for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| ALogP | -1.1 |
|---|
| Canonical Smiles | C=C(CCCCCCCCCCCCCCCC1=NNN=N1)NS(=O)(=O)CCCC(=O)NCCOCCOCC(=O)NC(CCC(=O)NC(CCC(=O)NCCOCCOCC(=O)NC(CCCCNC(=O)CSCC(C(=O)O)N)C(=O)N)C(=O)O)C(=O)O |
|---|---|
| IUPAC Name | (2S)-5-[2-[2-[2-[[(2S)-1-amino-6-[[2-[(2R)-2-amino-2-carboxyethyl]sulfanylacetyl]amino]-1-oxohexan-2-yl]amino]-2-oxoethoxy]ethoxy]ethylamino]-2-[[(4S)-4-carboxy-4-[[2-[2-[2-[4-[17-(2H-tetrazol-5-yl)heptadec-1-en-2-ylsulfamoyl]butanoylamino]ethoxy]ethoxy]a |
| InChIKey | NAKSIOUBFDBTSW-ITMZJIMRSA-N |
| INCHI | 1S/C55H97N13O19S2/c1-40(18-13-11-9-7-5-3-2-4-6-8-10-12-14-20-45-64-67-68-65-45)66-89(82,83)35-17-21-46(69)59-27-29-84-32-34-87-37-50(73)63-44(55(80)81)23-25-48(71)62-43(54(78)79)22-24-47(70)60-28-30-85-31-33-86-36-49(72)61-42(52(57)75)19-15-16-26-58 |
| Isomeric SMILES | C=C(CCCCCCCCCCCCCCCC1=NNN=N1)NS(=O)(=O)CCCC(=O)NCCOCCOCC(=O)N[C@@H](CCC(=O)N[C@@H](CCC(=O)NCCOCCOCC(=O)N[C@@H](CCCCNC(=O)CSC[C@@H](C(=O)O)N)C(=O)N)C(=O)O)C(=O)O |
| PubChem CID | 122197536 |
| Molecular Weight | 1308.6 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Peptides |
| Direct Parent | Dipeptides |
| Alternative Parents | Gamma-glutamyl amino acids Glutamine and derivatives N-acyl-L-alpha-amino acids L-cysteine-S-conjugates L-alpha-amino acids Tricarboxylic acids and derivatives Organosulfonamides Organic sulfonamides N-acyl amines Tetrazoles Aminosulfonyl compounds Heteroaromatic compounds Amino acids Secondary carboxylic acid amides Primary carboxylic acid amides Sulfenyl compounds Azacyclic compounds Carboxylic acids Dialkyl ethers Dialkylthioethers Carbonyl compounds Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Alpha-dipeptide - Gamma-glutamyl alpha-amino acid - Glutamine or derivatives - L-cysteine-s-conjugate - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-l-alpha-amino acid - Cysteine or derivatives - Alpha-amino acid - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Tricarboxylic acid or derivatives - Fatty amide - N-acyl-amine - Organic sulfonic acid amide - Organosulfonic acid amide - Fatty acyl - Aminosulfonyl compound - Heteroaromatic compound - Azole - Tetrazole - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Amino acid or derivatives - Carboxamide group - Amino acid - Primary carboxylic acid amide - Secondary carboxylic acid amide - Sulfenyl compound - Dialkylthioether - Thioether - Azacycle - Organoheterocyclic compound - Carboxylic acid - Dialkyl ether - Ether - Organopnictogen compound - Organic nitrogen compound - Organic oxide - Primary aliphatic amine - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Primary amine - Organooxygen compound - Organosulfur compound - Amine - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. |
| External Descriptors | Not available |
