Dirithromycin - ≥97% , CAS No.62013-04-1

CAS: 62013-04-1 Cat. No.: D129588 Summenformel: C₄₂H₇₈N₂O₁₄ Molekulargewicht: 835.07 EG-Nummer: 624-080-7

GRADE & PURITY ≥97%

Synonyms

LY-237216 | cid_6473883 | DIRITHROMYCIN [USAN] | BSPBio_000633 | KBioSS_001956 | 2-flurobenzaldehyde | AMY36997 | Dynabac | Prestwick3_000557 | BDBM59397 | (1S,2R,3R,6R,7S,8S,9R,10R,12R,13S,15R,17S)-9-[(2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyloxa

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Dirithromycin is a macrolide glycopeptide antibiotic by binding to the 50S subunit of the 70S bacterial ribosome to inhibit the translocation of peptides.
A semi-synthetic derivative of Erythromycin that acts as an antibacterial.

Specifications

Synonyme

LY-237216 | cid_6473883 | DIRITHROMYCIN [USAN] | BSPBio_000633 | KBioSS_001956 | 2-flurobenzaldehyde | AMY36997 | Dynabac | Prestwick3_000557 | BDBM59397 | (1S,2R,3R,6R,7S,8S,9R,10R,12R,13S,15R,17S)-9-[(2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyloxa

Spezifikationen & Reinheit

≥97%

Biochemische und physiologische Mechanismen

Dirithromycin is a semi-synthetic derivative of Erythromycin, and an antibacterial.

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

INHIBITOR

Reinheit

≥97%

Namen und Kennungen

Pubchem Sid

504764244

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504764244

Kanonisches Lächeln

CCC1C(C2C(C(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)NC(O2)COCCOC)C)(C)O

IUPAC Name

(1R,2R,3R,6R,7S,8S,9R,10R,12R,13S,15R,17S)-9-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-3-ethyl-2,10-dihydroxy-7-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-15-(2-methoxyethoxymethyl)-2,6,8,10,12,17-hexamethyl-4,16-dioxa-14-azabicyclo[11.3.1]heptadecan-5-one

InChIKey

WLOHNSSYAXHWNR-DWIOZXRMSA-N

INCHI

1S/C42H78N2O14/c1-15-29-42(10,49)37-24(4)32(43-30(56-37)21-52-17-16-50-13)22(2)19-40(8,48)36(58-39-33(45)28(44(11)12)18-23(3)53-39)25(5)34(26(6)38(47)55-29)57-31-20-41(9,51-14)35(46)27(7)54-31/h22-37,39,43,45-46,48-49H,15-21H2,1-14H3/t22-,23-,24+,25+,26-,27+,28+,29-,30-,31+,32+,33-,34+,35+,36-,37-,39+,40-,41-,42-/m1/s1

Isomere SMILES

CC[C@@H]1[C@@]([C@H]2[C@H]([C@H]([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)N[C@H](O2)COCCOC)C)(C)O

WGK Deutschland

3

Molekulargewicht

835.07

Reaxy-Rn

604832

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=604832&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Ebene5 Aminosaccharides
          • Ebene6 Aminoglycosides

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Aminosaccharides
• Direct Parent: Aminoglycosides
• Alternative Parents: Macrolides and analogues O-glycosyl compounds Oxanes 1,3-oxazinanes Monosaccharides Tertiary alcohols Trialkylamines Secondary alcohols Amino acids and derivatives 1,2-aminoalcohols Carboxylic acid esters Lactones Hemiaminals Acetals Dialkylamines Dialkyl ethers Monocarboxylic acids and derivatives Oxacyclic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Aminoglycoside core - Macrolide - O-glycosyl compound - Glycosyl compound - Monosaccharide - 1,3-oxazinane - Oxane - Oxazinane - Tertiary alcohol - Tertiary amine - Lactone - Secondary alcohol - Tertiary aliphatic amine - Hemiaminal - Carboxylic acid ester - Amino acid or derivatives - 1,2-aminoalcohol - Acetal - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Secondary aliphatic amine - Ether - Azacycle - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Organic nitrogen compound - Alcohol - Amine - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Organopnictogen compound - Aliphatic heteropolycyclic compound
• Beschreibung: 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: macrolide antibiotic

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.

DOI: 10.1186/s13321-016-0174-y

Chemische und physikalische Eigenschaften

• Löslichkeit: DMSO 11 mg/mL Water <1 mg/mL Ethanol 100 mg/mL
• Empfindlichkeit: Heat Sensitive
• Spezifische Drehung [α]: -88° (C=1,MeOH)
• Schmelzpunkt (°C): 188 °C
• Molekulargewicht: 835.100 g/mol
• XLogP3: 4.200
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 16
• Rotatable Bond Count: 12
• Exact Mass: 834.545 Da
• Monoisotopic Mass: 834.545 Da
• Topological Polar Surface Area: 196.000 Ų
• Heavy Atom Count: 58
• Formal Charge: 0
• Complexity: 1300.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 20
• 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