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Fumagillol Fumagillol is an analog of Fumagillin (F862650), a compound isolated from the fungus Aspergillus fumigatus. Fumagillin is an antimicrobial agent used in the treatment of microsporidiosis. Fumagillin shows promise as both an an anti-infective and antiangiogenic agent. Group: Biochemicals. Alternative Names: (3R,4S,5S,6R)-5-Methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]octan-6-ol; (3R,4S,5S,6R)-5-Methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-1-oxaspiro[2.5]octan-6-ol; [3R-[3α, 4α(2R*, 3R*), 5 β,6 β]]-5-Methoxy-4-[2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-1-oxaspiro[2.5]octan-6-ol; (-)-Fumagillol; FOS 37. Grades: Highly Purified. CAS No. 108102-51-8. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C??H??O?, Molecular Weight: 282.38. US Biological Life Sciences. USBiological 3
Worldwide
Fumagillol Fumagillol is a precursor of Fumagillin, which is an antimicrobial agent used for the treatment of microsporidiosis. Fumagillol also exhibits anti-infective and antiangiogenic effects. Synonyms: 1-Oxaspiro[2.5]octan-6-ol, 5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-, (3R,4S,5S,6R)-; (3R,4S,5S,6R)-5-Methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]octan-6-ol; 1-Oxaspiro[2.5]octan-6-ol, 5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-, (3R,4S,5S,6R)-; 1-Oxaspiro[2.5]octan-6-ol, 5-methoxy-4-[2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-, [3R-[3α,4α(2R*,3R*),5β,6β]]-; (-)-Fumagillol; FOS 37; Gelcohol. Grade: 90%. CAS No. 108102-51-8. Molecular formula: C16H26O4. Mole weight: 282.38. BOC Sciences 8
Fumagillol Fumagillol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: FUMAGILLOL. Product Category: Heterocyclic Organic Compound. CAS No. 35903-52-7. Molecular formula: C16H26O4. Mole weight: 282.38. Product ID: ACM35903527. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 5
TNP-470 (AGM-1470, O-(Chloroacetyl-carbamoyl)fumagillol, AGM1470, MetAP-2 Inhibitor II, MetAP2 Inhibitor II, Methionine Aminopeptidase 2 Inhibitor II, TNP470) A cell-permeable Fumagillin analog that inhibits MetAP2, but not MetAP1, methionine aminopeptidase activity (IC50 = 1nM against human MetAP2), without affecting the inhibitory activity of MetAP2 against HRI- (heme-regulated inhibitor kinase) catalyzed eIF-2alpha phosphorylation. A potent endothelial cytostasis inducer (IC50 = 25 pM and 37 pM, respectively, against HUVEC and bovine BAEC) in vitro and an effective anti-angiogenesis agent in vivo (2-100mg/kg in mice and rats; s.c.). Group: Biochemicals. Grades: Highly Purified. CAS No. 129298-91-5. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 4
Worldwide
AUTAC1 AUTAC1 is a MetAP2-targeting autophagy-mediated degrader (AUTAC), which contains a degradation tag and a warhead to provide target specificity. It is composed of an FBnG (p-Fluorobenzyl Guanine) and a Fumagillol moiety, with the Fumagillol binding covalently to MetAP2. AUTAC1 has potential anticancer activity as it can degrade MetAP2 and FKBP12 proteins and is used in the synthesis of PROTACs. This compound represents a novel targeted-clearance strategy that harnesses the autophagy-lysosome pathway for the degradation of specific proteins, expanding the scope of targeted protein degradation beyond the limitations of proteasomal clearance. Synonyms: (3R,4S,5S,6R)-5-Methoxy-4-((2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl)-1-oxaspiro[2.5]octan-6-yl ((R)-4-(((2-amino-9-(4-fluorobenzyl)-6-oxo-6,9-dihydro-1H-purin-8-yl)thio)methyl)-2,5-dioxo-10,13,16-trioxa-3,6-diazanonadecan-19-yl)carbamate; 6,9,12-Trioxa-2,16,19-triazaheneicosanoic acid, 18-[[[2-amino-9-[(4-fluorophenyl)methyl]-6,9-dihydro-6-oxo-1H-purin-8-yl]thio]methyl]-17,20-dioxo-. Grade: ≥95%. CAS No. 2241669-09-8. Molecular formula: C44H63FN8O11S. Mole weight: 931.08.… BOC Sciences 6
Beloranib Beloranib is an experimental drug candidate for the treatment of obesity. It was discovered by CKD Pharmaceuticals and is currently being developed by Zafgen. Beloranib, an analog of the natural chemical compound fumagillin, is an inhibitor of the enzyme METAP2. It was originally designed as angiogenesis inhibitor for the treatment of cancer. Uses: Angiogenesis inhibitors. Synonyms: 2-Propenoic acid, 3-[4-[2-(dimethylamino)ethoxy]phenyl]-, (3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]oct-6-yl ester, (2E)-; CDK-732; CDK 732; CDK732; O-[4-(2-Dimethylaminoethoxy)-trans-cinnamoyl]fumagillol; 2-Propenoic acid, 3-[4-[2-(dimethylamino)ethoxy]phenyl]-, (3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-1-oxaspiro[2.5]oct-6-yl ester, (2E)-; ZGN 440. Grade: ≥95%. CAS No. 251111-30-5. Molecular formula: C29H41NO6. Mole weight: 499.64. BOC Sciences 6
Evexomostat Evexomostat is a methionine aminopeptidase 2 (MetAP2) inhibitor. Synonyms: poly({N-[(2RS)-2-hydroxypropyl]methacrylamide}-co-[N-methacryloylgly-cyl-L-phenylalanyl-L-leucyl-N1-(trans-4-{[({(3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]-octan-6-yl}oxy)carbonyl]amino}cyclohexyl)glycinamide (~0.91:0.09 x)]); poly([N-(2-hydroxypropyl)methacrylamide]-co-{methacryloyl-Gly-Phe-Leu-Gly amide with O-[(trans-4-aminocyclohexyl)carbamoyl]fumagillol}). CAS No. 2416263-67-5. Molecular formula: [(C7H13NO2)n(C46H68N6O10)]m. BOC Sciences 8

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