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Erythromycin lactobionate - 615u/mg, high purity , Bacterial 70S ribosome inhibitor, CAS No.3847-29-8, Bacterial 70S ribosome inhibitor

COA

Grade & Purity:

615u/mg

Cas Number: 3847-29-8
Molecular Weight: 1092.22
PubChem CID: 71469

In stock

Item Number

E333646

Grouped product items
SKU	Size	Availability	Price	Qty
E333646-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$126.90

View related series

Anti-infection (2803) Antibiotic (1629) Bacterial (3013) Cell Cycle (2830)

Basic Description

Synonyms	DTXCID401436149 \| Erythromycin mono(4-O-beta-D-galactopyranosyl-D-gluconate) (salt) \| ERYTHROMYCINI LACTOBIONAS [WHO-IP LATIN] \| EINECS 223-348-7 \| ERYTHROMYCIN LACTOBIONATE (MART.) \| Q27256272 \| Metylohydrazyna \| RK363YG315 \| STERILE ERYTHROMYCIN LACTOBI
Specifications & Purity	615u/mg
Storage Temp	Store at 2-8°C,Desiccated
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Action Type	INHIBITOR
Mechanism of action	Bacterial 70S ribosome inhibitor

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbohydrates and carbohydrate conjugates
      - Level5 Aminosaccharides
        Level6 Aminoglycosides

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes	Aminosaccharides
Direct Parent	Aminoglycosides
Alternative Parents	Fatty acyl glycosides of mono- and disaccharides Macrolides and analogues Disaccharides O-glycosyl compounds Medium-chain hydroxy acids and derivatives Medium-chain fatty acids Sugar acids and derivatives Beta hydroxy acids and derivatives Heterocyclic fatty acids Hydroxy fatty acids Alpha hydroxy acids and derivatives Oxanes Tertiary alcohols 1,2-aminoalcohols Trialkylamines Amino acids and derivatives Secondary alcohols Carboxylic acid esters Cyclic ketones Lactones Dialkyl ethers Acetals Polyols Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Primary alcohols Hydrocarbon derivatives Organopnictogen compounds Organic oxides
Molecular Framework	Not available
Substituents	Aminoglycoside core - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Macrolide - Gluconic_acid - Glycosyl compound - O-glycosyl compound - Disaccharide - Medium-chain hydroxy acid - Medium-chain fatty acid - Heterocyclic fatty acid - Sugar acid - Hydroxy fatty acid - Beta-hydroxy acid - Fatty acyl - Fatty acid - Alpha-hydroxy acid - Hydroxy acid - Oxane - Tertiary alcohol - 1,2-aminoalcohol - Amino acid or derivatives - Carboxylic acid ester - Cyclic ketone - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Ketone - Lactone - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Ether - Polyol - Dialkyl ether - Carboxylic acid - Acetal - Carboxylic acid derivative - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Amine - Alcohol - Organopnictogen compound - Organic oxide - Primary alcohol - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
Description	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
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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	(3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione;(2R,3R,4R,5R)-2,3,5,6-tetrahydroxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanoic acid
INCHI	InChI=1S/C37H67NO13.C12H22O12/c1-14-25-37(10,45)30(41)20(4)27(39)18(2)16-35(8,44)32(51-34-28(40)24(38(11)12)15-19(3)47-34)21(5)29(22(6)33(43)49-25)50-26-17-36(9,46-13)31(42)23(7)48-26;13-1-3(15)10(7(18)8(19)11(21)22)24-12-9(20)6(17)5(16)4(2-14)23-12/h18-26,28-32,34,40-42,44-45H,14-17H2,1-13H3;3-10,12-20H,1-2H2,(H,21,22)/t18-,19-,20+,21+,22-,23+,24+,25-,26+,28-,29+,30-,31+,32-,34+,35-,36-,37-;3-,4-,5+,6+,7-,8-,9-,10-,12+/m11/s1
InChIKey	NNRXCKZMQLFUPL-WBMZRJHASA-N
Smiles	CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O.C(C1C(C(C(C(O1)OC(C(CO)O)C(C(C(=O)O)O)O)O)O)O)O
Isomeric SMILES	CC[C@@H]1[C@@]([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]2C[C@@]([C@H]([C@@H](O2)C)O)(C)OC)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)O)C)C)O)(C)O.C([C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)O[C@H]([C@@H](CO)O)[C@@H]([C@H](C(=O)O)O)O)O)O)O)O
Molecular Weight	1092.22
Reaxy-Rn	25684678
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25684678&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Solubility	Soluble in water, methanol, and alcohol.
Melt Point(°C)	>166° C (dec.)
Molecular Weight	1092.200 g/mol
XLogP3
Hydrogen Bond Donor Count	14
Hydrogen Bond Acceptor Count	26
Rotatable Bond Count	15
Exact Mass	1091.57 Da
Monoisotopic Mass	1091.57 Da
Topological Polar Surface Area	412.000 Å²
Heavy Atom Count	75
Formal Charge	0
Complexity	1580.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	27
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	2

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