Exact Mass: 432.2067

Exact Mass Matches: 432.2067

Found 6 metabolites which its exact mass value is equals to given mass value 432.2067, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

Mizolastine

2-[(1-{1-[(4-fluorophenyl)methyl]-1H-1,3-benzodiazol-2-yl}piperidin-4-yl)(methyl)amino]pyrimidin-4-ol

C24H25FN6O (432.2074)


R - Respiratory system > R06 - Antihistamines for systemic use > R06A - Antihistamines for systemic use D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists Mizolastine (mizollen) is a second-generation piperidine H1-antihistamine. C308 - Immunotherapeutic Agent > C29578 - Histamine-1 Receptor Antagonist Mizolastine is an orally active, high affinity and specific peripheral histamine H1 receptor antagonist (second generation antihistamine). Mizolastine effectively inhibits mRNA expression of VEGF165, VEGF120, TNF-α and KC. Mizolastine can be used in studies of allergic rhinitis and chronic idiopathic urticarial[1][2][3].

   

Mizolastine (Mizollen)

Mizolastine (Mizollen)

C24H25FN6O (432.2074)


   

Miransertib

Miransertib

C27H24N6 (432.2062)


C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C61074 - Serine/Threonine Kinase Inhibitor C274 - Antineoplastic Agent > C1742 - Angiogenesis Inhibitor > C155764 - AKT Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor Miransertib (ARQ-092) is a potent, orally active, selective and allosteric Akt inhibitor with IC50s of 2.7 nM, 14 nM and 8.1 nM for Akt1, Akt2, Akt3, respectively. Miransertib is also a potent the AKT1-E17K mutant protein inhibitor and has the potential for PI3K/AKT-driven tumors and Proteus syndrome research[1]. Miransertib is effective against Leishmania[2].

   

Mizolastine

Mizolastine

C24H25FN6O (432.2074)


R - Respiratory system > R06 - Antihistamines for systemic use > R06A - Antihistamines for systemic use D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists C308 - Immunotherapeutic Agent > C29578 - Histamine-1 Receptor Antagonist Mizolastine is an orally active, high affinity and specific peripheral histamine H1 receptor antagonist (second generation antihistamine). Mizolastine effectively inhibits mRNA expression of VEGF165, VEGF120, TNF-α and KC. Mizolastine can be used in studies of allergic rhinitis and chronic idiopathic urticarial[1][2][3].

   

(4s,7s,12r,12as,14as,18r,18ar,18br)-2-chloro-1-hydroxy-4,7,12,18-tetramethyl-4h,7h,12h,12ah,14ah,15h,16h,17h,18h,18ah,18bh-naphtho[1,2-g]oxacyclotetradecane-3,5-dione

(4s,7s,12r,12as,14as,18r,18ar,18br)-2-chloro-1-hydroxy-4,7,12,18-tetramethyl-4h,7h,12h,12ah,14ah,15h,16h,17h,18h,18ah,18bh-naphtho[1,2-g]oxacyclotetradecane-3,5-dione

C25H33ClO4 (432.2067)


   

9-methylacridine-3,6-diamine; proflavine

9-methylacridine-3,6-diamine; proflavine

C27H24N6 (432.2062)