Bimatoprost CAS#155206-00-1
Bimatoprost , Promotion Season Now in Store and Free Sample for Testing with Factory Price
Chemical Name: Bimatoprost
CAS No.:155206-00-1
Molecular FormulaC25H37NO4
Average mass566
Appearance: White to off white crystalline powder
Sample: Available

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Description of Bimatoprost
Bimatoprost (marketed in the US, Canada and Europe by Allergan, under the trade name Lumigan) is a prostaglandin analog used topically (as eye drops) to control the progression of glaucoma and in the management of ocular hypertension. It reduces intraocular pressure (IOP) by increasing the outflow of aqueous fluid from the eyes. In December 2008, the indication to lengthen eyelashes was approved by the U.S. Food and Drug Administration (FDA); the cosmetic formulation of bimatoprost is sold as Latisse .
Basic Info of Bimatoprost
Chemical Name | bimatoprost |
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Synonyms | BiMatoprost HOUSE STANDARD;BiMapnost;Prostamide;17-Phenyl-tri-norprostaglandin F2α-ethyl amide;LUMIGAN;Expand |
CAS No. | 155206-00-1 |
Molecular Formula | C25H37NO4 |
Molecular Weight | 415.56600 |
PSA | 89.79000 |
LogP | 3.53780 |
Safety Info
WGK Germany | 3 |
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Properties
Appearance & Physical State | crystalline solid |
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Density | 1.145 g/cm3 |
Boiling Point | 629.8ºC at 760 mmHg |
Flash Point | 334.7ºC |
Refractive Index | 1.591 |
Storage Condition | -20ºC |
Vapor Pressure | 9.94E-17mmHg at 25°C |
Numbering system
MDL number | MFCD03411999 |
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What is Bimatoprost?
With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is Ambroxan which has developed particularly rapidly in recent years. Do you know about Ambroxan?
The official answer: Bimatoprost, molecular formula is C25H37NO4, molecular weight is 415.5656
What’s the application of Bimatoprost?
Olaparib is a PARP inhibitor that also acts on BRCA1 or BRCA2 mutations. olaparib has little effect on end-anchor (polymerase)-1 with an IC50 value greater than. olaparib concentrations of 30-100 nM act on SW620 cells to inactivate PARP-1. Compared to BRCA1 and BRCA2 adequate cell lines (Hs578T,MDA-MB-23Chemicalbook1,T47D), BRCA1-deficient cell lines (MDA-MB-463[1] and HCC1937) were overly sensitive to Olaparib Olaparib inhibited PARP and blocked base excision repair, resulting in KB2P cells to be strongly sensitive to Olaparib. The result leads to a shift from single-strand breaks to double-strand breaks during DNA replication and consequent activation of the BRCA2-dependent recombination pathway.
Conclusion
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