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Cardiolipin Biosynthesis CL(a-13:0/a-25:0/18:2(9Z,11Z)/a-13:0)[rac]
smpdb.ca/view/SMP0371326MetabolicLast, cardiolipin synthase catalyzes the synthesis of cardiolipin by transferring a phosphatidyl group from a second CDP-diacylglycerol to PG. It requires a divalent metal cation cofactor.
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-13:0/18:2(9Z,11Z))[rac]
smpdb.ca/view/SMP0371344MetabolicLast, cardiolipin synthase catalyzes the synthesis of cardiolipin by transferring a phosphatidyl group from a second CDP-diacylglycerol to PG. It requires a divalent metal cation cofactor.
Malignant Neoplasms
go.drugbank.com/conditions/DBCOND0029679Drugs: OxygenSynonyms: Malignant neoplasm without specification of site, [X]Malignant neoplasm without specification of site (disorder)Glutamyl aminopeptidase
go.drugbank.com/bio_entities/BE0002271TargetHumansRegulates central hypertension through its calcium-modulated preference to cleave N-terminal acidic residues from peptides such as angiotensin II
Synonyms: AP-A, Aminopeptidase ACrohn's Ileocolitis
go.drugbank.com/conditions/DBCOND0073538Drugs: MesalazineSynonyms: Crohn's disease, unspecified, without complicationsFever
go.drugbank.com/conditions/DBCOND0020923Drugs: Acetaminophen · Acetylsalicylic acid · Ascorbic acid · Brompheniramine · Caffeine · Chlorpheniramine +20 moreSynonyms: Has a temperatureUncharacterized MFS-type transporter EfpA
go.drugbank.com/bio_entities/BE0009715TargetMycobacterium tuberculosis (strain ATCC 25618 / H37Rv)Synonyms: Efflux protein AGastro-esophageal Reflux Disease (GERD)
go.drugbank.com/conditions/DBCOND0077290Drugs: Alginic acid · Aluminum hydroxide · Belladonna · Calcium carbonate · Cimetidine · Cinitapride +14 moreSynonyms: Gastro-esophageal reflux disease without esophagitis, Oesophageal reflux (& [without mention of oesophagitis])Febrile Illness Acute
go.drugbank.com/conditions/DBCOND0059951Drugs: AcetaminophenSynonyms: Has a temperatureVitamin A Deficiency
smpdb.ca/view/SMP0125788DiseaseVitamin A deficiency can be caused by many causes. A defect in the BCMO1 gene which codes for beta,beta-carotene 15,15’-monooxygenase is one of them. … A defect in this enzyme results in decrease of levels of retinal and vitamin A in serum; Signs and symptoms include night blindness, poor adaptation to darkness, dry skin and hair.