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Merck

B7431

Sigma-Aldrich

苔藓抑素1

≥99%, solid

别名:

NSC 339555

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About This Item

经验公式(希尔记法):
C47H68O17
CAS号:
分子量:
905.03
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥99%

形狀

solid

顏色

white

溶解度

DMSO: soluble
ethanol: soluble

儲存溫度

−20°C

SMILES 字串

[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

InChI 密鑰

MJQUEDHRCUIRLF-TVIXENOKSA-N

應用

苔藓虫素1已用于研究其对小鼠结肠炎等自发性克罗恩病′(CD)的影响。它也已用于研究其作为驱虫药对大鼠中成年鼠管线虫感染的影响。

生化/生理作用

苔藓虫素(Bry1)是一种大环内酯。这种突触发生性化合物是从海洋苔藓虫多室草苔虫中获得的。Bry1能够逆转突触损失。它可以促进多种神经系统疾病动物模型中的突触成熟。当用于脑室给药时,它具有抗抑郁活性。现已确知Bry1参与保护细胞紧密连接(TJ)、抗炎功能和免疫调节。
从海洋苔藓虫 Bugula neritina 中分离的大环内酯可首先激活并随后下调蛋白激酶C(PKC)。其转移PKCδ 和ε的效果比佛波醇肉豆蔻酸乙酸酯更好。

其他說明

与水溶液中的玻璃和塑料结合

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Yasuyuki Ogawa et al.
The Journal of organic chemistry, 78(1), 104-115 (2012-11-06)
The Prins cyclization of syn-β-hydroxy allylsilanes and aldehydes gives cis-2,6-disubstituted 4-alkylidenetetrahydropyrans as sole products in excellent yields regardless of the aldehyde (R″) or syn-β-hydroxy allylsilane substituent (R') used. By reversing the R″ and R' groups, complementary exocyclic stereocontrol can be
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
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
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

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