CAS 41411-66-9
:2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, [4S-(4α,4aα,5α,5aα,6β,12aα)]-
Description:
2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, with the CAS number 41411-66-9, is a complex organic compound characterized by its intricate molecular structure, which includes multiple hydroxyl groups and a naphthalene-derived framework. This compound features a dimethylamino group, contributing to its potential biological activity. The presence of multiple hydroxy groups suggests it may exhibit significant solubility in polar solvents and could participate in hydrogen bonding interactions. The hydrochloride form indicates that it is a salt, which can enhance its stability and solubility in aqueous environments. Such compounds are often investigated for their pharmacological properties, including potential antitumor or antimicrobial activities. The stereochemistry, indicated by the specific configuration descriptors, may also play a crucial role in determining the compound's biological interactions and efficacy. Overall, this substance represents a class of compounds that may have valuable applications in medicinal chemistry and drug development.
Formula:C22H25ClN2O8
InChI:InChI=1/C22H24N2O8.ClH/c1-7-8-5-4-6-9(25)11(8)16(26)12-10(7)17(27)14-15(24(2)3)18(28)13(21(23)31)20(30)22(14,32)19(12)29;/h4-7,10,14-15,17,25-27,31-32H,23H2,1-3H3;1H/b21-13-;
InChI key:InChIKey=RUYHIJHUVHIMIR-IBVFHKCESA-N
SMILES:O[C@]12[C@]([C@H](N(C)C)C(O)=C(C(N)=O)C1=O)([C@@H](O)[C@]3(C(=C2O)C(=O)C=4C([C@H]3C)=CC=CC4O)[H])[H].Cl
Synonyms:- (2Z)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methyl-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione hydrochloride
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, 6-epimer, monohydrochloride
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, (4S-(4alpha,4aalpha,5alpha,5aalpha,6beta,12aalpha))-
- 6-Epidoxycycline hydrochloride
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, [4S-(4α,4aα,5α,5aα,6β,12aα)]-
- 6-EPIDOXYCYCLINE HYDROCHLORIDE USP/EP/BP
- 6-Epidoxycycline hydrochl
- 6-epidoxycline hydrochloride
- 6-epidoxycyline hydrochloride
- Doxycyline Related Compound-A
- 6-Epidoxycycline HCl/Doxycycline EP Impurity A HCl
- (4S,4aR,5S,5aR,6S,12aS)-4-(Dimethylamino)-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride
- Doxycycline Related Compound A (10 mg) ((4S,4aR,5S,5aR,6S,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide, monohydrochloride)
- Doxycycline EP Impurity A HCl
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, 4S-(4.alpha.,4a.alpha.,5.alpha.,5a.alpha.,6.beta.,12a.alpha.)-
- DOXYCYCLINE 6-EPIMER HCL
- See more synonyms
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Found 4 products.
Doxycycline Related Compound A ((4S,4aR,5S,5aR,6S,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide, monohydrochloride)
CAS:Tetracyclines and their derivatives; salts thereofFormula:C22H24N2O8·HClColor and Shape:Light Yellow PowderMolecular weight:480.9 g/molPharmaVetResiMix 5 Tetracyclines-v10 10 µg/mL in Methanol
CAS:Controlled ProductColor and Shape:Colourless6-Epidoxycycline hydrochloride
CAS:<p>6-Epidoxycycline hydrochloride is a synthetic antibiotic that is prepared by the condensation of divinylbenzene and 6-aminopenicillanic acid. It has been found to have good antibacterial activity against Gram-positive bacteria. 6-Epidoxycycline hydrochloride has also been shown to be active against Gram-negative bacteria, but not as potent as other antibiotics in this class. The compound has been found to be stable in plasma and urine samples, but can react with acetonitrile. This reaction can lead to impurities that interfere with the analysis of the sample by chromatography. The compound has not been well studied for its side effects or toxicology, but it is thought to have similar effects to other members of this class of antibiotics.</p>Formula:C22H24N2O8·HClPurity:Min. 90 Area-%Color and Shape:White PowderMolecular weight:480.9 g/mol




