Salinosporamide A (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Salinosporamide A" in English language version.

refsWebsite

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10nih.gov

4^th place

9doi.org

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1cancer.gov

1,684^th place

1,350^th place

1semanticscholar.org

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8^th place

1myelomabeacon.com

low place

1clinicaltrials.gov

5,225^th place

4,062^nd place

cancer.gov

dtp.cancer.gov

"MDA-MB-435, and its derivation MDA-N, are Melanoma cell lines, not breast cancer cell lines". Developmental Therapeutics Program. National Cancer Institute. 8 May 2015. Retrieved 6 January 2018.

clinicaltrials.gov

ClinicalTrials.gov: Marizomib

doi.org

Feling RH; Buchanan GO; Mincer TJ; Kauffman CA; Jensen PR; Fenical W (2003). "Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora". Angew. Chem. Int. Ed. Engl. 42 (3): 355–7. doi:10.1002/anie.200390115. PMID 12548698.
Chauhan D, Catley L, Li G, et al. (2005). "A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib". Cancer Cell. 8 (5): 407–19. doi:10.1016/j.ccr.2005.10.013. PMID 16286248.
Beer LL; Moore BS (2007). "Biosynthetic convergence of salinosporamides A and B in the marine actinomycete Salinispora tropica". Org. Lett. 9 (5): 845–8. doi:10.1021/ol063102o. PMID 17274624.
Vaillancourt FH; Yeh E; Vosburg DA; Garneau-Tsodikova S; Walsh CT (2006). "Nature's inventory of halogenation catalysts: oxidative strategies predominate". Chem. Rev. 106 (8): 3364–78. doi:10.1021/cr050313i. PMID 16895332.
Tsueng G; McArthur KA; Potts BC; Lam KS (2007). "Unique butyric acid incorporation patterns for salinosporamides A and B reveal distinct biosynthetic origins". Applied Microbiology and Biotechnology. 75 (5): 999–1005. doi:10.1007/s00253-007-0899-7. PMID 17340108. S2CID 8992755.
Reddy LR; Saravanan P; Corey EJ (2004). "A simple stereocontrolled synthesis of salinosporamide A". J. Am. Chem. Soc. 126 (20): 6230–1. doi:10.1021/ja048613p. PMID 15149210.
Ling T; Macherla VR; Manam RR; McArthur KA; Potts BC (2007). "Enantioselective Total Synthesis of (−)-Salinosporamide A (NPI-0052)". Org. Lett. 9 (12): 2289–92. doi:10.1021/ol0706051. PMID 17497868.
Ma G; Nguyen H; Romo D (2007). "Concise Total Synthesis of (±)-Salinosporamide A, (±)-Cinnabaramide A, and Derivatives via a Bis-Cyclization Process: Implications for a Biosynthetic Pathway?". Org. Lett. 9 (11): 2143–6. doi:10.1021/ol070616u. PMC 2518687. PMID 17477539.
Endo A; Danishefsky SJ (2005). "Total synthesis of salinosporamide A". J. Am. Chem. Soc. 127 (23): 8298–9. doi:10.1021/ja0522783. PMID 15941259.

myelomabeacon.com

"Marizomib May Be Effective In Relapsed/Refractory Multiple Myeloma (ASH 2011)". The Myeloma Beacon. 2012-01-23. Retrieved 2012-06-10.

nih.gov

pubmed.ncbi.nlm.nih.gov

Feling RH; Buchanan GO; Mincer TJ; Kauffman CA; Jensen PR; Fenical W (2003). "Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora". Angew. Chem. Int. Ed. Engl. 42 (3): 355–7. doi:10.1002/anie.200390115. PMID 12548698.
Chauhan D, Catley L, Li G, et al. (2005). "A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib". Cancer Cell. 8 (5): 407–19. doi:10.1016/j.ccr.2005.10.013. PMID 16286248.
Beer LL; Moore BS (2007). "Biosynthetic convergence of salinosporamides A and B in the marine actinomycete Salinispora tropica". Org. Lett. 9 (5): 845–8. doi:10.1021/ol063102o. PMID 17274624.
Vaillancourt FH; Yeh E; Vosburg DA; Garneau-Tsodikova S; Walsh CT (2006). "Nature's inventory of halogenation catalysts: oxidative strategies predominate". Chem. Rev. 106 (8): 3364–78. doi:10.1021/cr050313i. PMID 16895332.
Tsueng G; McArthur KA; Potts BC; Lam KS (2007). "Unique butyric acid incorporation patterns for salinosporamides A and B reveal distinct biosynthetic origins". Applied Microbiology and Biotechnology. 75 (5): 999–1005. doi:10.1007/s00253-007-0899-7. PMID 17340108. S2CID 8992755.
Reddy LR; Saravanan P; Corey EJ (2004). "A simple stereocontrolled synthesis of salinosporamide A". J. Am. Chem. Soc. 126 (20): 6230–1. doi:10.1021/ja048613p. PMID 15149210.
Ling T; Macherla VR; Manam RR; McArthur KA; Potts BC (2007). "Enantioselective Total Synthesis of (−)-Salinosporamide A (NPI-0052)". Org. Lett. 9 (12): 2289–92. doi:10.1021/ol0706051. PMID 17497868.
Ma G; Nguyen H; Romo D (2007). "Concise Total Synthesis of (±)-Salinosporamide A, (±)-Cinnabaramide A, and Derivatives via a Bis-Cyclization Process: Implications for a Biosynthetic Pathway?". Org. Lett. 9 (11): 2143–6. doi:10.1021/ol070616u. PMC 2518687. PMID 17477539.
Endo A; Danishefsky SJ (2005). "Total synthesis of salinosporamide A". J. Am. Chem. Soc. 127 (23): 8298–9. doi:10.1021/ja0522783. PMID 15941259.

ncbi.nlm.nih.gov

Ma G; Nguyen H; Romo D (2007). "Concise Total Synthesis of (±)-Salinosporamide A, (±)-Cinnabaramide A, and Derivatives via a Bis-Cyclization Process: Implications for a Biosynthetic Pathway?". Org. Lett. 9 (11): 2143–6. doi:10.1021/ol070616u. PMC 2518687. PMID 17477539.

semanticscholar.org

api.semanticscholar.org

Tsueng G; McArthur KA; Potts BC; Lam KS (2007). "Unique butyric acid incorporation patterns for salinosporamides A and B reveal distinct biosynthetic origins". Applied Microbiology and Biotechnology. 75 (5): 999–1005. doi:10.1007/s00253-007-0899-7. PMID 17340108. S2CID 8992755.