cyclo[Ala-Cys(1)-Ser-Ala-D-Pro-Dab-Arg-Tyr-Cys(1)-Tyr-Gln-Lys-D-Pro-Pro-Tyr-His] , C-X-C chemokine receptor type 4 antagonist, CAS No.162677492, C-X-C chemokine receptor type 4 antagonist

CAS: 162677492 Cat. No.: C671374 Peso molecular: 1864.1 PubChem CID: 162677492
Disponible para pedir
Synonyms
CHEMBL4802129
Storage
Room temperature
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Size
Estado
Price
Qty
1mg
C671374-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
999,90US$
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Why this grade

for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships 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.

Specifications

Sinónimos
CHEMBL4802129
Condiciones de almacenamiento de almacenamiento
Room temperature
Tipo de acción
ANTAGONIST
Mecanismo de acción
C-X-C chemokine receptor type 4 antagonist
Propiedades del producto
ALogP-3.6
Nombres e identificadores
Sonrisas canónicasCC1C(=O)NC2CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N4CCCC4C(=O)NC(C(=O)NC(C(=O)N1)CC5=CNC=N5)CC6=CC=C(C=C6)O)CCCCN)CCC(=O)N)CC7=CC=C(C=C7)O)NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C8CCCN8C(=O)C(NC(=O)C(NC2=O)CO)C)CCN)CCCNC(=N)N)CC9=CC=C(C=C9)O
IUPAC Name3-[(1R,4S,7S,10S,16R,22S,25S,28S,31S,34R,37S,40S,46R,49S,52S,55S)-10-(4-aminobutyl)-49-(2-aminoethyl)-52-(3-carbamimidamidopropyl)-37-(hydroxymethyl)-4,25,55-tris[(4-hydroxyphenyl)methyl]-28-(1H-imidazol-4-ylmethyl)-31,40-dimethyl-2,5,8,11,17,23,26,29,32,
InChIKeyMKXOUIKTXREBLX-NDKBASPVSA-N
INCHI1S/C84H118N24O21S2/c1-44-68(114)104-62-41-130-131-42-63(105-75(121)58(36-47-16-22-51(111)23-17-47)99-69(115)53(10-5-31-91-84(88)89)95-71(117)55(28-30-86)97-79(125)64-11-6-32-106(64)81(127)45(2)94-76(122)61(40-109)103-78(62)124)77(123)100-57(35-46-14
Isómeros SMILES C[C@H]1C(=O)N[C@H]2CSSC[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N3CCC[C@@H]3C(=O)N4CCC[C@H]4C(=O)N[C@H](C(=O)N[C@H](C(=O)N1)CC5=CNC=N5)CC6=CC=C(C=C6)O)CCCCN)CCC(=O)N)CC7=CC=C(C=C7)O)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H]8CCCN8C(=O)[C@@H](NC(=O)[C@@H](NC2=O)CO)C)CCN)CCCNC(=N)N)CC9=CC=C(C=C9)O
PubChem CID 162677492
Peso molecular 1864.1

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
ClasePeptidomimetics
SubclassHybrid peptides
Intermediate Tree Nodes Not available
Direct ParentHybrid peptides
Alternative Parents Arginine and derivatives  Glutamine and derivatives  N-acyl-alpha amino acids and derivatives  Serine and derivatives  Cysteine and derivatives  Alpha amino acid amides  Alanine and derivatives  Pyrrolidinecarboxamides  N-acylpyrrolidines  1-hydroxy-2-unsubstituted benzenoids  N-acyl amines  Benzene and substituted derivatives  Tertiary carboxylic acid amides  Imidazoles  Heteroaromatic compounds  Lactams  Guanidines  Dialkyldisulfides  Sulfenyl compounds  Carboximidamides  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Monoalkylamines  Imines  Hydrocarbon derivatives  Alcohols and polyols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Hybrid peptide - Arginine or derivatives - Glutamine or derivatives - N-acyl-alpha amino acid or derivatives - Serine or derivatives - Cysteine or derivatives - Alpha-amino acid amide - Alanine or derivatives - Alpha-amino acid or derivatives - N-substituted-alpha-amino acid - Pyrrolidine-2-carboxamide - Pyrrolidine carboxylic acid or derivatives - N-acylpyrrolidine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Fatty acyl - Benzenoid - N-acyl-amine - Fatty amide - Monocyclic benzene moiety - Heteroaromatic compound - Tertiary carboxylic acid amide - Pyrrolidine - Imidazole - Azole - Dialkyldisulfide - Organic disulfide - Lactam - Guanidine - Carboxamide group - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Carboximidamide - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Imine - Alcohol - Aromatic heteropolycyclic 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





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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