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· · COA & SDS Disponible para cada producto · Envío el mismo día para artículos en stock Enfuvirtide , Transmembrane glycoprotein gp41 inhibitor, CAS No.16130199, Transmembrane glycoprotein gp41 inhibitor
Synonyms
Enfuvirtide | TNX-355 & Efuvirtide | DTXSID20166672 | AKOS040763974 | DP-178 | J05AX07 | Dp 178 | Humanized monoclonal antibody to CD4 & Ac-YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF-NH2 | DP178 | Enfuvirtide [USAN:INN:BAN] | AcTyrThrSerLeuIleHisSerLeuIleGluGlu
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Why this grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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
Enfuvirtide | TNX-355 & Efuvirtide | DTXSID20166672 | AKOS040763974 | DP-178 | J05AX07 | Dp 178 | Humanized monoclonal antibody to CD4 & Ac-YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF-NH2 | DP178 | Enfuvirtide [USAN:INN:BAN] | AcTyrThrSerLeuIleHisSerLeuIleGluGlu
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Transmembrane glycoprotein gp41 inhibitor
Propiedades del producto Nombres e identificadores Sonrisas canónicas
CCC(C)C(C(=O)NC(CCC(=O)O)C(=O)NC(CCC(=O)O)C(=O)NC(CO)C(=O)NC(CCC(=O)N)C(=O)NC(CC(=O)N)C(=O)NC(CCC(=O)N)C(=O)NC(CCC(=O)N)C(=O)NC(CCC(=O)O)C(=O)NC(CCCCN)C(=O)NC(CC(=O)N)C(=O)NC(CCC(=O)O)C(=O)NC(CCC(=O)N)C(=O)NC(CCC(=O)O)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC
IUPAC Name
(4S)-4-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S,3S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S,3S)-2-[[(2S)-2-[[(2S)-2-[[(2S,3R)-2-[[(2S)-2-acetamido-3-(4-hydroxyphenyl)propanoyl]amino]-3-hydroxybutanoyl]amino]-3-hydroxypropanoyl]amino
InChIKey
PEASPLKKXBYDKL-FXEVSJAOSA-N
INCHI
1S/C204H301N51O64/c1-20-102(15)166(253-195(310)137(75-100(11)12)239-200(315)150(93-258)251-190(305)143(82-112-90-215-95-219-112)248-203(318)167(103(16)21-2)254-196(311)138(76-101(13)14)240-201(316)151(94-259)252-204(319)168(105(18)260)255-197(312)13
Isómeros SMILES
CC[C@H](C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC3=CNC4=CC=CC=C43)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC5=CNC6=CC=CC=C65)C(=O)N[C@@H](CC7=CC=CC=C7)C(=O)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC8=CN=CN8)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CC9=CC=C(C=C9)O)NC(=O)C
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 Kingdom Organic compounds Superclass Organic Polymers Clase Polypeptides Subclass Not available Intermediate Tree Nodes Not available Direct Parent Polypeptides Alternative Parents Peptides Tyrosine and derivatives Phenylalanine and derivatives Histidine and derivatives Glutamic acid and derivatives Glutamine and derivatives Asparagine and derivatives Aspartic acid and derivatives Isoleucine and derivatives Leucine and derivatives N-acyl-alpha amino acids and derivatives Alpha amino acid amides Tryptamines and derivatives Serine and derivatives Alanine and derivatives Amphetamines and derivatives 3-alkylindoles 1-hydroxy-2-unsubstituted benzenoids N-acyl amines Substituted pyrroles Imidazoles Acetamides Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides Amino acids Primary carboxylic acid amides Carboxylic acids Azacyclic compounds Carbonyl compounds Organopnictogen compounds Monoalkylamines Organic oxides Hydrocarbon derivatives Primary alcohols Molecular Framework Aromatic heteropolycyclic compounds Substituents Polypeptide - Alpha peptide - Tyrosine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Glutamic acid or derivatives - Glutamine or derivatives - Leucine or derivatives - Isoleucine or derivatives - Aspartic acid or derivatives - Asparagine or derivatives - N-acyl-alpha amino acid or derivatives - Serine or derivatives - Triptan - Alpha-amino acid amide - Alanine or derivatives - 3-alkylindole - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Amphetamine or derivatives - Indole - Indole or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Fatty amide - N-acyl-amine - Substituted pyrrole - Fatty acyl - Benzenoid - Pyrrole - Acetamide - Heteroaromatic compound - Azole - Imidazole - Primary carboxylic acid amide - Amino acid or derivatives - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Amino acid - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Carbonyl group - Alcohol - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Amine - Primary alcohol - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues. External Descriptors polypeptide Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Peso molecular 4492.000 g/mol XLogP3 -14.700 Hydrogen Bond Donor Count 63 Hydrogen Bond Acceptor Count 67 Rotatable Bond Count 151 Exact Mass 4491.19 Da Monoisotopic Mass 4489.19 Da Topological Polar Surface Area 1900.000 Ų Heavy Atom Count 319 Formal Charge 0 Complexity 11200.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 39 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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