Midecamycin - 10mM in DMSO , CAS No.35457-80-8

CAS: 35457-80-8 Cat. No.: M423587 Fórmula: C41H67NO15 Peso molecular: 814 Número CE: 252-578-0 PubChem CID: 5282169
Disponível para encomenda
GRADE & PURITY 10mM in DMSO
Synonyms
EINECS 252-578-0 | YL 704 B1 | MIDECAMYCIN [JAN] | Tox21_110635 | Midecamicina [INN-Spanish] | Antibiotic YL 704 B1 | D01339 | Midecamycine [INN-French] | NCGC00016830-01 | Espinomycin A | sf-837 | Turimycin P(sub 3) | DB13456 | Medecamycin A1 | N34Z0Y5UH
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
Size
Alemanha (EU)
USA*
Price
Qty
1ml
M423587-1ml
1 Em stock

41,56€

60,65€
Gravar 19,09 € (31.47%)
Enter a quantity for the sizes you want to add.
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

Midecamycin, an acetoxy-substituted macrolide antibiotic, is tested against gram-positive and gram-negative bacteria.

Specifications

Sinónimos
EINECS 252-578-0 | YL 704 B1 | MIDECAMYCIN [JAN] | Tox21_110635 | Midecamicina [INN-Spanish] | Antibiotic YL 704 B1 | D01339 | Midecamycine [INN-French] | NCGC00016830-01 | Espinomycin A | sf-837 | Turimycin P(sub 3) | DB13456 | Medecamycin A1 | N34Z0Y5UH
Especificações e pureza
10mM in DMSO
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Propriedades do produto
pKapKₐ: 6.9 in 50% aq ethanol
Nomes e identificadores
Pubchem Sid528776682
Sorrisos canónicosCCC(=O)OC1CC(=O)OC(CC=CC=CC(C(CC(C(C1OC)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)OC(=O)CC)(C)O)N(C)C)O)CC=O)C)O)C
IUPAC Name[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-[(2S,3R,4R,5S,6R)-4-(dimethylamino)-3-hydroxy-5-[(2S,4R,5S,6S)-4-hydroxy-4,6-dimethyl-5-propanoyloxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-4-yl] propanoate
InChIKeyDMUAPQTXSSNEDD-QALJCMCCSA-N
INCHI1S/C41H67NO15/c1-11-30(45)54-29-21-32(47)51-24(4)16-14-13-15-17-28(44)23(3)20-27(18-19-43)37(38(29)50-10)57-40-35(48)34(42(8)9)36(25(5)53-40)56-33-22-41(7,49)39(26(6)52-33)55-31(46)12-2/h13-15,17,19,23-29,33-40,44,48-49H,11-12,16,18,20-22H2,1-10H3/b14-13+,17-15+/t23-,24-,25-,26+,27+,28+,29-,33+,34-,35-,36-,37+,38+,39+,40+,41-/m1/s1
SMILES isoméricas CCC(=O)O[C@@H]1CC(=O)O[C@@H](C/C=C/C=C/[C@@H]([C@@H](C[C@@H]([C@@H]([C@H]1OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)OC(=O)CC)(C)O)N(C)C)O)CC=O)C)O)C
RTECS OH4730600
PubChem CID 5282169
Peso molecular 814

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides
Direct ParentAminoglycosides
Alternative Parents Macrolides and analogues  Disaccharides  O-glycosyl compounds  Tricarboxylic acids and derivatives  Oxanes  Alpha-hydrogen aldehydes  Tertiary alcohols  1,2-aminoalcohols  Trialkylamines  Amino acids and derivatives  Carboxylic acid esters  Secondary alcohols  Lactones  Acetals  Dialkyl ethers  Oxacyclic compounds  Hydrocarbon derivatives  Organopnictogen compounds  Organic oxides  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Aminoglycoside core - Macrolide - Disaccharide - Glycosyl compound - O-glycosyl compound - Tricarboxylic acid or derivatives - Oxane - Alpha-hydrogen aldehyde - Tertiary alcohol - 1,2-aminoalcohol - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary aliphatic amine - Secondary alcohol - Tertiary amine - Ether - Dialkyl ether - Carboxylic acid derivative - Acetal - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Alcohol - Carbonyl group - Organopnictogen compound - Aldehyde - Organonitrogen compound - Organic nitrogen compound - Amine - Aliphatic heteromonocyclic compound
DescriçãoThis 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
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
ABCC2 Tchem Canalicular multispecific organic anion transporter 1 (1191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCB11 Tchem Bile salt export pump (2311 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC3 Tbio Canalicular multispecific organic anion transporter 2 (718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC4 Tchem Multidrug resistance-associated protein 4 (785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
Índice de refraçãon20D1.54
Rotação específica [α]α23/D -67°, c = 1 in ethanol
Ponto de inflamação (°F)>110°(230°F)
Ponto de ebulição (°C)874° C
Ponto de fusão (°C)155-156° C
Peso molecular814.000 g/mol
XLogP32.600
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count16
Rotatable Bond Count14
Exact Mass813.451 Da
Monoisotopic Mass813.451 Da
Topological Polar Surface Area206.000 Ų
Heavy Atom Count57
Formal Charge0
Complexity1360.000
Isotope Atom Count0
Defined Atom Stereocenter Count16
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count2
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds2
Covalently-Bonded Unit Count1
Citations of This Product
Referências
1. Hongchao Dai, Lei Yuan, Luyao Fan, Jia Yang, Xinan Jiao.  (2024)  Occurrence and risk-related features of Bacillus cereus in fluid milk.  INTERNATIONAL JOURNAL OF DAIRY TECHNOLOGY,      [PMID:] [10.1111/1471-0307.13054]
2. Chu Fengjian, Zhao Gaosheng, Wei Wei, Shuaibu Nazifi Sani, Feng Hongru, Pan Yuanjiang, Wang Xiaozhi.  (2024)  Wide-energy programmable microwave plasma-ionization for high-coverage mass spectrometry analysis.  Nature Communications,  15  (1): (1-10).  [PMID:39025871] [10.1038/s41467-024-50322-z]
Calculadoras de soluções
Revisões

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