Framycetin Impurity 5 (Framycetin EP Impurity E)

cas: 7542-37-2 — see every product listed under this CAS number, including other names

Framycetin Impurity 5 (Framycetin EP Impurity E) (CAS 7542-37-2) is a chemical reagent available from Chemat. Available pack sizes: 10mg, 25mg, 50mg, 100mg, 200mg. Offered by: Hubei YoungXin.

brandHubei YoungXin
catalog number27205F-10mg
cas7542-37-2
size10mg
availability Do potwierdzenia przez Chemat|To be confirmed by Chemat
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Available pack sizes

brand size price
Hubei YoungXin 10mg price on request
Hubei YoungXin 25mg price on request
Hubei YoungXin 50mg price on request
Hubei YoungXin 100mg price on request
Hubei YoungXin 200mg price on request

properties

purityNo data
delivery timeTo be confirmed by Chemat

Paromomycin is an amino cyclitol glycoside that is the 1-O-(2-amino-2-deoxy-alpha-D-glucopyranoside) and the 3-O-(2,6-diamino-2,6-dideoxy-beta-L-idopyranosyl)-beta-D-ribofuranoside of 4,6-diamino-2,3-dihydroxycyclohexane (the 1R,2R,3S,4R,6S diastereoisomer). It is obtained from various Streptomyces species. A broad-spectrum antibiotic, it is used (generally as the sulfate salt) for the treatment of acute and chronic intestinal protozoal infections, but is not effective for extraintestinal protozoal infections. It is also used as a therapeutic against visceral leishmaniasis. It has a role as an antiparasitic agent, an anthelminthic drug, an antiprotozoal drug and an antibacterial drug. It is an amino cyclitol glycoside and an aminoglycoside antibiotic. It is functionally related to a streptamine. It is a conjugate base of a paromomycin(5+).

Source: ChEBI

Identity
Molecular formulaC23H45N5O14
Molecular weight615.6 g/mol
IUPAC name(2S,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-[(2R,3S,4R,5S)-5-[(1R,2R,3S,5R,6S)-3,5-diamino-2-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxycyclohexyl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxyoxane-3,4-diol
InChIKeyUOZODPSAJZTQNH-LSWIJEOBSA-N
SMILESC1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)N)O[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O[C@@H]4[C@@H]([C@H]([C@@H]([C@@H](O4)CN)O)O)N)O)O)N

Computed by PubChem (NCBI)

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