEGFR2 | |||
14 | Ephrin B reverse signaling | |||
15 | Beta1 integrin cell surface interactions | |||
16 | Arf6 trafficking events | |||
17 | CXCR4-mediated signaling events | |||
18 | Plexin-D1 Signaling | |||
19 | PDGFR-alpha signaling pathway | |||
20 | Beta5 beta6 beta7 and beta8 integrin cell surface interactions | |||
21 | Signaling events mediated by focal adhesion kinase | |||
Reactome | Platelet degranulation | Click to Show/Hide | ||
2 | Elastic fibre formation | |||
3 | PECAM1 interactions | |||
4 | Molecules associated with elastic fibres | |||
5 | Integrin cell surface interactions | |||
6 | Syndecan interactions | |||
7 | ECM proteoglycans | |||
8 | Integrin alphaIIb beta3 signaling | |||
9 | GRB2:SOS provides linkage to MAPK signaling for Integrins | |||
10 | p130Cas linkage to MAPK signaling for integrins | |||
11 | VEGFA-VEGFR2 Pathway | |||
12 | MAP2K and MAPK activation | |||
13 | Cross-presentation of particulate exogenous antigens (phagosomes) | |||
14 | Laminin interactions | |||
WikiPathways | Monoamine Transport | Click to Show/Hide | ||
2 | TGF beta Signaling Pathway | |||
3 | Osteoblast Signaling | |||
4 | Focal Adhesion | |||
5 | Hematopoietic Stem Cell Differentiation | |||
6 | Human Complement System | |||
7 | Syndecan interactions | |||
8 | Extracellular matrix organization | |||
9 | Elastic fibre formation | |||
10 | Primary Focal Segmental Glomerulosclerosis FSGS | |||
11 | Arrhythmogenic Right Ventricular Cardiomyopathy | |||
12 | Integrin-mediated Cell Adhesion | |||
13 | L1CAM interactions | |||
14 | Integrin cell surface interactions | |||
15 | Integrin alphaIIb beta3 signaling | |||
16 | Cell surface interactions at the vascular wall | |||
17 | Serotonin Transporter Activity | |||
18 | Osteopontin Signaling | |||
19 | Osteoclast Signaling | |||
20 | Class I MHC mediated antigen processing & presentation |
