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PIRIPROST POTASSIUM SALT

CAS No.
88851-62-1
Chemical Name:
PIRIPROST POTASSIUM SALT
Synonyms
U-60257B;U60,257B POTASSIUM SALT;PIRIPROST POTASSIUM SALT;potassium:5-[(4R,5R)-5-hydroxy-4-[(E,3S)-3-hydroxyoct-1-enyl]-1-phenyl-5,6-dihydro-4H-cyclopenta[b]pyrrol-2-yl]pentanoate;1,4(R),5(R),6-TETRAHYDRO-5-HYDROXY-4-[(1E,3S)-HYDROXY-1-OCTENYL]-1-PHENYL-CYCLOPENTA[B]PYRROLE-2-PENTANOIC ACID, MONOPOTASSIUM SALT;[4R-[4A(1E,3S*),5B]]-1,4,5,6-TETRAHYDRO-5-HYDROXY-4-(3-HYDROXY-1-OCTENYL)-1-PHENYL-CYCLOPENTA[B]PYRROLE-2-PENTANOIC ACID, POTASSIUM SALT;[4r-[4α(1e,3s*),5β]]-1,4,5,6-tetrahydro-5-hydroxy-4-(3-hydroxy-1-octenyl)-1-phenyl-cyclopenta[b]pyrrole-2-pentanoic acid, potassium salt;U60,257B, [4R-[4α(1E,3S*),5β]]-1,4,5,6-Tetrahydro-5-hydroxy-4-(3-hydroxy-1-octenyl)-1-phenyl-cyclopenta[b]pyrrole-2-pentanoic acid, potassium salt
CBNumber:
CB3199257
Molecular Formula:
C26H34KNO4
Molecular Weight:
463.65
MDL Number:
MFCD02259346
MOL File:
88851-62-1.mol
Last updated:2023-05-18 11:31:06

PIRIPROST POTASSIUM SALT Properties

storage temp. −20°C
solubility ≤43mg/ml in ethanol;30mg/ml in DMSO;8.6mg/ml in dimethyl formamide
form solid
FDA UNII 2ZYM2BH34M

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3

PIRIPROST POTASSIUM SALT price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 18228 Piriprost (potassium salt) ≥98% 88851-62-1 1mg $53 2024-03-01 Buy
Cayman Chemical 18228 Piriprost (potassium salt) ≥98% 88851-62-1 5mg $227 2024-03-01 Buy
Cayman Chemical 18228 Piriprost (potassium salt) ≥98% 88851-62-1 10mg $399 2024-03-01 Buy
Cayman Chemical 18228 Piriprost (potassium salt) ≥98% 88851-62-1 50mg $1740 2024-03-01 Buy
TRC P508803 PiriprostPotassium 88851-62-1 2.5mg $135 2021-12-16 Buy
Product number Packaging Price Buy
18228 1mg $53 Buy
18228 5mg $227 Buy
18228 10mg $399 Buy
18228 50mg $1740 Buy
P508803 2.5mg $135 Buy

PIRIPROST POTASSIUM SALT Chemical Properties,Uses,Production

Uses

Piriprost Potassium is a structural analog of prostaglandin I2.

Uses

Antiasthmatic.

Biological Activity

piriprost (u 60257) is a leukotriene synthesis inhibitor [1].leukotrienes belong to a family of eicosanoid inflammatory mediators produced in leukocytes. leukotrienes mainly act on a subfamily of g protein-coupled receptors. the production of leukotrienes is implicated in triggerring contractions in the smooth muscles lining the bronchioles and is a major cause of inflammation in asthma and allergic rhinitis [2].piriprost inhibited the formation of 5-hydroxyeicosatetraenoic acid (5-hete), ltb4, and the sulfidopeptide leukotrienes with the ic50 values ranged from 9 to 14 μm for the mouse mast cells and 15-50 μm for the basophil leukemia cells. piriprost weakly inhibited the solubilized ltc synthase of rat basophil leukemia cells with the ic50 of 1.5 mm [1]. piriprost increased alkaline phosphatase (alp) activity in cultured endometrial stromal cells. piriprost (100 μm) inhibited 5-lipoxygenase activity and decreased 5-hydroxy-eicosatetraenoic acid (a 5-lipoxygenase product) by 53% [3].in smoke-exposed rabbits, pretreatment with piriprost attenuated the smoke-induced increase in alveolar-capillary barrier permeability and decrease in plasminogen activator activity and causes a swelling of type i alveolar epithelium [4].

References

[1] bach m k, brashler j r, white g j, et al. experiments on the mode of action of piriprost (u-60,257), an inhibitor of leukotriene formation in cloned mouse mast cells and in rat basophil leukemia cells[j]. biochemical pharmacology, 1987, 36(9): 1461-1466.
[2] smith m j h, ford‐hutchinson a w, bray m a. leukotriene b: a potential mediator of inflammation[j]. journal of pharmacy and pharmacology, 1980, 32(1): 517-518.
[3] cejic s s, kennedy t g. examination of the effects of piriprost (u-60,257 b) on alkaline phosphatase activity of rat endometrial stromal cells in vitro[j]. prostaglandins, 1991, 42(2): 179-189.
[4] itten m l, grad r, quan s f, et al. piriprost pretreatment attenuates the smoke-induced increase in 99mtcdtpa lung clearance[j]. experimental lung research, 1990, 16(4): 339-353.

PIRIPROST POTASSIUM SALT Preparation Products And Raw materials

Raw materials

Preparation Products

PIRIPROST POTASSIUM SALT Suppliers

Global( 15)Suppliers
Supplier Tel Email Country ProdList Advantage
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 52927 58
Hangzhou Synstar pharmaceutical Technology CO.,Ltd 0571-85361029 synstar518@163.com China 1991 58
BOC Sciences -- info@bocsci.com USA 0 65
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8141 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 8740 58
ApexBio Technology -- sales@apexbt.com United States 6254 58

88851-62-1(PIRIPROST POTASSIUM SALT)Related Search:

[4R-[4A(1E,3S*),5B]]-1,4,5,6-TETRAHYDRO-5-HYDROXY-4-(3-HYDROXY-1-OCTENYL)-1-PHENYL-CYCLOPENTA[B]PYRROLE-2-PENTANOIC ACID, POTASSIUM SALT 1,4(R),5(R),6-TETRAHYDRO-5-HYDROXY-4-[(1E,3S)-HYDROXY-1-OCTENYL]-1-PHENYL-CYCLOPENTA[B]PYRROLE-2-PENTANOIC ACID, MONOPOTASSIUM SALT PIRIPROST POTASSIUM SALT U-60257B U60,257B POTASSIUM SALT [4r-[4α(1e,3s*),5β]]-1,4,5,6-tetrahydro-5-hydroxy-4-(3-hydroxy-1-octenyl)-1-phenyl-cyclopenta[b]pyrrole-2-pentanoic acid, potassium salt U60,257B, [4R-[4α(1E,3S*),5β]]-1,4,5,6-Tetrahydro-5-hydroxy-4-(3-hydroxy-1-octenyl)-1-phenyl-cyclopenta[b]pyrrole-2-pentanoic acid, potassium salt potassium:5-[(4R,5R)-5-hydroxy-4-[(E,3S)-3-hydroxyoct-1-enyl]-1-phenyl-5,6-dihydro-4H-cyclopenta[b]pyrrol-2-yl]pentanoate 88851-62-1 C25H32NO4K C26H34NO4K Lipoxygenase (5-) L to O Enzymes, Inhibitors, and Substrates Enzyme Inhibitors by Enzyme Enzyme Inhibitors BioChemical Biochemicals and Reagents