Indeglitazar - ≥98% , Peroxisome proliferator-activated receptor agonist, CAS No.835619-41-5, Peroxisome proliferator-activated receptor agonist

CAS: 835619-41-5 Cat. No.: I649701 Formule: C19H19NO6S Poids moléculaire: 389.42 PubChem CID: 11395145
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ ≥98%
Synonyms
Indeglitazar | MS-26475 | INDEGLITAZAR [INN] | Indeglitazar (USAN) | AKOS040741878 | Indeglitazar [USAN] | 3-[1-(4-Methoxy benzenesulfonyl)-5-methoxy-1H-indol-3-yl]-propionic acid | YMPALHOKRBVHOJ-UHFFFAOYSA-N | PLX-204 | HY-14817 | PPM 204 | Q27096942 |
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Taille
Allemagne (EU)
USA*
Prix
Qté
1mg
I649701-1mg
—
2 En stock

45,90€

69,33€
Enregistrer 23,43 € (33.79%)
5mg
I649701-5mg
—
2 En stock

169,12€

254,16€
Enregistrer 85,04 € (33.46%)
10mg
I649701-10mg
—
2 En stock

252,43€

379,12€
Enregistrer 126,69 € (33.42%)
25mg
I649701-25mg
—
1 En stock

429,44€

644,64€
Enregistrer 215,20 € (33.38%)
50mg
I649701-50mg
—
1 En stock

773,07€

1 160,08€
Enregistrer 387,01 € (33.36%)
100mg
I649701-100mg
—
1 En stock

1 391,77€

2 087,69€
Enregistrer 695,93 € (33.33%)
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Pourquoi cette qualité

≥98% pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Store at -20°C Expédition Ice chest + Ice pads. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 0 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Indeglitazar (PPM 204) is an orally available PPAR pan-agonist for all three PPARα , PPARδ and PPARγ

In Vitro

In an assay of preadipocyte differentiation, measuring in part functional insulin sensitization capability of the cells, Indeglitazar shows an EC 50 of 0.32 μM compared with Rosiglitazone, which shows an EC 50 of 13 nM, although the maximal response obtained from the 2 compounds is comparable. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

An initial assessment of in vivo activity is carried out using the Zucker rat model of diabetes. The significant lowering of glucose, HbA 1C , triglycerides, and total cholesterol are observed after i.v. treatment with 10 mg/kg Indeglitazar once per day for 3 weeks. Notably, the level of Adiponectin (on day 21) is essentially unchanged in treated vs. untreated animals (4.8 mcg/mL vs. 4.9 mcg/mL), thus the observed reductions in glucose and HbA 1C are achieved in an adiponectin-independent fashion. These differences in the effects of Indeglitazar in vivo may be a consequence of synergy between the 3 PPAR activities or because of the SPPARM profile of the compound, or a combination of these factors. The oral activity of Indeglitazar is assessed in the ob/ob model of diabetes and insulin resistance. Indeglitazar significantly decreases glucose, insulin, triglycerides, and free fatty acid levels . MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:PPARα PPARδ PPARγ

Spécifications

Synonymes
Indeglitazar | MS-26475 | INDEGLITAZAR [INN] | Indeglitazar (USAN) | AKOS040741878 | Indeglitazar [USAN] | 3-[1-(4-Methoxy benzenesulfonyl)-5-methoxy-1H-indol-3-yl]-propionic acid | YMPALHOKRBVHOJ-UHFFFAOYSA-N | PLX-204 | HY-14817 | PPM 204 | Q27096942 |
Spécifications et pureté
≥98%
Mécanismes biochimiques et physiologiques
Indeglitazar (PPM 204) is an orally available PPAR pan-agonist for all three PPARα , PPARδ and PPARγ.
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Type d'action
AGONIST
Mécanisme d'action
Peroxisome proliferator-activated receptor agonist
Pureté
≥98%
Propriétés du produit
ALogP
2.9
Noms et identifiants
Pubchem Sid
Sourires canoniques
COC1=CC=C(C=C1)S(=O)(=O)N2C=C(C3=C2C=CC(=C3)OC)CCC(=O)O
IUPAC Name
3-[5-methoxy-1-(4-methoxyphenyl)sulfonylindol-3-yl]propanoic acid
InChIKey
YMPALHOKRBVHOJ-UHFFFAOYSA-N
INCHI
1S/C19H19NO6S/c1-25-14-4-7-16(8-5-14)27(23,24)20-12-13(3-10-19(21)22)17-11-15(26-2)6-9-18(17)20/h4-9,11-12H,3,10H2,1-2H3,(H,21,22)
Isomères SMILES
COC1=CC=C(C=C1)S(=O)(=O)N2C=C(C3=C2C=CC(=C3)OC)CCC(=O)O
PubChem CID
11395145
Poids moléculaire
389.42

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseIndoles and derivatives
SubclassIndolyl carboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentIndolyl carboxylic acids and derivatives
Alternative Parents 3-alkylindoles  Benzenesulfonamides  Benzenesulfonyl compounds  Phenoxy compounds  Anisoles  Methoxybenzenes  Alkyl aryl ethers  Substituted pyrroles  Sulfonyls  Organosulfonic acids and derivatives  Heteroaromatic compounds  Monocarboxylic acids and derivatives  Azacyclic compounds  Carboxylic acids  Carbonyl compounds  Hydrocarbon derivatives  Organic oxides  Organonitrogen compounds  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indolyl carboxylic acid derivative - 3-alkylindole - Benzenesulfonamide - Benzenesulfonyl group - Indole - Methoxybenzene - Phenol ether - Anisole - Phenoxy compound - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Substituted pyrrole - Pyrrole - Heteroaromatic compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Ether - Azacycle - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. These are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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Analytical Chart:

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12 results found

Lot NumberCertificate TypeDateArticle
F2503383F2503383Certificate of AnalysisNov 02, 2024 I649701
F2503384F2503384Certificate of AnalysisNov 02, 2024 I649701
F2503385F2503385Certificate of AnalysisNov 02, 2024 I649701
F2503386F2503386Certificate of AnalysisNov 02, 2024 I649701
F2503387F2503387Certificate of AnalysisNov 02, 2024 I649701
F2503388F2503388Certificate of AnalysisNov 02, 2024 I649701
F2503389F2503389Certificate of AnalysisNov 02, 2024 I649701
F2503390F2503390Certificate of AnalysisNov 02, 2024 I649701
F2503391F2503391Certificate of AnalysisNov 02, 2024 I649701
F2503392F2503392Certificate of AnalysisNov 02, 2024 I649701
F2503393F2503393Certificate of AnalysisNov 02, 2024 I649701
F2503394F2503394Certificate of AnalysisNov 02, 2024 I649701
Propriétés chimiques et physiques
SolubilitéDMSO : 100 mg/mL (256.79 mM; Need ultrasonic)
Poids moléculaire389.400 g/mol
XLogP32.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass389.093 Da
Monoisotopic Mass389.093 Da
Topological Polar Surface Area103.000 Ų
Heavy Atom Count27
Formal Charge0
Complexity610.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculateurs de solution
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