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SML0278

SR 48692

Name: SR 48692
Brand: SIGMA

≥98% (HPLC), nonpeptide NT1 neurotensin receptor antagonist , powder

别名:

2-[[[1-(7-Chloro-4-quinolinyl)-5-(2,6-dimethoxyphenyl)-1H-pyrazol-3-yl]carbonyl]amino]-tricyclo[3.3.1.13,7]decane-2-carboxylic acid, Meclinertant

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关于此项目

经验公式（希尔记法）:

C₃₂H₃₁ClN₄O₅

化学文摘社编号:

146362-70-1

分子量:

587.07

UNSPSC Code:

12352200

PubChem Substance ID:

329825286

NACRES:

NA.77

Assay:

≥98% (HPLC)

Form:

powder

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属性

产品名称

SR 48692, ≥98% (HPLC)

Quality Segment

100

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: ≥2 mg/mL (warmed)

storage temp.

−20°C

SMILES string

COc1cccc(OC)c1-c2cc(nn2-c3ccnc4cc(Cl)ccc34)C(=O)NC5(C6CC7CC(C6)CC5C7)C(O)=O

InChI

1S/C32H31ClN4O5/c1-41-27-4-3-5-28(42-2)29(27)26-16-24(36-37(26)25-8-9-34-23-15-21(33)6-7-22(23)25)30(38)35-32(31(39)40)19-11-17-10-18(13-19)14-20(32)12-17/h3-9,15-20H,10-14H2,1-2H3,(H,35,38)(H,39,40)

InChI key

DYLJVOXRWLXDIG-UHFFFAOYSA-N

Gene Information

human ... NTSR1(4923)

说明

Application

SR 48692 has been used as a neurotensin high-affinity receptor 1 (NTSR1) antagonist:

to explore the function of NTSR1 in glioblastoma (GBM) cells
to determine the roles of neurotensin (NT) in the regulation of bile acid (BA) uptake, in vivo
to explore the involvement of NTSR1 versus NTSR2 in mice

Biochem/physiol Actions

SR 48692 is a high affinity, orally bioavailable and selective nonpeptide NT1 neurotensin receptor antagonist that antagonizes neurotensin-induced calcium mobilization with a pA2 of 8.13 in HT-29 human colon carcinoma cell line, and blocks the ability of neurotensin to increase GABA levels in the prefrontal cortex.

SR 48692 is a high affinity, orally bioavailable and selective nonpeptide NT1 neurotensin receptor antagonist.

Features and Benefits

This compound is featured on the Neurotensin Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

存储类别

11 - Combustible Solids

怎么回事？

WGK 3

闪点 (F)

Not applicable

闪点 (°C)