Bryostatin 1
CAS No. 83314-01-6
Bryostatin 1( NSC 339555 | Bryostatin1 )
Catalog No. M16088 CAS No. 83314-01-6
Bryostatin 1 (NSC 339555) is a macrocyclic lactone derived from a marine invertebrate, fuctions as an activator of PKC with high binding affinity (Ki=1.35 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
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Biological Information
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Product NameBryostatin 1
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NoteResearch use only, not for human use.
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Brief DescriptionBryostatin 1 (NSC 339555) is a macrocyclic lactone derived from a marine invertebrate, fuctions as an activator of PKC with high binding affinity (Ki=1.35 nM).
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DescriptionBryostatin 1 (NSC 339555) is a macrocyclic lactone derived from a marine invertebrate, fuctions as an activator of PKC with high binding affinity (Ki=1.35 nM); functions like the phorbol esters biochemically in binding to and activating protein kinase C; inhibits tumor promotion by phorbol esters in SENCAR mouse skin, induces differentiation of B-chronic lymphocytic leukemia cells; blocks phorbol ester action in Friend cells, restores the differentiation respons with EC50 of 15 nM.Alzheimer Disease Phase 2 Clinical.
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In VitroBryostatin 1 (1 μM; 5 minutes; HT22 cells) treatment successfully recruits Munc13-1 from the cytosol to the plasma membrane. Effects of Bryostatin 1 on the other Munc13 family members, ubMunc13-2 and bMunc13-2, resembled those of Munc13-1 for translocation .The increased level of expression of Munc13-1 following a 24 h incubation with Bryostatin 1 in both HT22 and primary mouse hippocampal cells is observed.Bryostatin 1 can also affect the immune system by modulating dendritic cells (DCs) via toll-like receptor 4 (TLR4) through the MyD88-independent pathway, which favors an anti-inflammatory environment by inducing a type 2 phenotype that promotes the differentiation of CD4+ T-helper (Th) lymphocytes into Th2 versus Th1 effector cells. Western Blot Analysis Cell Line:HT22 cells Concentration:1 μM Incubation Time:5 minutes Result:Caused Munc13-1 to transfer to the membrane fraction.
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In VivoBryostatin 1 (30 μg/kg; intraperitoneal injection; 3 d per week; for 2 weeks; C57BL/6J mice) treatment abolishes the onset of EAE. Animal Model:Female C57BL/6J mice (8-12-week-old) with MOG35-55 Dosage:30 μg/kg Administration:Intraperitoneal injection; 3 d per week; for 2 weeks Result:Abolished the onset of experimental autoimmune encephalomyelitis (EAE).
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SynonymsNSC 339555 | Bryostatin1
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PathwayAngiogenesis
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TargetPKC
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RecptorPKC
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number83314-01-6
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Formula Weight905.044
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Molecular FormulaC47H68O17
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Purity>98% (HPLC)
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Solubility——
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SMILESCCC/C=C/C=C/C(O[C@@H](/C(C[C@@](O1)([H])C[C@H]([C@H](O)C)O2)=C/C(OC)=O)[C@]1(O)C(C)(C)/C=C/[C@@](O3)([H])C/C(C[C@@]3([H])C[C@@](O4)(O)C(C)(C)[C@@H](OC(C)=O)C[C@@]4([H])C[C@@H](O)CC2=O)=C\C(OC)=O)=O
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Chemical Name2,4-Octadienoic acid, 25-(acetyloxy)-1,11,21-trihydroxy-17-(1-hydroxyethyl)-5,13-bis(2-methoxy-2-oxoethylidene)-10,10,26,26-tetramethyl-19-oxo-18,27,28,29-tetraoxatetracyclo[21.3.1.13,7.111,15]nonacos-8-en-12-yl ester, [1S-[1R*,3R*,5Z,7S*,8E,11R*,12R*(2E,
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Rottlerin
Rottlerin (Mallotoxin;NSC 94525) is a polyphenol natural product, cell-permeable and reversible PKC inhibitor that exhibits greater selectivity for PKCδ (IC50=3-6 uM) and PKCθ.
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PKC-IN-7
PKC-IN-7 is a potent, selective, reversible, ATP-competitive PKCα/β inhibitor with IC50 of 4.7/3.3 nM.
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PKC β pseudosubstrat...
Selective cell-permeable peptide inhibitor of protein kinase C (IC50 ~ 0.5 μM). Consists of amino acids 19 - 31 of PKC pseudosubstrate domain linked by a disulphide bridge to a cell permeabilisation Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the inhibitor peptide. Once inside the cell, the disulphide bonds are subjected to reduction in the cytoplasm leading to release of the inhibitor peptide.
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