Midecamycin

CAT: 0013-GTR19158449-04Size: 25 mgDry Ice: NoHazardous: No

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CAT#:0013-GTR19158449-04Size:25 mg

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Description

Midecamycin an acetoxy-substituted macrolide antibiotic has effective on gram-positive and gram-negative bacteria acts by inhibiting bacterial protein synthesis. (In Vitro) :Midecamycin inhibits the majority of streptococci, staphylococci, and strains of Haemophilus and Listeria at concentrations of less than 3.1 μg/mL. Midecamycin is a 16-membered macrolide. Midecamycin is a new macrolide antibiotic, which is produced by Streptomyces mycarofaciens.

CAS Number

35457-80-8

Product Name Alternative

Purity

>98% (HPLC)

Solubility

DMSO: 50 mg/mL; Ethanol: 50 mg/mL; Water: Insoluble

Smiles

CCC (=O) O[C@H]1[C@H] (C) O[C@H] (C[C@@]1 (C) O) O[C@@H]1[C@@H] (C) O[C@@H] (O[C@H]2[C@@H] (CC=O) C[C@@H] (C) [C@@H] (O) \C=C\C=C\C[C@@H] (C) OC (=O) C[C@@H] (OC (=O) CC) [C@@H]2OC) [C@H] (O) [C@H]1N (C) C

Molecular Formula

C41H67NO15

Molecular Weight

813.97

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

7- (Formylmethyl) -410-dihydroxy-5-methoxy-916-dimethyl-2-oxooxacyclohexadeca-1113-dien-6-yl 36-dideoxy-4-O- (26-dideoxy-3-C-methyl-alpha-L-ribo-hexopyranosyl) -3- (dimethylamino) -beta-D-glucopyranoside 4'4''-dipropionate (ester)

Chemical Information

Midecamycin

Midecamycin is an organic molecular entity.

CAS Number	35457-80-8
PubChem CID	5282169
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
Molecular Formula	C41H67NO15
Molecular Weight	814.0
XLogP	2.6
Topological Polar Surface Area	206
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	16
Rotatable Bond Count	14
Heavy Atom Count	57
Formal Charge	0
Complexity	1360

SMILES

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

InChI

InChI=1S/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

InChIKey

DMUAPQTXSSNEDD-QALJCMCCSA-N

Chemical Structure

2D Structure

CAS: 35457-80-8

CID: 5282169

Formula: C41H67NO15

MW: 814.0

Interactive 3D Structure

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View on PubChem Raw 3D data

Computed Properties

Property	Value
Molecular Weight	814.0
XLogP3	2.6
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	16
Rotatable Bond Count	14
Exact Mass	813.45107043
Monoisotopic Mass	813.45107043
Topological Polar Surface Area	206 Å²
Heavy Atom Count	57
Formal Charge	0
Complexity	1360
Isotope Atom Count	0
Defined Atom Stereocenter Count	16
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	2
Undefined Bond Stereocenter Count	0
Covalently-Bonded Unit Count	1
Compound Is Canonicalized	Yes

Alternative Products

Catalog	Name
BA1041-500	Midecamycin
A17683-500	Midecamycin 500mg
A17683-100	Midecamycin 100mg
HY-N14865	Midecamycin A4

Midecamycin

Chemical Information

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