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Merck

M7068

Sigma-Aldrich

MPP 二盐酸盐 水合物

≥97% (HPLC), powder, estrogen receptor α agonist

别名:

1,3-双(4-羟基苯基)-4-甲基-5-[4-(2-哌啶基乙氧基)苯酚]-1H-吡唑二盐酸盐 水合物, 甲基哌啶基吡唑 水合物

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About This Item

经验公式(希尔记法):
C29H31N3O3 · 2 HCl · xH2O
分子量:
542.50 (anhydrous basis)
MDL號碼:
分類程式碼代碼:
51111800
PubChem物質ID:
NACRES:
NA.77

product name

MPP 二盐酸盐 水合物, ≥97% (HPLC), white, powder

品質等級

化驗

≥97% (HPLC)

形狀

powder

儲存條件

desiccated

顏色

white

溶解度

DMSO: soluble ≥20 mg/mL

SMILES 字串

Cl.Cl.Cc1c(nn(-c2ccc(O)cc2)c1-c3ccc(OCCN4CCCCC4)cc3)-c5ccc(O)cc5

InChI

1S/C29H31N3O3.2ClH/c1-21-28(22-5-11-25(33)12-6-22)30-32(24-9-13-26(34)14-10-24)29(21)23-7-15-27(16-8-23)35-20-19-31-17-3-2-4-18-31;;/h5-16,33-34H,2-4,17-20H2,1H3;2*1H

InChI 密鑰

FWDNPWVVRVSJQH-UHFFFAOYSA-N

一般說明

甲基-哌啶基-吡唑水合物(MPP)可由甲基-吡唑-三醇(MPT)(一种吡唑三醇)进行制备。

應用

MPP二盐酸盐水合物已在下列研究中被用作雌激素受体α拮抗剂:
  • 用于人乳腺癌MCF-7细胞中
  • 预处理子宫内膜 离体 器官培养(EVOC)
  • 处理垂体以监测促黄体激素的分泌

生化/生理作用

MPP 二盐酸盐是一种特异性雌激素受体 α拮抗剂。
甲基-哌啶基-吡唑水合物(MPP)是一种雌激素受体α激动剂,其缺乏雌激素受体(ER)的配体功能β。它可促进水飞蓟宾诱导的人乳腺癌MCF-7细胞凋亡。

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

dust mask type N95 (US), Eyeshields, Gloves


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Nan Zheng et al.
Journal of pharmacological sciences, 128(3), 97-107 (2015-06-29)
The estrogen receptor alpha (ERα) has been proven to be one of the most important therapeutic targets in breast cancer over the last 30 years. Previous studies pointed out that a natural flavonoid, silibinin, induced apoptosis in human breast cancer
Fu Guangtao et al.
Frontiers in pharmacology, 12, 746391-746391 (2021-11-23)
Periprosthetic osteolysis is one of the major long-term complications following total joint replacement. Its cause is widely accepted to be wear particle-induced activation of inflammatory macrophages. No effective strategy for the prevention and treatment of periprosthetic osteolysis is yet available.
Hai-Bing Zhou et al.
Bioorganic & medicinal chemistry letters, 19(1), 108-110 (2008-11-19)
Methyl-piperidino-pyrazole (MPP), an estrogen receptor alpha (ERalpha)-selective antagonist we developed, has a basic side chain (BSC) attached to an ERalpha-selective agonist ligand, methyl-pyrazole-triol (MPT) through an ether linkage. To remove the possibility that metabolic cleavage of the BSC in MPP
Julia Y H Liu et al.
General and comparative endocrinology, 272, 63-75 (2018-12-06)
Estrogen is well known to have a modulatory role on gastrointestinal tract, particularly through its interaction with nuclear estrogen receptors (ERs), alpha and beta (ERα/β). Recent functional studies also indicate that estrogen can activate a G-protein coupled estrogen receptor, GPR30
João P E Saut et al.
Reproduction (Cambridge, England), 148(6), 593-606 (2014-09-24)
The risk of bacterial infection of the endometrium causing uterine disease in cattle is increased in the progesterone-dominated luteal phase of the ovarian cycle, while oestrogens or oestrus are therapeutic or protective against disease. The first line of defence against

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