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SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT

Product Name
SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT
CAS No.
98672-91-4
Chemical Name
SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT
Synonyms
BMS-18290;RJNDVCNWVBWHLY-BHQIHCQQSA-N;SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT;1S-[1α,2β(5Z),3β,4α]]-7-[3-[2-(Phenylcarbamoyl)hydrazinomethyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoic acid;(Z)-7-[(1R,4S)-3α-[[2-[(Phenylamino)carbonyl]hydrazino]methyl]-7-oxabicyclo[2.2.1]heptan-2α-yl]-5-heptenoic acid;1S-[1α,2α(Z),3α,4α]]-7-[3-[[2-[(phenylamino)carbonyl]hydrazino]methyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoicacid;5-Heptenoic acid, 7-[(1S,2R,3R,4R)-3-[[2-[(phenylamino)carbonyl]hydrazinyl]methyl]-7-oxabicyclo[2.2.1]hept-2-yl]-, (5Z)-
CBNumber
CB8504564
Molecular Formula
C21H29N3O4
Formula Weight
387.47
MOL File
98672-91-4.mol
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SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT Property

Melting point:
92-95 °C
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
≤0.9mg/ml in ethanol;5mg/ml in DMSO;0.14mg/ml in dimethyl formamide
form 
White to off-white crystalline powder.
pka
4.76±0.10(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
19025
Product name
SQ 29,548
Purity
≥98%
Packaging
1mg
Price
$85
Updated
2024/03/01
Cayman Chemical
Product number
19025
Product name
SQ 29,548
Purity
≥98%
Packaging
5mg
Price
$383
Updated
2024/03/01
Cayman Chemical
Product number
19025
Product name
SQ 29,548
Purity
≥98%
Packaging
10mg
Price
$680
Updated
2024/03/01
TRC
Product number
S683703
Product name
SQ-29548
Packaging
1mg
Price
$1200
Updated
2021/12/16
ApexBio Technology
Product number
C4237
Product name
SQ29,548
Packaging
10mg
Price
$720
Updated
2021/12/16
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SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT Chemical Properties,Usage,Production

Description

SQ 29,548 is a highly selective TP receptor antagonist which binds to the human recombinant TP receptor with a Ki of 4.1 nM. It inhibits the aggregation of washed human platelets induced by U-46619 with an IC50 of 0.06 μM. It antagonizes U-46619 induced contraction of rat and guinea pig tracheal, arterial, and venous smooth muscles with drug/receptor dissociation constants (KB) in the range of 0.5-1.7 nM. SQ 29,548 also inhibits the contraction of rat vascular smooth muscle induced by 8-iso PGF.

Uses

SQ-29548 is a potent and selective thromboxane A2 receptor antagonist.

in vitro

in guinea-pig trachea and rat aorta, sq 29,548 competitively antagonized the activity of 9,11-azo pgh2 with pa2 values of 7.8 and 8.4, respectively. sq 29,548 competitively antagonized contractions of guinea-pig tracheal spirals induced by 11,9-epoxymethano pgh2 with the pa2 value of 9.1. the sq 29,548 competitively antagonized tracheal induced by 11,9-epoxymethano pgh2 and pgd2 with the pa2 values of 8.2 and 8.3, respectively. sq 29,548 partially antagonized the contractions of guinea-pig tracheal spirals caused by pge2. sq 29,548 significantly inhibited the aorta contracting activity of 11,9-epoxymethano pgh2 (pa2 = 9.1) and thromboxane a2 released from perfused guinea-pig lungs upon arachidonic acid challenge [1].

in vivo

in anesthetized dogs, sq 29,548 (0.2 mg/kg/h) completely inhibited the vasoconstrictor response of the left circumflex coronary artery (lcx) caused by u-46619. sq 28,585 showed no effects on infarct size as compared with vehicle controls [3]. in sham mi rats, treatment with sq-29,548 significantly blunted this loss of ck activity and amino-nitrogen concentration from the ischemic myocardium. sq-29,548 significantly prevented the extension of ischemic damage in the myocardium and improved survival following acute coronary artery ligation [4].

References

[1] ogletree m l, harris d n, greenberg r, et al. pharmacological actions of sq 29,548, a novel selective thromboxane antagonist[j]. journal of pharmacology and experimental therapeutics, 1985, 234(2): 435-441.
[2] abe t, takeuchi k, takahashi n, et al. rat kidney thromboxane receptor: molecular cloning, signal transduction, and intrarenal expression localization[j]. journal of clinical investigation, 1995, 96(2): 657.
[3] grover g j, schumacher w a. effect of the thromboxane receptor antagonist sq 29,548 on myocardial infarct size in dogs[j]. journal of cardiovascular pharmacology, 1988, 11(1): 29-35.
[4] hock c e, brezinski m e, lefer a m. anti-ischemic actions of a new thromboxane receptor antagonist, sq-29,548, in acute myocardial ischemia[j]. european journal of pharmacology, 1986, 122(2): 213-219.

SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT Preparation Products And Raw materials

Raw materials

Preparation Products

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SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT Suppliers

Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11289
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Shanghai Universal Biotech Co.,Ltd
Tel
18768175414
Email
gaojun@univ-bio.com
Country
China
ProdList
24998
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58
Aladdin Scientific
Tel
+1-833-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
52927
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58

98672-91-4, SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPTRelated Search:


  • SQ 29,548 (POTENT AND SPECIFIC THROMBOXA NE A2 RECEPT
  • (Z)-7-[(1R,4S)-3α-[[2-[(Phenylamino)carbonyl]hydrazino]methyl]-7-oxabicyclo[2.2.1]heptan-2α-yl]-5-heptenoic acid
  • BMS-18290
  • 1S-[1α,2β(5Z),3β,4α]]-7-[3-[2-(Phenylcarbamoyl)hydrazinomethyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoic acid
  • RJNDVCNWVBWHLY-BHQIHCQQSA-N
  • 5-Heptenoic acid, 7-[(1S,2R,3R,4R)-3-[[2-[(phenylamino)carbonyl]hydrazinyl]methyl]-7-oxabicyclo[2.2.1]hept-2-yl]-, (5Z)-
  • 1S-[1α,2α(Z),3α,4α]]-7-[3-[[2-[(phenylamino)carbonyl]hydrazino]methyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoicacid
  • 98672-91-4