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WX-554
go.drugbank.com/drugs/DB21749InvestigationalWX-554 is under investigation in clinical trial NCT01581060 (Phase I/II Dose-escalation Study to Investigate Safety and Pharmacokinetics/ Pharmacodynamics of WX-554 in Patients With Solid Tumours).
Cardiolipin Biosynthesis CL(a-13:0/a-15:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0044062DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-17:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0044383DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-21:0/a-25:0)
smpdb.ca/view/SMP0045011DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-25:0/a-13:0)
smpdb.ca/view/SMP0045025DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-25:0/a-17:0)
smpdb.ca/view/SMP0045027DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-25:0/i-17:0)
smpdb.ca/view/SMP0045035DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-25:0/i-19:0)
smpdb.ca/view/SMP0045037DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-25:0/i-20:0)
smpdb.ca/view/SMP0045038DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-25:0/i-24:0)
smpdb.ca/view/SMP0045041DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).