Dencichine - Moligand™,≥98% , CAS No.5302-45-4

CAS: 5302-45-4 Cat. No.: D647788 Formule: C5H8N2O5 Poids moléculaire: 176.13 PubChem CID: 440259
DISPONIBLE À COMMANDE
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. ≥98%
Synonyms
N3-Oxalyl-L-2,3-diaminopropanoate | A13552 | 3-N-Oxalyl-L-2,3-diaminopropanoic acid | Dencichin | UNII-O8VT5BZ48B | beta-ODAP | N-Oxalyl-L-alpha-beta-diaminopropionic acid (BOAA,ODAP) | oxalyldiaminopropionic acid, (L-Ala)-isomer | beta-N-Oxalyl-L-alpha,b
Storage
Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
Size
USA
Allemagne (EU)*
Price
Qty
5mg
D647788-5mg
Sur commande · 8–12 semaines
88,90$US
10mg
D647788-10mg
Sur commande · 8–12 semaines
154,90$US
25mg
D647788-25mg
Sur commande · 8–12 semaines
329,90$US
50mg
D647788-50mg
Sur commande · 8–12 semaines
489,90$US
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™,≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Dencichin is a non-protein amino acid originally extracted from Panax notoginseng , and can inhibit HIF-prolyl hydroxylase-2 (PHD-2) activity.

In Vitro

Dencichin (β-ODAP, 10 μM, 50 μM, 100 μM and 200 μM) increases HRE expression by 1.3±0.09, 2.5±0.07, 4.2±0.15 and 1.3±0.07 fold respectively compared to control. Dencichin has intermolecular interactions with PHD-2. Dencichin (10 μM, 100 μM, 1 mM) significantly inhibits cell proliferation and extracellular matrix (ECM) proteins accumulation of HBZY-1 cells, and reduces the secretion of collagen I (Col I), collagen IV (Col IV), and fibronectin (FN). MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Dencichin improves metabolism disorder in diabetic nephropathy (DN) secondary to type II diabetes mellitus (DM) model. Dencichin (80, 160 mg/kg/day, p.o.) significantly prevents the up-regulation of TCH, TG, LDL, and HbAlc and the down-regulation of HDL in DN rats induced by STZ injection. Dencichin also attenuates renal injury induced in the DN secondary to type II DM model. Dencichin alleviates pancreas damage in the STZ-induced DN model. Dencichin regulates protein expression in the TGF-β/Smad signalling pathway in STZ-induced DN models. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Assay

Cells are cultured in 6-well plates with glucose (LG) or high glucose control (HG) and then treated with valsartan (1.0 × 10 -3 M) or Dencichin (1.0 × 10 -5 M, 1.0 × 10 -4 M and 1.0 × 10 -3 M) for 24 h before analysing the activation of FN, Col I, and Col IV expression by ELISA and analysing MMP-9 and TIMP-1 expression by immunofluorescence. Each experiment is repeated at least three times throughout the study. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal administration

Male SD rats weighted approximately 200 ± 20 g (eight weeks old) are kept at 23 ± 2°C. The rats are randomLy allotted into two groups: normal group (n = 16) and diabetic nephropathy (DN) group (n = 60). The normal rats fed with normal diet and vehicle fall into the normal control group (NC, n = 8) and the normal rats fed with normal diet and Dencichin fall into the Dencichin control group (De C, n = 8). The rats in the diabetic group are fed the high-sugar-high-fat diet (composition: Common breeding material 54.6%, lard oil 16.9%, sucrose 14%, casein 10.2%, gunk 2.1%, maltodextrin 2.2%). Five weeks later, DN is induced by administering of 40 mg/kg STZ though intraperitoneal injection, and the normal rats are treated with vehiclecitrate buffer (0.1 M, pH 4.2). Next, the DN rats (n = 32) are assigned into four groups and oral administered with metformin hydrochloride (a positive control) at 80 mg/kg/day, (DN+Met, n = 8), which is dissolve into distilled water to make a 2 mg/mL solution before use; vehicle control for the DN control group (DN, n = 8), or Dencichin. The Dencichin group is divided into a high Dencichin group ( 160 mg/kg/day ; DN+De H, n = 8) and a low Dencichin group ( 80 mg/kg/day ; DN+De L, n = 8), which are dissolved into distilled water to make a 5 mg/mL and 2.5 mg/mL solution before use and oral administered at the dosage once per day. Blood glucose is measured each month. 8 w after administering with Dencichin, the rats are killed . aladdin has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:PHD-2

Specifications

Synonymes
N3-Oxalyl-L-2,3-diaminopropanoate | A13552 | 3-N-Oxalyl-L-2,3-diaminopropanoic acid | Dencichin | UNII-O8VT5BZ48B | beta-ODAP | N-Oxalyl-L-alpha-beta-diaminopropionic acid (BOAA,ODAP) | oxalyldiaminopropionic acid, (L-Ala)-isomer | beta-N-Oxalyl-L-alpha,b
Spécifications et pureté
Moligand™,≥98%
Mécanismes biochimiques et physiologiques
Dencichin is a non-protein amino acid originally extracted from Panax notoginseng , and can inhibit HIF-prolyl hydroxylase-2 (PHD-2) activity.
Conditions de stockage de stockage
Store at 2-8°C,Protected from light,Argon charged
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade
Moligand™
Type d'action
INHIBITOR
Pureté
≥98%
Noms et identifiants
Pubchem Sid528769011
Sourires canoniquesC(C(C(=O)O)N)NC(=O)C(=O)O
IUPAC Name(2S)-2-amino-3-(oxaloamino)propanoic acid
InChIKeyNEEQFPMRODQIKX-REOHCLBHSA-N
INCHI1S/C5H8N2O5/c6-2(4(9)10)1-7-3(8)5(11)12/h2H,1,6H2,(H,7,8)(H,9,10)(H,11,12)/t2-/m0/s1
Isomères SMILES C([C@@H](C(=O)O)N)NC(=O)C(=O)O
CAS alternatif 5302-45-4
PubChem CID 440259
Termes d'entrée MeSH (2-amino-2-carboxymethyl)-L-oxamic acid;2-oxalylamino-3-aminopropionic acid;3-amino-N-(carboxycarbonyl)-DL-alanine;3-amino-N-(carboxycarbonyl)alanine;3-oxalylamino-2-aminopropionic acid;beta-N-oxalylamino-L-alanine;beta-N-oxalylaminoalanine;beta-N-oxalyla
Poids moléculaire 176.13

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
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Dicarboxylic acids and derivatives  Secondary carboxylic acid amides  Amino acids  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-alpha-amino acid - Dicarboxylic acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Amino acid - Carboxylic acid - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Amine - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors N(beta)-acyl-L-2,3-diaminopropionic acid
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDateArticle
A2604884Certificate of AnalysisNov 20, 2025 D647788
A2604888Certificate of AnalysisNov 20, 2025 D647788
A2604889Certificate of AnalysisNov 20, 2025 D647788
A2604890Certificate of AnalysisNov 20, 2025 D647788
Propriétés chimiques et physiques
SolubilitéDMSO : 5 mg/mL (28.39 mM; Need ultrasonic) H2O : 5 mg/mL (28.39 mM; Need ultrasonic)
Sensibilitélight sensitive;air sensitive
Poids moléculaire176.130 g/mol
XLogP3-4.100
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count4
Exact Mass176.043 Da
Monoisotopic Mass176.043 Da
Topological Polar Surface Area130.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity214.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Références
1. Jing Chen, Ying Yuan, Xiaoku Ran, Na Guo, Deqiang Dou.  (2018)  Metabolomics analysis based on a UPLC-Q-TOF-MS metabolomics approach to compare Lin-Xia-Shan-Shen and garden ginseng.  RSC Advances,  (53): (30616-30623).  [PMID:35546833] [10.1039/C8RA04823A]
Calculateurs de solution
Avis

Avis des clients

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.