Exact Mass: 472.1124116
Exact Mass Matches: 472.1124116
Found 27 metabolites which its exact mass value is equals to given mass value 472.1124116
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Clofazimine
A fat-soluble riminophenazine dye used for the treatment of leprosy. It has been used investigationally in combination with other antimycobacterial drugs to treat Mycobacterium avium infections in AIDS patients. Clofazimine also has a marked anti-inflammatory effect and is given to control the leprosy reaction, erythema nodosum leprosum. (From AMA Drug Evaluations Annual, 1993, p1619) J - Antiinfectives for systemic use > J04 - Antimycobacterials > J04B - Drugs for treatment of lepra > J04BA - Drugs for treatment of lepra D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007917 - Leprostatic Agents COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C254 - Anti-Infective Agent > C258 - Antibiotic D000893 - Anti-Inflammatory Agents Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
Compound WIN VIII
Aesculetin-6-O-beta-D-apiofuranosyl-(1->6)-O-beta-glucopyranoside
5,7-dihydroxycoumarin 7-(6-O-beta-D-apiofuranosyl-beta-D-glucopyranoside)|5,7-dihydroxycoumarin 7-O-beta-D-apiofuranosyl-(1->6)-O-beta-D-glucopyranoside|7-[(6-O-D-apio-beta-D-furanosyl-beta-D-glucopyranosyl)oxy]-5-hydroxy-2H-1-benzopyran-2-one
clofazimine
J - Antiinfectives for systemic use > J04 - Antimycobacterials > J04B - Drugs for treatment of lepra > J04BA - Drugs for treatment of lepra D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007917 - Leprostatic Agents COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C254 - Anti-Infective Agent > C258 - Antibiotic D000893 - Anti-Inflammatory Agents Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
L-732,138
L-732138 is a selective, potent and competitive neurokinin-1 (NK-1) receptor antagonist with an IC50 of 2.3 nM. L-732138 has 200-fold more potent in cloned human NK-1 receptors than cloned rat NK-1 receptors, and has > 1000-fold more potent than human NK-2 and NK-3 receptors. L-732138 can reduce hyperalgesia and has antitumor action[1][2].
SODIUM PHENYLBENZIMIDAZOLE SULFONATE
C23H22Cl2N4O3 (472.10688819999996)
sodium 1-amino-4-[(4-butylphenyl)amino]-9,10-dihydro-9,10-dioxoanthracene-2-sulphonate
C24H21N2NaO5S (472.10688160000007)
1-(3,5-Di-O-benzoyl-2-deoxy-2-fluoro-beta-L-arabinofuranosyl)-5-fluoro-2,4(1H,3H)-pyrimidinedione
C23H18F2N2O7 (472.10820219999994)
3-Benzyl-3,6-bis(cysteinyl)-6-(hydroxymethyl)-diketopiperazine
C18H24N4O7S2 (472.10863539999997)
(2R)-2-amino-3-[(2R,5R)-5-[(2R)-2-amino-2-carboxyethyl]sulfanyl-2-benzyl-5-(hydroxymethyl)-3,6-dioxopiperazin-2-yl]sulfanylpropanoic acid
C18H24N4O7S2 (472.10863539999997)