下載本文檔
版權(quán)說(shuō)明:本文檔由用戶提供并上傳,收益歸屬內(nèi)容提供方,若內(nèi)容存在侵權(quán),請(qǐng)進(jìn)行舉報(bào)或認(rèn)領(lǐng)
文檔簡(jiǎn)介
1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemEUlipristal acetateCat. No.: HY-16508CAS No.: 126784-99-4Synonyms: CDB-2914分式: CHNO分量: 475.62作靶點(diǎn): Progesterone Receptor作通路: Others儲(chǔ)存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性數(shù)據(jù)體外實(shí)驗(yàn) DMSO : 33.33 mg/mL
2、(70.08 mM; Need ultrasonic)H2O : 40% PEG300 5% Tween-80 45% salineSolubility: 2.5 mg/mL (5.26 mM); Clear solution2. 請(qǐng)依序添加每種溶劑: 10% DMSO 90% corn oilSolubility: 2.5 mg/mL (5.26 mM); Clear solution1/3 Master of Small Molecules 您邊的抑制劑師www.MedChemEBIOLOGICAL ACTIVITY物活性 Ulipristal acetate種選擇性 體酮受體調(diào)節(jié)劑 (s
3、elective progesterone receptor modulator),于治療良性婦科疾病如宮肌瘤。體外研究 Ulipristal acetate blocks activin A modulation of fibronectin and vascular endothelial growth factor A (VEGF-A) mRNA expression in cultured myometrial and leiomyoma cells 2. Ulipristal acetate decreases the DNAfragmentation at the 100-ng/m
4、L dose and continuing up to the 10,000-ng/mL dose compared to thosespermatozoa in the control group 3.體內(nèi)研究 Ulipristal and CDB-4124 have significant antiprogestational activity in vivo 1. Ulipristal acetate decreasesincidences of fibroadenomas and adenocarcinomas in the mammary gland in all treated g
5、roups. Ulipristalacetate exposure AUC(0-24h) at the highest dose in rats is 67 times human therapeutic exposure at 10mg/day. In mice, no tumor of any type increases at Ulipristal acetate exposures up to 313 times oftherapeutic exposure. Ulipristal acetate-related findings in mice are limited to orga
6、n weight changes in theliver, pituitary, thyroid/parathyroid glands, and epididymis as well as minimal panlobular hepatocellularhypertrophy in male and female mice receiving 130 mg/kg/day 4. Ulipristal acetate (1 mg/kg and 5 mg/kg)increases the frequency with which pathologists assessed the endometr
7、ium as being thickened compared tocontrols in a dose-dependent manner. There is a slight decrease in secretory differentiation with increasingdose of Ulipristal acetate, with small decreases in frequency of sub- and supra-nuclear vacuolation 5.PROTOCOLAnimal The study consisted of four groups, each
8、comprising four female cynomolgus monkeys. The groupsAdministration 5 eitherreceive ASV (control), or Ulipristal acetate at dose levels of 1, 5, or 25 mg/kg for 39 weeks. Twoadditional animals are allocated to the control and high dose groups for an 8-week post-dose recoveryperiod. At randomization,
9、 there is no statistically significant difference between treatment groups in meanbody weight. The vehicle or Ulipristal acetate is administered to all groups by oral gavage for 273consecutive days at a dose volume of 2 mL/kg. Following the dosing or recovery period, animals areeuthanized by intrave
10、nous administration of sodium pentobarbital followed by exsanguination of the femoralvessels.MCE has not independently confirmed the accuracy of these methods. They are for reference only.戶使本產(chǎn)品發(fā)表的科研獻(xiàn) Hum Reprod. 2015 Apr;30(4):800-11.See more customer validations on HYPERLINK / www.MedChemEREFERENCE
11、S1. Attardi BJ, et al. In vitro antiprogestational/antiglucocorticoid activity and progestin and glucocorticoid receptor binding of the putative2/3 Master of Small Molecules 您邊的抑制劑師www.MedChemEmetabolites and synthetic derivatives of CDB-2914, CDB-4124, and mifepristone. J Steroid Biochem Mol Biol.
12、2004 Ma2. Ciarmela P, et al. Ulipristal acetate modulates the expression and functions of activin a in leiomyoma cells. Reprod Sci. 2014Sep;21(9):1120-5.3. Munuce MJ, et al. Effects of ulipristal acetate on sperm DNA fragmentation during in vitro incubation. Eur J Contracept Reprod HealthCare. 2013
13、Oct;18(5):355-63.4. Pohl O, et al. Carcinogenicity and chronic rodent toxicity of the selective progesterone receptor modulator ulipristal acetate. Curr DrugSaf. 2013 Apr;8(2):77-97.5. Pohl O, et al. A 39-week oral toxicity study of ulipristal acetate in cynomolgus monkeys. Regul Toxicol Pharmacol. 2013 Jun;66(1):6-12.McePdf
溫馨提示
- 1. 本站所有資源如無(wú)特殊說(shuō)明,都需要本地電腦安裝OFFICE2007和PDF閱讀器。圖紙軟件為CAD,CAXA,PROE,UG,SolidWorks等.壓縮文件請(qǐng)下載最新的WinRAR軟件解壓。
- 2. 本站的文檔不包含任何第三方提供的附件圖紙等,如果需要附件,請(qǐng)聯(lián)系上傳者。文件的所有權(quán)益歸上傳用戶所有。
- 3. 本站RAR壓縮包中若帶圖紙,網(wǎng)頁(yè)內(nèi)容里面會(huì)有圖紙預(yù)覽,若沒(méi)有圖紙預(yù)覽就沒(méi)有圖紙。
- 4. 未經(jīng)權(quán)益所有人同意不得將文件中的內(nèi)容挪作商業(yè)或盈利用途。
- 5. 人人文庫(kù)網(wǎng)僅提供信息存儲(chǔ)空間,僅對(duì)用戶上傳內(nèi)容的表現(xiàn)方式做保護(hù)處理,對(duì)用戶上傳分享的文檔內(nèi)容本身不做任何修改或編輯,并不能對(duì)任何下載內(nèi)容負(fù)責(zé)。
- 6. 下載文件中如有侵權(quán)或不適當(dāng)內(nèi)容,請(qǐng)與我們聯(lián)系,我們立即糾正。
- 7. 本站不保證下載資源的準(zhǔn)確性、安全性和完整性, 同時(shí)也不承擔(dān)用戶因使用這些下載資源對(duì)自己和他人造成任何形式的傷害或損失。
最新文檔
- 廣東石油化工學(xué)院《Andoid基礎(chǔ)編程》2023-2024學(xué)年第一學(xué)期期末試卷
- 廣東汕頭幼兒師范高等??茖W(xué)?!兜谝煌鈬?guó)語(yǔ)英》2023-2024學(xué)年第一學(xué)期期末試卷
- 廣東農(nóng)工商職業(yè)技術(shù)學(xué)院《生物制藥學(xué)科前沿進(jìn)展》2023-2024學(xué)年第一學(xué)期期末試卷
- 廣東茂名幼兒師范??茖W(xué)?!洞黉N策略》2023-2024學(xué)年第一學(xué)期期末試卷
- 廣東茂名健康職業(yè)學(xué)院《英國(guó)文學(xué)下》2023-2024學(xué)年第一學(xué)期期末試卷
- 廣東理工職業(yè)學(xué)院《美國(guó)社會(huì)與文化》2023-2024學(xué)年第一學(xué)期期末試卷
- 一年級(jí)數(shù)學(xué)計(jì)算題專項(xiàng)練習(xí)集錦
- 大腦的奧秘:神經(jīng)科學(xué)導(dǎo)論(復(fù)旦大學(xué))學(xué)習(xí)通測(cè)試及答案
- 【2022屆走向高考】高三數(shù)學(xué)一輪(北師大版)基礎(chǔ)鞏固:第8章-第1節(jié)-簡(jiǎn)單幾何體及其三視圖和直觀圖
- 2022韶山市高考英語(yǔ)閱讀理解及書面表達(dá)精煉(8)及答案
- 智慧金融合同施工承諾書
- 術(shù)后甲狀旁腺功能減退癥管理專家共識(shí)
- 【7道期末】安徽省安慶市區(qū)2023-2024學(xué)年七年級(jí)上學(xué)期期末道德與法治試題(含解析)
- 2024年01月22094法理學(xué)期末試題答案
- 2024年1月國(guó)家開(kāi)放大學(xué)法律事務(wù)專科《民法學(xué)(1)》期末紙質(zhì)考試試題及答案
- 學(xué)校2024-2025學(xué)年教研工作計(jì)劃
- 安徽省蕪湖市2023-2024學(xué)年高一上學(xué)期期末考試 歷史 含解析
- 煙草執(zhí)法課件教學(xué)課件
- 2024年安全文化建設(shè)實(shí)施方案
- 康復(fù)治療技術(shù)歷年真題單選題100道及答案
- 數(shù)字化交付施工方案
評(píng)論
0/150
提交評(píng)論