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Trandolapril

CAS No.
87679-37-6
Chemical Name:
Trandolapril
Synonyms
Mavik;Odrik;Odric;Udrik;Gopten;Preran;ru44570;Trantowa;Olivetolic;Ccris 6594
CBNumber:
CB8682356
Molecular Formula:
C24H34N2O5
Molecular Weight:
430.54
MDL Number:
MFCD00865776
MOL File:
87679-37-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-03 11:24:09
Product description Number Pack Size Price
Trandolapril European Pharmacopoeia (EP) Reference Standard Y0000501 10 mg $127
Trandolapril ≥98% (HPLC), white powder T4827 10mg $196
Trandolapril pharmaceutical secondary standard, certified reference material PHR3146 250MG $222
Trandolapril British Pharmacopoeia (BP) Reference Standard BP1089 200MG $258
Trandolapril United States Pharmacopeia (USP) Reference Standard 1672687 125mg $435
More product size

Trandolapril Properties

Melting point 122-123°C
Boiling point 626.0±55.0 °C(Predicted)
Density 1.181±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO: ≥20mg/mL
form white powder
pka 3.15±0.20(Predicted)
color White to Off-White
InChIKey VXFJYXUZANRPDJ-WTNASJBWSA-N
SMILES N1(C(=O)[C@@H](N[C@H](C(OCC)=O)CCC2=CC=CC=C2)C)[C@]2([H])[C@]([H])(CCCC2)C[C@H]1C(O)=O
CAS DataBase Reference 87679-37-6(CAS DataBase Reference)
FDA UNII 1T0N3G9CRC
ATC code C09AA10
UNSPSC Code 41116107
NACRES NA.77

Pharmacokinetic data

Protein binding >80 (as trandolaprilat)
Excreted unchanged in urine 10-15%
Volume of distribution 18 Litres
Biological half-life 16-24 / - (as trandolaprilat)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)
GHS08
Signal word  Danger
Hazard statements  H360D
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
PPE Eyeshields, Gloves, type N95 (US)
WGK Germany  3
RTECS  NL6015178
HS Code  2933995300
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Repr. 1B
Hazardous Substances Data 87679-37-6(Hazardous Substances Data)
NFPA 704
0
3 0

Trandolapril price More Price(56)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000501 Trandolapril European Pharmacopoeia (EP) Reference Standard 87679-37-6 10 mg $127 2026-04-30 Buy
Sigma-Aldrich T4827 Trandolapril ≥98% (HPLC), white powder 87679-37-6 10mg $196 2026-04-30 Buy
Sigma-Aldrich PHR3146 Trandolapril pharmaceutical secondary standard, certified reference material 87679-37-6 250MG $222 2026-04-30 Buy
Sigma-Aldrich BP1089 Trandolapril British Pharmacopoeia (BP) Reference Standard 87679-37-6 200MG $258 2026-04-30 Buy
Sigma-Aldrich 1672687 Trandolapril United States Pharmacopeia (USP) Reference Standard 87679-37-6 125mg $435 2026-04-30 Buy
Product number Packaging Price Buy
Y0000501 10 mg $127 Buy
T4827 10mg $196 Buy
PHR3146 250MG $222 Buy
BP1089 200MG $258 Buy
1672687 125mg $435 Buy

Trandolapril Chemical Properties,Uses,Production

Description

Trandolapril is a new ACE inhibitor that is rapidly hydrolyzed, mainly in the liver, to its biologically active form, trandolaprilat. Compared with all other ACE inhibitors, trandolaprilat is reported to have the highest lipophilicity and the most prolonged ACE inhibitory activity. In hypertensive patients, trandolapril at a dose of 2 mg reduces blood pressure consistently throughout the 24 hour period after intake, making it one of the best once a day antihypertensive drugs. It has also been demonstrated to inhibit aortic atherosclerosis in the hyperlipidemic rabbit.

Chemical Properties

White or almost white powder.

Originator

Roussel Uclaf (France)

Uses

Trandolapril has been used as an angiotensin-converting enzyme (ACE) inhibitor to study its effects on responsiveness of human retinal endothelial cells (HRECs) to vascular endothelial growth factor (VEGF).

Uses

An antihypertensive. Angiotensin converting enzyme (ACE) inhibitor

Uses

antibacterial

Definition

ChEBI: Trandolapril is a heterobicylic compound that is (2S,3aR,7aS)-1-[(2S)-2-aminopropanoyl]octahydro-1H-indole-2-carboxylic acid in which the hydrogen of the amino group is substituted by a (2R)-1-ethoxy-1-oxo-4-phenylbutan-2-yl group. It is a angiotensin-converting enzyme inhibitor and a prodrug used for the treatment of hypertension. It has a role as a prodrug, an antihypertensive agent and an EC 3.4.15.1 (peptidyl-dipeptidase A) inhibitor. It is a dicarboxylic acid monoester, a dipeptide, an ethyl ester, a secondary amino compound, a tertiary carboxamide and an organic heterobicyclic compound. It is functionally related to a trandolaprilat.

brand name

Odrik; Udrik; Gopten

General Description

Trandolapril, 1-[2-(1-ethoxycarbonyl-3-phenylpropylamino)propionyl]octahydroindole-2-carboxylicacid (Mavik), is an indole-containing ACE inhibitorthat is structurally related to most of the precedingagents discussed. Enalapril is very similar to trandolapril,with the primary difference occurring in the heterocyclicsystems. The pyrrolidine of enalapril has been replacedwith an octahydroindole system. Much like enalaprilate,trandolapril must be hydrolyzed to tranolaprilate, which isthe bioactive species.

Biochem/physiol Actions

Trandolapril is an ACE inhibitor. Trandolapril differs from other ACE inhibitors in that it has a longer biological half-life and a high degree of lipophilicity.

Clinical Use

Angiotensin converting enzyme inhibitor:
Hypertension
Heat failure
After myocardial infarction

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Analgesics: antagonism of hypotensive effect and increased risk of renal impairment with NSAIDs; hyperkalaemia with ketorolac and other NSAIDs.
Antihypertensives: increased risk of hyperkalaemia, hypotension and renal failure with ARBs and aliskiren.
Bee venom extract: possible severe anaphylactoid reactions when used together.
Ciclosporin: increased risk of hyperkalaemia and nephrotoxicity.
Cytotoxics: increased risk of angioedema with everolimus.
Diuretics: enhanced hypotensive effect; hyperkalaemia with potassium-sparing diuretics.
ESAs: increased risk of hyperkalaemia; antagonism of hypotensive effect.
Gold: flushing and hypotension with sodium aurothiomalate.
Lithium: reduced excretion (possibility of enhanced lithium toxicity).
Potassium salts: increased risk of hyperkalaemia.
Tacrolimus: increased risk of hyperkalaemia and nephrotoxicity.

Metabolism

Trandolapril is metabolised in the liver to the active trandolaprilat and to some inactive metabolites. About 33
% of an oral dose of trandolapril is excreted in the urine, mainly as trandolaprilat; the rest is excreted in the faeces.

Trandolapril Preparation Products And Raw materials

Global( 238)Suppliers
Supplier Tel Email Country ProdList Advantage
Accendatech Co., Ltd.
+8613132578992 yunhao.liu@accendatech.com China 251 58
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055 Sibel@chuanghaibio.com China 8738 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21587 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29815 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
Antai Fine Chemical Technology Co.,Limited
18503026267 info@antaichem.com CHINA 9636 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32466 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9996 58
RongNa Biotechnology Co.,Ltd
+86-86-13583358881 +8618560316533 Brad@rongnabiotech.com China 3364 58

Related articles

View Lastest Price from Trandolapril manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Trandolapril pictures 2026-06-06 Trandolapril
87679-37-6
0.99 RongNa Biotechnology Co.,Ltd
Trandolapril pictures 2026-06-02 Trandolapril
87679-37-6
$39.00-115.00 99.70% 10g TargetMol Chemicals Inc.
Trandolapril pictures 2026-03-20 Trandolapril
87679-37-6
$10.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
  • Trandolapril pictures
  • Trandolapril
    87679-37-6
  • $39.00-115.00
  • 99.70%
  • TargetMol Chemicals Inc.
  • Trandolapril pictures
  • Trandolapril
    87679-37-6
  • $10.00
  • 99%
  • Hebei Chuanghai Biotechnology Co., Ltd

Trandolapril Spectrum

(2s-(1(r*(r*)),2-alpha,3a-alpha,7a-beta))-)amino)-1-oxopropyl) ru44570 (2s,3ar,7as)-1-[(2s)-2-[[(1s)-1-ethoxycarbonyl-3-phenyl-propyl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid Mavik, (2S,3aR,7aS)-1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]octahydro-1H-Indole-2-carboxylic acid (3αR.7αS)-1-[N-[1(S)-(Ethoxycarbonyl)-3-phenylpropy]-(S)-alanyl]oetahydroindole-2(S)-carboxylic acid TrandolaprilC24H34N205 Mavik, Odrik, Gopten, RU-44570 1H-Indole-2-carboxylic acid, 1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]octahydro-, (2S,3aR,7aS)- (9CI) 1H-Indole-2-carboxylic acid, 1-[2-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]octahydro-, [2S-[1[R*(R*)],2a,3aa,7ab]]- Gopten Odrik Trandolapril/(2S,3aR,7aS)-1-[(2S)-2-[[(1S)-1-Ethoxycarbonyl-3-phenyl-propyl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid (2S,3aR,7aS)-1-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]octahydro-1H-Indole-2-carboxylic Acid Mavik TRANDOLAPRIL Olivetolic 1H-Indole-2-carboxylic acid, octahydro-1-(2-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-1- oxopropyl)-, (2S-(1(R*(R*)),2-alpha,3a-alpha,7a-beta)) (2S,3aR,7aS)-1-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]propionyl]-3a,4,5,6,7,7a-hexahydro-2-indolinecarboxylic acid (2S,3aR,7aS)-1-[(S)-N-[(S)-1-Ethoxycarbonyl-3-phenylpropyl]alanyl]octahydro-1H-indole-2-carboxylic acid Odric Trantowa (2S,3Ar,7as)-1-((S)-N-((S)-1-carboxy-3-phenylpropyl)alanyl)hexahydro-2-indolinecarboxylic acid, 1-ethyl ester 1H-Indole-2-carboxylic acid, 1-((2S)-2-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-1-oxopropyl)octahydro-, (2S,3ar,7as)- Ccris 6594 Trandolapril (125 mg) (2S,3aR,7aS)-1-[(2S)-2-{[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]aMino}propanoyl]-octahydro-1H-indole-2-carboxylic acid Preran Tarka(coMb. with verapaMil) Udrik (2S,3aR,7aS)- 1H-Indole-2-carboxylicacid,1-[(2S)-2-[[(1S)- (2S,3aR,7aS)-1-((S)-2-(((S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl)aMino)propanoyl)octahydro-1H-indole-2-carboxylic acid 1H-Indole-2-carboxylicacid,1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]aMino]-1-oxopropyl]octahydro-,(2S,3aR,7aS)- Trandolapril Ph. Eur. (2S,3aR,7aS)-1-[(2S)-2-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid Trandolapril Solution, 1000ppm Trandolapril Solution, 100ppm Trandolapril CRS Trandolapril USP/EP/BP Trandolapril (RU44570) Trandolapril D6 TrandolaprilQ: What is Trandolapril Q: What is the CAS Number of Trandolapril Q: What is the storage condition of Trandolapril Q: What are the applications of Trandolapril Trandolapril (1672687) RU-44570,collagen,UUD model,inhibit,arterial hypertrophy,congestive heart failure,cellular fibronectin accumulation,Angiotensin-converting Enzyme (ACE),hypertension,CHF,RU 44570,spontaneously hypertensive rats,RU44570,Trandolapril,Inhibitor,UUO model,orally active,nonsulfhydryl,myocardial infarction,unilateral ureteral obstruction,Trandolaprilat Trandopril Trandolapril, 10 mM in DMSO 87679-37-6 TERRAMYCIN API Intermediates & Fine Chemicals Pharmaceuticals