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Merck

B7431

Sigma-Aldrich

Bryostatin 1

≥99%, solid

Sinónimos:

NSC 339555

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About This Item

Fórmula empírica (notación de Hill):
C47H68O17
Número de CAS:
Peso molecular:
905.03
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.77
En este momento no podemos mostrarle ni los precios ni la disponibilidad

Nivel de calidad

Ensayo

≥99%

Formulario

solid

color

white

solubilidad

DMSO: soluble
ethanol: soluble

temp. de almacenamiento

−20°C

cadena SMILES

[H]\C(C(=O)OC)=C1/C[C@@]2([H])C[C@]3(O)O[C@]([H])(C[C@@H](O)CC(=O)O[C@H](C[C@]4([H])C\C(=C(\[H])C(=O)OC)[C@H](OC(=O)\C=C\C=C\CCC)[C@@](O)(O4)C(C)(C)\C=C\[C@@]([H])(C1)O2)[C@@H](C)O)C[C@H](OC(C)=O)C3(C)C

InChI

1S/C47H68O17/c1-10-11-12-13-14-15-39(51)62-43-31(22-41(53)58-9)21-34-25-37(28(2)48)61-42(54)24-32(50)23-35-26-38(59-29(3)49)45(6,7)46(55,63-35)27-36-19-30(20-40(52)57-8)18-33(60-36)16-17-44(4,5)47(43,56)64-34/h12-17,20,22,28,32-38,43,48,50,55-56H,10-11,18-19,21,23-27H2,1-9H3/b13-12+,15-14+,17-16+,30-20+,31-22+/t28-,32-,33+,34+,35-,36+,37-,38+,43+,46+,47-/m1/s1

Clave InChI

MJQUEDHRCUIRLF-TVIXENOKSA-N

Aplicación

Bryostatin 1 has been used to study its effects on spontaneous Crohn′s disease (CD) like colitis in mice.[1] It has also been used to study its effects as an anthelmintic drug on adult Syphacia muris infection in rats.[2]

Acciones bioquímicas o fisiológicas

Bryostatin 1 (Bry1) is a macrocyclic lactone.[3] This synaptogenic compound[4] is obtained from the marine bryozoan Bugula neritina.[1] Bry1 is capable of reversing synaptic loss. It can enable synaptic maturation in animal models with several neurological disorders.[3] It possesses antidepressant activity, when administered intracebroventricularly.[4] Bry1 is known to participate in protecting cell tight junctions (TJs), anti-inflammatory functions and immune regulation.[1]
Macrolactone isolated from the marine bryozoan Bugula neritina that initially activates and subsequently down-regulates protein kinase C (PKC). More potent than phorbol myristate acetate for translocating PKCδ and ε.

Otras notas

Binds to glass and plastic in aqueous solutions

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Tonia J Buchholz et al.
Chemistry & biology, 17(10), 1092-1100 (2010-11-03)
In vitro analysis of natural product biosynthetic gene products isolated from unculturable symbiotic bacteria is necessary to probe the functionalities of these enzymes. Herein, we report the biochemical characterization of BryR, the 3-hydroxy-3-methylglutaryl (HMG)-CoA synthase (HMGS) homolog implicated in β-branching at
Robert J Morgan et al.
Investigational new drugs, 30(2), 723-728 (2010-10-12)
The California Cancer Consortium has performed a Phase II trial of infusional bryostatin, a protein kinase C inhibitor isolated from the marine invertebrate bryozoan, Bugula Neritina, a member of the phylum Ectoprocta, in combination with cisplatin, in patients (pts) with
Gary E Keck et al.
Bioorganic & medicinal chemistry letters, 22(12), 4084-4088 (2012-05-15)
The role of the C(8) gem-dimethyl group in the A-ring of bryostatin 1 has been examined through chemical synthesis and biological evaluation of a new analogue. Assays for biological function using U937, K562, and MV4-11 cells as well as the
Signaling pathways involved in cognitive enhancement
Cognition, 11-42 (2015)
H Kim et al.
Neuroscience, 226, 348-355 (2012-09-19)
Activation of protein kinase C (PKC) by bryostatin-1 affects various functions of the central nervous system. We explored whether bryostatin-1 influenced synaptic plasticity via a process involving PKC. Our purpose was to examine whether bryostatin-1 affected the induction of hippocampal

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