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(2R)-2-cyclopentyl-2-[4-(quinolin-2-ylmethoxy)phenyl]acetic acid

(2R)-2-cyclopentyl-2-[4-(quinolin-2-ylmethoxy)phenyl]acetic acid structure

CAS No:
128253-31-6
Formula:
C23H23NO3
Chemical Name:
(2R)-2-cyclopentyl-2-[4-(quinolin-2-ylmethoxy)phenyl]acetic acid
Synonyms:
2-(4-(quinolin-2-yl-methoxy)phenyl)-2-cyclopentylacetic acid;Bay X 1005;Bay X1005;Bay-X1005;BAYX-1005;DG-031;Veliflapon;Veliflapon;128253-31-6;Bay-x-1005;Bay X 1005;DG-031;Bay-X1005;BAY 1005;UNII-JXH6X663L0;BAY-X 1005;DG 031;CHEMBL88712;JXH6X663L0;(2R)-2-cyclopentyl-2-[4-(quinolin-2-ylmethoxy)phenyl]acetic acid;128253-31-6 (acid);Bayx-1005;Bay X1005;(2R)-cyclopentyl{4-[(quinolin-2-yl)methoxy]phenyl}acetic acid;(R)-2-(4-(Quinolin-2-yl-methoxy)phenyl)-2-cyclopentylacetic acid;Veliflapon [USAN:INN];Velifapon;2-(4-(quinolin-2-yl-methoxy)phenyl)-2-cyclopentylacetic acid;QY1;Veliflapon (USAN/INN);Benzeneacetic acid, alpha-cyclopentyl-4-(2-quinolinylmethoxy)-, (R)-;MLS006010705;GTPL5148;SCHEMBL1004174;BAY-X-005;DTXSID60155843;ZINC598193;BDBM50052030;MFCD00870329;AKOS024457673;SB19085;NCGC00250411-01;HY-14165;SMR004701678;CS-0003243;BAY-X-1005, >=98% (HPLC);D06664;Q27074919;Cyclopentyl-[4-(quinolin-2-ylmethoxy)-phenyl]-acetic acid;(R)-?-Cyclopentyl-4-(2-quinolinylmethoxy)benzeneacetic acid;(R)-Cyclopentyl-[4-(quinolin-2-ylmethoxy)-phenyl]-acetic acid;2-(R)-cyclopentyl-2-(4-(2-quinolylmethoxy)phenyl)acetic acid;(r)-2-[4-(quinolin-2-yl-methoxy)phenyl]-2-cyclopentyl acetic acid;alpha-Cyclopentyl-4-(2-quinolinylmethoxy)-(R)-benzeneacetic acid;(alphaR)-alpha-Cyclopentyl-4-(2-quinolinylmethoxy)-benzeneacetic acid

Description

Veliflapon is under investigation in clinical trial NCT00353067 (Veliflapon (Dg-031)to Prevent Heart Attacks or Stroke in Patients With a History of Heart Attack or Unstable Angina).

(2R)-2-cyclopentyl-2-[4-(quinolin-2-ylmethoxy)phenyl]acetic acid Basic Attributes

Molecular Weight：

361.4 g/mol

Exact Mass：

361.16779360 g/mol

UNII：

JXH6X663L0

DSSTox ID：

DTXSID60155843

Characteristics

PSA：

59.4 Å²

Drug Information

MeSH：

Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)|Compounds that bind to and inhibit that enzymatic activity of LIPOXYGENASES. Included under this category are inhibitors that are specific for lipoxygenase subtypes and act to reduce the production of LEUKOTRIENES. (See all compounds classified as Lipoxygenase Inhibitors.)

MeSH Entry Terms：

2-(4-(quinolin-2-yl-methoxy)phenyl)-2-cyclopentylacetic acid

Computed Properties

Molecular Weight:361.4
XLogP3:5.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:361.16779360
Monoisotopic Mass:361.16779360
Topological Polar Surface Area:59.4
Heavy Atom Count:27
Complexity:482
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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Guide of (2R)-2-cyclopentyl-2-[4-(quinolin-2-ylmethoxy)phenyl]acetic acid

Description
Basic Attributes
Characteristics
Drug Information
Computed Properties
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