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Perindoprilat - Moligand™ , Inhibitor of Angiotensin-converting enzyme, CAS No.95153-31-4, Inhibitor of Angiotensin-converting enzyme

CAS: 95153-31-4 Cat. No.: P334937 分子式: C17H28N2O5 分子量: 340.41 EC番号: 110-978-1 PubChem CID: 72022
COA
Perindoprilat - Moligand™ CAS No(95153-31-4) by Aladdin Scientific
注文可能
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Synonyms
Discontinued. Please see P287531 or P287535 or P287585. | Q27088302 | ODAIHABQVKJNIY-PEDHHIEDSA-N | PERINDOPRILAT [INN] | Perindoprilate | Perindoprilatum (Latin) | X94 | (2S,3aS,7aS)-1-((2S)-2-(((1S)-1-carboxybutyl)amino)propanoyl)octahydro-1H-indole-2-c
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
USA
ドイツ (EU)*
Price
Qty
5mg
P334937-5mg
受注生産 · 8～12週間
$460.90
10mg
P334937-10mg
受注生産 · 8～12週間
$736.90
Enter a quantity for the sizes you want to add.
Bulk / Custom
♡ ウィッシュリスト ⇅ 比較リストに入れる ⎙ Print page
SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
概要 Specifications 製品の性質 名前と識別子 Documentation Advanced Data Taxonomic Classification 3 D構造 関連ターゲット（人間） 関連ターゲット（非人間） 作用メカニズム 証明書（CoA、COO、BSE/TSEと分析図） 化学的性質と物理的性質 ソリューション計算機 レビュー
🧪

Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

概要

Perindoprilat is an active metabolite of Perindopril , an ACE (angiotensin converting enzyme) inhibitor, which modulates the activity of low density lipoprotein receptor-related protein (LRP). LRP is a multifunctional endocytic receptor, which functions in the turnover of proteases and the degradation of extracellular matrix proteins. It is known that Perindoprilat inhibits the conversion of angiotensin I into angiotensin II, which lowers arteriolar pressure and increases venous capacity.

Specifications

同義語
Discontinued. Please see P287531 or P287535 or P287585. | Q27088302 | ODAIHABQVKJNIY-PEDHHIEDSA-N | PERINDOPRILAT [INN] | Perindoprilate | Perindoprilatum (Latin) | X94 | (2S,3aS,7aS)-1-((2S)-2-(((1S)-1-carboxybutyl)amino)propanoyl)octahydro-1H-indole-2-c
仕様と純度
Moligand™
保管条件
Store at -20°C
入荷
Ice chest + Ice pads
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
等級
Moligand™
アクションタイプ
INHIBITOR
作用メカニズム
Inhibitor of Angiotensin-converting enzyme
製品の性質
pKapKa: 2.27 (Predicted), pKa: 8.13 (Predicted)
名前と識別子
カノニカル・スマイルCCCC(C(=O)O)NC(C)C(=O)N1C2CCCCC2CC1C(=O)O
IUPAC Name(2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-carboxybutyl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid
InChIKeyODAIHABQVKJNIY-PEDHHIEDSA-N
INCHI1S/C17H28N2O5/c1-3-6-12(16(21)22)18-10(2)15(20)19-13-8-5-4-7-11(13)9-14(19)17(23)24/h10-14,18H,3-9H2,1-2H3,(H,21,22)(H,23,24)/t10-,11-,12-,13-,14-/m0/s1
異性体SMILES CCC[C@@H](C(=O)O)N[C@@H](C)C(=O)N1[C@H]2CCCC[C@H]2C[C@H]1C(=O)O
RTECS ND6007250
PubChem CID 72022
分子量 340.41

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
分類Carboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Peptides
Direct ParentDipeptides
Alternative Parents N-acyl-L-alpha-amino acids  Alpha amino acid amides  L-alpha-amino acids  Indoles and derivatives  Pyrrolidine carboxylic acids  N-acylpyrrolidines  Methyl-branched fatty acids  Heterocyclic fatty acids  Dicarboxylic acids and derivatives  Tertiary carboxylic acid amides  Amino acids  Dialkylamines  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  Carbonyl compounds  Organic oxides  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Alpha-dipeptide - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - N-acyl-l-alpha-amino acid - Alpha-amino acid amide - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Indole or derivatives - N-acylpyrrolidine - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Branched fatty acid - Heterocyclic fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Dicarboxylic acid or derivatives - Pyrrolidine - Tertiary carboxylic acid amide - Amino acid - Carboxamide group - Amino acid or derivatives - Azacycle - Carboxylic acid - Secondary aliphatic amine - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organopnictogen compound - Amine - Organooxygen compound - Organonitrogen compound - Aliphatic heteropolycyclic compound
説明This compound belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
External Descriptors Not available
3 D構造
インタラクティブ化学構造モデル





関連ターゲット（人間）
ACE Tclin Angiotensin-converting enzyme (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
関連ターゲット（非人間）
Abcb1b P-glycoprotein 1 (174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
作用メカニズム
証明書（CoA、COO、BSE/TSEと分析図）
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
化学的性質と物理的性質
溶解度Soluble in ethanol, methanol, and water.
屈折率n20D1.54 (Predicted)
沸点（°C）~568.1° C at 760 mmHg (Predicted)
融点（°C）136-140° C
分子量340.400 g/mol
XLogP30.200
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass340.2 Da
Monoisotopic Mass340.2 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity495.000
Isotope Atom Count0
Defined Atom Stereocenter Count5
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
ソリューション計算機
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