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1-[4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-biphenyl]-4-yl]cyclopropane-1-carboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1380587-40-5

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1380587-40-5 Usage

Molecular weight

428.2 g/mol

Cyclopropane ring

A three-membered carbon ring

Carboxylic acid group

A -COOH group

Ethyl ester group

An -COOEt group

Substituted biphenyl group

A biphenyl with a 4'-yl group substitution

Dioxaborolan-2-yl group

A boron-containing group with a 1,3,2-dioxaborole structure

Structural features

The molecule consists of a cyclopropane ring fused to a substituted biphenyl group
The biphenyl group has a 4'-yl substitution, which is connected to the cyclopropane ring
The carboxylic acid group is attached to the cyclopropane ring
The ethyl ester group is connected to the carboxylic acid group
The dioxaborolan-2-yl group is attached to the biphenyl group

Pharmaceutical research

Due to its complex structure, it may have the potential to manipulate biological pathways

Chemical research

It could serve as a building block for the synthesis of other compounds

Solubility

Likely soluble in organic solvents such as dichloromethane, ethyl acetate, and acetone

Stability

Stable under normal laboratory conditions, but sensitive to moisture and air due to the presence of the boron-containing group

Reactivity

May undergo reactions such as hydrolysis, esterification, and Suzuki-Miyaura cross-coupling reactions due to the presence of various functional groups

Purity

Typically synthesized with high purity, but may require purification techniques such as column chromatography or recrystallization to remove impurities

Safety precautions

Handle with care, as the compound may be toxic or harmful if ingested, inhaled, or absorbed through the skin. Use appropriate personal protective equipment (PPE) and follow proper disposal procedures.

Check Digit Verification of cas no

The CAS Registry Mumber 1380587-40-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,8 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1380587-40:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*8)+(3*7)+(2*4)+(1*0)=175
175 % 10 = 5
So 1380587-40-5 is a valid CAS Registry Number.

1380587-40-5Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLE COMPOUNDS AS LPAR ANTAGONISTS

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, (2014/01/09)

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of inflammatory diseases and disorders such as, for example, pulmonary fibrosis

LYSOPHOSPHATIDIC ACID RECEPTOR ANTAGONISTS AND USES THEREOF

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Page/Page column 127, (2012/06/30)

Described herein are compounds that are antagonists of lysophosphatidic receptor(s). Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well as methods of using such antagonists, alone and in combination with other compounds, for treating LPA-dependent or LPA-mediated conditions or diseases.

Discovery of highly selective and orally active lysophosphatidic acid receptor-1 antagonists with potent activity on human lung fibroblasts

Qian, Yimin,Hamilton, Matthew,Sidduri, Achyutharao,Gabriel, Stephen,Kondru, Rama,Narayanan, Arjun,Lucas, Matthew,Schoenfeld, Ryan C.,Laine, Dramane,Ren, Yonglin,Peng, Ruoqi,Chang, Kung-Ching,Fuentes, Maria E.,Stevenson, Christopher S.,Budd, David C.,Truitt, Terry,Hamid, Rachid,Chen, Yun,Zhang, Lin,Fretland, Adrian J.,Sanchez, Ruben Alvarez

, p. 7920 - 7939,20 (2020/08/24)

Lysophosphatidic acid is a class of bioactive phospholipid that mediates most of its biological effects through LPA receptors, of which six isoforms have been identified. The recent results from LPA1 knockout mice suggested that blocking LPA1 signaling could provide a potential novel approach for the treatment of idiopathic pulmonary fibrosis. Here, we report the design and synthesis of pyrazole- and triazole-derived carbamates as LPA1-selective and LPA1/3 dual antagonists. In particular, compound 2, the most selective LPA1 antagonist reported, inhibited proliferation and contraction of normal human lung fibroblasts (NHLF) following LPA stimulation. Oral dosing of compound 2 to mice resulted in a dose-dependent reduction of plasma histamine levels in a murine LPA challenge model. Furthermore, we applied our novel antagonists as chemistry probes and investigated the contribution of LPA1/2/3 in mediating the pro-fibrotic responses. Our results suggest LPA1 as the major receptor subtype mediating LPA-induced proliferation and contraction of NHLF.

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