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 | -10.9 |
|---|
| Canonical Smiles | CC(C)CC1C(=O)NC(CSSCC(NC(=O)CNC(=O)C(NC(=O)C(CSSCC(C(=O)NC(C(=O)N1)CCC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CC(=O)O)NC(=O)C(CC(=O)N)N)NC(=O)C(C)NC(=O)C(C(C)C)NC(=O)C(CC(=O)N)N)C(C)O)C(=O)NC(CC(C)C)C(=O)O)C(=O)NC(C(C)C)C(=O)O |
|---|---|
| IUPAC Name | (2R)-2-[[(4R,10S,13R,18R,21S,24S,27R)-18-[[(2S)-4-carboxy-2-[[(2S)-3-carboxy-2-[[(2R)-2,4-diamino-4-oxobutanoyl]amino]propanoyl]amino]butanoyl]amino]-21-(2-carboxyethyl)-27-[[(1S)-1-carboxy-2-methylpropyl]carbamoyl]-13-[[(2S)-2-[[(2S)-2-[[(2S)-2,4-diamino |
| InChIKey | WGEWYYPHYMGJNT-HLHYUOOASA-N |
| INCHI | 1S/C65H106N18O27S4/c1-25(2)15-35-56(99)80-41(60(103)82-49(28(7)8)65(109)110)24-114-111-21-38(58(101)77-37(64(107)108)16-26(3)4)72-44(87)20-70-62(105)50(30(10)84)83-61(104)40(78-51(94)29(9)71-63(106)48(27(5)6)81-53(96)32(67)18-43(69)86)23-113-112-22- |
| Isomeric SMILES | C[C@H]([C@H]1C(=O)NCC(=O)N[C@@H](CSSC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CSSC[C@@H](C(=O)N1)NC(=O)[C@H](C)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(=O)N)N)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](CC(=O)N)N)CCC(=O)O)CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)O)C(=O)N[C@H](CC(C)C)C(=O)O)O |
| PubChem CID | 118753634 |
| Molecular Weight | 1699.9 |
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 | Oligopeptides |
| Alternative Parents | Cyclic peptides Pentacarboxylic acids and derivatives Glutamic acid and derivatives Aspartic acid and derivatives Asparagine and derivatives Leucine and derivatives N-acyl-L-alpha-amino acids Macrolactams Valine and derivatives Alpha amino acid amides Alanine and derivatives N-acyl amines Organic disulfides Amino acids Lactams Secondary carboxylic acid amides Secondary alcohols Primary carboxylic acid amides Carboxylic acids Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Alpha-oligopeptide - Cyclic alpha peptide - Pentacarboxylic acid or derivatives - Glutamic acid or derivatives - Leucine or derivatives - Aspartic acid or derivatives - Asparagine or derivatives - Valine or derivatives - Macrolactam - N-acyl-l-alpha-amino acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alanine or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - N-acyl-amine - Fatty acyl - Fatty amide - Primary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Amino acid - Organic disulfide - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Carboxylic acid - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Primary aliphatic amine - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Alcohol - Carbonyl group - Primary amine - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. |
| External Descriptors | Not available |
