Moligand™ Moligand™ 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.
| Kanonisches Lächeln | COc1cccc2c1C(=O)c1c(O)c3[C@@H](O)C[C@](Cc3c(c1C2=O)O)(O)C(=O)CSC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N |
|---|---|
| IUPAC Name | (2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-1-oxo-3-[2-oxo-2-[(2S,4S)-2,4,5,12-tetrahydroxy-7-methoxy-6,11-dioxo-3,4-dihydro-1H-tetracen-2-yl]ethyl]sulfanylpropan-2-yl]amino]-5-oxopentanoic acid |
| InChIKey | LZWDZFWNTFSAGM-PGODJVSRSA-N |
| INCHI | 1S/C31H33N3O14S/c1-48-17-4-2-3-12-22(17)28(43)24-23(25(12)40)26(41)13-7-31(47,8-16(35)21(13)27(24)42)18(36)11-49-10-15(29(44)33-9-20(38)39)34-19(37)6-5-14(32)30(45)46/h2-4,14-16,35,41-42,47H,5-11,32H2,1H3,(H,33,44)(H,34,37)(H,38,39)(H,45,46)/t14-,15-,16-,31-/m0/s1 |
| Isomere SMILES | COC1=CC=CC2=C1C(=O)C3=C(C4=C(C[C@](C[C@@H]4O)(C(=O)CSC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N)O)C(=C3C2=O)O)O |
| PubChem CID | 70682637 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Klasse | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Peptides |
| Direct Parent | Oligopeptides |
| Alternative Parents | Gamma-glutamyl peptides Tetracenequinones Anthraquinones Glutamine and derivatives N-acyl-alpha amino acids Cysteine and derivatives Alpha amino acid amides Tetralins L-alpha-amino acids Anisoles Aryl ketones Alkyl aryl ethers Phenols Dicarboxylic acids and derivatives N-acyl amines Alpha-hydroxy ketones Tertiary alcohols Vinylogous acids Secondary carboxylic acid amides Secondary alcohols Amino acids Polyols Sulfenyl compounds Carboxylic acids Dialkylthioethers Monoalkylamines Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Alpha-oligopeptide - Gamma-glutamyl alpha peptide - Tetracenequinone - 1,4-anthraquinone - 9,10-anthraquinone - Glutamine or derivatives - Anthracene - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - Alpha-amino acid amide - Cysteine or derivatives - Alpha-amino acid - N-substituted-alpha-amino acid - L-alpha-amino acid - Alpha-amino acid or derivatives - Tetralin - Anisole - Phenol ether - Aryl ketone - Alkyl aryl ether - Phenol - N-acyl-amine - Dicarboxylic acid or derivatives - Fatty acyl - Benzenoid - Fatty amide - Vinylogous acid - Tertiary alcohol - Alpha-hydroxy ketone - Secondary alcohol - Secondary carboxylic acid amide - Amino acid - Ketone - Carboxamide group - Amino acid or derivatives - Thioether - Sulfenyl compound - Ether - Dialkylthioether - Carboxylic acid - Polyol - Alcohol - Carbonyl group - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Amine - Organosulfur compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Aromatic homopolycyclic compound |
| Beschreibung | 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 |
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
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