AUDA - ≥98% , CAS No.479413-70-2

CAS: 479413-70-2 Cat. No.: A346203 Peso molecular: 392.58
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
12-[[(tricyclo[3.3.1.13,7]dec-1-ylamino)carbonyl]amino]-dodecanoic acid | HY-108570 | S0752 | MFCD12912267 | 12-(3-adamantan-1-yl-ureido)-dodecanoic acid | 12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid | AUDA, >=98% (HPLC) | pyrene carboxaldehyde | A
Storage
Conservar a -20°C
Shipped In
Hielera + almohadillas de hielo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
10mg
A346203-10mg
3

36,90US$

55,90US$
Guardar 19,00 US$ (33.99%)
50mg
A346203-50mg
2

134,90US$

202,90US$
Guardar 68,00 US$ (33.51%)
250mg
A346203-250mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

505,90US$

758,90US$
Guardar 253,00 US$ (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Conservar a -20°C Ships Hielera + almohadillas de hielo 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.

Descripción general

El AUDA es un inhibidor de la epóxido hidrolasa soluble (sEH, IC|50|= 18 nM en ratones). Se ha demostrado que el AUDA tiene efectos hipotensores, acompañados de un aumento de la relación epóxido-diol en la orina. A una concentración de 10 μM, AUDA es capaz de activar el receptor α activado por proliferadores de peroxisomas (PPARα) 3 veces, mientras que no muestra capacidad para afectar a PPARδ o PPARγ.

Specifications

Sinónimos
12-[[(tricyclo[3.3.1.13, 7]dec-1-ylamino)carbonyl]amino]-dodecanoic acid | HY-108570 | S0752 | MFCD12912267 | 12-(3-adamantan-1-yl-ureido)-dodecanoic acid | 12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid | AUDA, >=98% (HPLC) | pyrene carboxaldehyde | A
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Pureza
≥98%
Propiedades del producto
pKapKa: 4.78 (Predicted)
Nombres e identificadores
Pubchem Sid504765228
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504765228
Sonrisas canónicasC1C2CC3CC1CC(C2)(C3)NC(=O)NCCCCCCCCCCCC(=O)O
IUPAC Name12-(1-adamantylcarbamoylamino)dodecanoic acid
InChIKeyXLGSEOAVLVTJDH-UHFFFAOYSA-N
INCHI1S/C23H40N2O3/c26-21(27)10-8-6-4-2-1-3-5-7-9-11-24-22(28)25-23-15-18-12-19(16-23)14-20(13-18)17-23/h18-20H,1-17H2,(H,26,27)(H2,24,25,28)
Isómeros SMILES C1C2CC3CC1CC(C2)(C3)NC(=O)NCCCCCCCCCCCC(=O)O
Peso molecular 392.58
Reaxy-Rn 9593536
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9593536&ln=

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
SuperclassLipids and lipid-like molecules
ClaseFatty Acyls
SubclassFatty acids and conjugates
Intermediate Tree Nodes Not available
Direct ParentMedium-chain fatty acids
Alternative Parents Amino fatty acids  Ureas  Monocarboxylic acids and derivatives  Carboxylic acids  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic homopolycyclic compounds
Substituents Medium-chain fatty acid - Amino fatty acid - Urea - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
EPHX2 Tchem Bifunctional epoxide hydrolase 2 (27 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALOX5 Tclin Arachidonate 5-lipoxygenase (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EPHX1 Tchem Epoxide hydrolase 1 (644 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CES2 Tchem Carboxylesterase 2 (583 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMPD1 Tchem Sphingomyelin phosphodiesterase (13561 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CES1 Tchem Acyl coenzyme A:cholesterol acyltransferase (1029 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EPHX2 Tchem Epoxide hydratase (3844 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ephx2 Epoxide hydrolase 2 (342 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsome (341 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

3 results found

Lot NumberCertificate TypeFechaArticulo
C2226376Certificate of AnalysisJan 08, 2025 A346203
C2226391Certificate of AnalysisJan 08, 2025 A346203
C2226455Certificate of AnalysisJan 08, 2025 A346203
Propiedades químicas y físicas
SolubilidadSoluble in water (0.5 mg/ml at 25° C), 100% ethanol (4 mg/ml), DMSO (≥ 10 mg/ml at 60° C), DMF (~2 mg/ml), and DMF : PBS (pH 7.2) (1:1) (~0.5 mg/ml).Soluble in DMSO
Índice de refracciónn20D1.53 (Predicted)
Punto de ebullición (°C)~592.7° C at 760 mmHg (Predicted)
Punto de fusión (°C)228.39° C (Predicted)
Peso molecular392.600 g/mol
XLogP35.900
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count3
Rotatable Bond Count13
Exact Mass392.304 Da
Monoisotopic Mass392.304 Da
Topological Polar Surface Area78.400 Ų
Heavy Atom Count28
Formal Charge0
Complexity479.000
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
Calculadoras de soluciones
Reseñas

Reseñas de cliente

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.