≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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.
Davercin is a first generation semi-synthetic erythromycin. Davercin is prepared by coupling the 11- and 12-OH groups to form a cyclic carbonate. This simple modification improves the stability and hydrophobicity of the macrocyclic structure. Davercin shows comparable or better in vitro potency, low host toxicity and improved pharmacokinetics compared with erythromycin.
| Pubchem Sid | 488196501 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488196501 |
| Sonrisas canónicas | CCC1C2(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC3CC(C(C(O3)C)O)(C)OC)C)OC4C(C(CC(O4)C)N(C)C)O)(C)O)C)C)OC(=O)O2)C |
| IUPAC Name | (1R,2R,5R,6S,7S,8R,9R,11R,13R,14R)-8-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-9-hydroxy-6-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-1,5,7,9,11,13-hexamethyl-3,15,17-trioxabicyclo[12.3.0]heptadecane-4,12,16-trione |
| InChIKey | NKLGIWNNVDPGCA-ZDYKNUMJSA-N |
| INCHI | 1S/C38H65NO14/c1-14-25-38(10)32(52-35(44)53-38)20(4)27(40)18(2)16-36(8,45)31(51-34-28(41)24(39(11)12)15-19(3)47-34)21(5)29(22(6)33(43)49-25)50-26-17-37(9,46-13)30(42)23(7)48-26/h18-26,28-32,34,41-42,45H,14-17H2,1-13H3/t18-,19-,20+,21+,22-,23+,24+,25-,26+,28-,29+,30+,31-,32-,34+,36-,37-,38-/m1/s1 |
| Isómeros SMILES | CC[C@@H]1[C@@]2([C@@H]([C@H](C(=O)[C@@H](C[C@@]([C@@H]([C@H]([C@@H]([C@H](C(=O)O1)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)O)(C)OC)C)O[C@H]4[C@@H]([C@H](C[C@H](O4)C)N(C)C)O)(C)O)C)C)OC(=O)O2)C |
| RTECS | KF46700000 |
| PubChem CID | 10033072 |
| Peso molecular | 759.92 |
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 oxygen compounds |
| Clase | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Aminosaccharides |
| Direct Parent | Aminoglycosides |
| Alternative Parents | Macrolides and analogues O-glycosyl compounds Carbonic acid diesters Monosaccharides Oxanes Tertiary alcohols 1,3-dioxolanes Secondary alcohols Amino acids and derivatives 1,2-aminoalcohols Trialkylamines Lactones Carboxylic acid esters Cyclic ketones Acetals Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Organopnictogen compounds Hydrocarbon derivatives Aldehydes |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | Aminoglycoside core - Macrolide - Glycosyl compound - O-glycosyl compound - Carbonic acid diester - Monosaccharide - Oxane - Tertiary alcohol - Meta-dioxolane - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Cyclic ketone - Amino acid or derivatives - Carbonic acid derivative - 1,2-aminoalcohol - Carboxylic acid ester - Ketone - Lactone - Oxacycle - Organoheterocyclic compound - Acetal - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Dialkyl ether - Ether - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aldehyde - Amine - Organopnictogen compound - Organic oxide - Aliphatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 C2618142 | Certificate of Analysis | Mar 30, 2026 | D333728 |
| C2329921 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2329925 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330018 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330027 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330029 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330050 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330090 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330224 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330630 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| C2330656 | Certificate of Analysis | Jan 19, 2026 | D333728 |
| L2409188 | Certificate of Analysis | Feb 13, 2023 | D333728 |
| Solubilidad | Soluble in ethanol, methanol, DMF, DMSO. Limited water solubility. |
|---|---|
| Índice de refracción | n20D1.53 (Predicted) |
| Punto de ebullición (°C) | 859.75 °C at 760 mmHg (Predicted) |
| Peso molecular | 759.900 g/mol |
| XLogP3 | 4.100 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 15 |
| Rotatable Bond Count | 7 |
| Exact Mass | 759.441 Da |
| Monoisotopic Mass | 759.441 Da |
| Topological Polar Surface Area | 189.000 Ų |
| Heavy Atom Count | 53 |
| Formal Charge | 0 |
| Complexity | 1300.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 18 |
| 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 |
