PROTAC RAR Degrader-1 - ≥95% , CAS No.1351169-27-1

CAS: 1351169-27-1 Cat. No.: P648151 Peso molecular: 917.14 PubChem CID: 54764325
Disponible para pedir
GRADE & PURITY ≥95%
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
Application
PROTAC
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
P648151-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.100,90US$
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

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

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Quality documents

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

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Literature proof

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

Descripción general

PROTAC RAR Degrader-1 comprises a IAP ligand binding group, a linker and a RAR ligand binding group. PROTAC RAR Degrader-1 is an RAR degrader. Maximal RAR degradation at 30 μM concentration in HT1080 cells. Degradation inducers based on cIAP1 are called specific and non-genetic IAP-dependent protein erasers ( SNIPER s)

Form:Solid

IC50& Target:cIAP1

Specifications

Especificaciones y pureza
≥95%
Mecanismos bioquímicos y fisiológicos
PROTAC RAR Degrader-1 comprises a IAP ligand binding group, a linker and a RAR ligand binding group. PROTAC RAR Degrader-1 is an RAR degrader. Maximal RAR degradation at 30 μM concentration in HT1080 cells. Degradation inducers based on cIAP1 are called s
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicasCC(C)CC(C(=O)NCCOCCOCCOCC(=O)NCCCOC1=C(C=CC(=C1)C=CC(=O)C2=CC(=CC(=C2)C(C)(C)C)C(C)(C)C)C(=O)O)NC(=O)C(C(CC3=CC=CC=C3)N)O
IUPAC Name2-[3-[[2-[2-[2-[2-[[(2S)-2-[[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanoyl]amino]-4-methylpentanoyl]amino]ethoxy]ethoxy]ethoxy]acetyl]amino]propoxy]-4-[(E)-3-(3,5-ditert-butylphenyl)-3-oxoprop-1-enyl]benzoic acid
InChIKeyZAOSGDCLGNWLSI-ACALULJJSA-N
INCHI1S/C51H72N4O11/c1-34(2)27-42(55-48(60)46(58)41(52)28-35-13-10-9-11-14-35)47(59)54-20-22-63-23-24-64-25-26-65-33-45(57)53-19-12-21-66-44-29-36(15-17-40(44)49(61)62)16-18-43(56)37-30-38(50(3,4)5)32-39(31-37)51(6,7)8/h9-11,13-18,29-32,34,41-42,46,58H,12,19-28,33,52H2,1-8H3,(H,53,57)(H,54,59)(H,55,60)(H,61,62)/b18-16+/t41-,42+,46+/m1/s1
Isómeros SMILES CC(C)C[C@@H](C(=O)NCCOCCOCCOCC(=O)NCCCOC1=C(C=CC(=C1)/C=C/C(=O)C2=CC(=CC(=C2)C(C)(C)C)C(C)(C)C)C(=O)O)NC(=O)[C@H]([C@@H](CC3=CC=CC=C3)N)O
PubChem CID 54764325
Peso molecular 917.14

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.

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📊 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
ClasePeptidomimetics
SubclassHybrid peptides
Intermediate Tree Nodes Not available
Direct ParentHybrid peptides
Alternative Parents Retrochalcones  Leucine and derivatives  N-acyl-alpha amino acids and derivatives  Alpha amino acid amides  Beta amino acids and derivatives  Amphetamines and derivatives  Benzoic acids  Phenylpropanes  Phenol ethers  Phenoxy compounds  Styrenes  Aryl ketones  Benzoyl derivatives  Alkyl aryl ethers  Aralkylamines  N-acyl amines  Monosaccharides  Enones  Acryloyl compounds  Amino acids  Secondary carboxylic acid amides  Secondary alcohols  Monocarboxylic acids and derivatives  Dialkyl ethers  Carboxylic acids  Monoalkylamines  Hydrocarbon derivatives  Organopnictogen compounds  Organic oxides  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Hybrid peptide - Retrochalcone - Linear 1,3-diarylpropanoid - Leucine or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Beta amino acid or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Amphetamine or derivatives - Benzoic acid or derivatives - Benzoic acid - Phenylpropane - Phenoxy compound - Benzoyl - Phenol ether - Styrene - Aryl ketone - Alkyl aryl ether - Aralkylamine - Benzenoid - Monocyclic benzene moiety - N-acyl-amine - Monosaccharide - Fatty amide - Fatty acyl - Alpha,beta-unsaturated ketone - Acryloyl-group - Enone - Amino acid - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Secondary alcohol - Ketone - Dialkyl ether - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Carboxylic acid - Primary amine - Alcohol - Organic oxide - Hydrocarbon derivative - Organopnictogen compound - Carbonyl group - Amine - Organic oxygen compound - Primary aliphatic amine - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as hybrid peptides. These are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadDMSO : ≥ 80 mg/mL (87.23 mM)
Calculadoras de soluciones
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