硕士论文——基于光照复用的变光照三维采集系统的设计与实现.doc
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1、帀(币搀椀币币币讀缁缀済漁螏頀h砀椀嬂眃眃眃愈椈椈椈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈鄈錈爀椀琀愀渀渀椀氀愀挀琀漀渀攀愀琀愀匀栀攀攀琀攀搀栀攀洀砀瀀爀攀猀猀瀀搀昀瀀椀挀最椀昀爀椀琀愀渀渀椀氀愀挀琀漀渀攀愀琀愀匀栀攀攀琀攀搀栀攀洀砀瀀爀攀猀猀瀀搀昀尀尀攀攀攀攀戀搀搀搀戀搀攀挀攀戀娀礀戀搀洀伀攀氀愀眀瀀栀洀琀礀瀀礀甀爀洀渀儀砀砀戀氀攀渀欀刀愀爀漀爀瘀吀刀挀娀爀椀琀愀渀渀椀氀愀挀琀漀渀攀愀琀愀匀栀攀攀琀攀搀栀攀洀砀瀀爀攀猀猀愀愀搀戀搀愀戀戀挀搀爀椀琀愀渀渀椀氀愀挀琀漀渀攀愀琀一漀夀一匀一漀漀氀攀挀甀氀愀爀漀爀洀甀氀愀脀蔠舀舠传萀漀氀攀挀甀氀愀爀圀攀椀最栀琀吀愀爀最攀琀伀琀栀攀爀猀倀愀琀栀眀愀礀伀琀栀
2、攀爀猀匀琀漀爀愀最攀倀氀攀愀猀攀猀琀漀爀攀琀栀攀瀀爀漀搀甀挀琀甀渀搀攀爀琀栀攀爀攀挀漀洀洀攀渀搀攀搀挀漀渀搀椀琀椀漀渀猀椀渀琀栀攀伀匀漀氀瘀攀渀琀愀甀琀椀漀渀倀爀漀搀甀挀琀栀愀猀渀漀琀戀攀攀渀昀甀氀氀礀瘀愀氀椀搀愀琀攀搀昀漀爀洀攀搀椀挀愀氀愀瀀瀀氀椀挀愀琀椀漀渀猀漀爀爀攀猀攀愀爀挀栀甀猀攀漀渀氀礀吀攀氀愀砀洀愀椀氀琀攀挀栀攀搀栀攀洀砀瀀爀攀猀猀挀漀洀搀搀爀攀猀猀攀攀爀倀愀爀欀爀匀甀椀琀攀儀漀渀洀漀甀琀栀甀渀挀琀椀漀渀一唀匀倀爀漀搀甀挀琀愀琀愀匀栀攀攀琀渀栀椀戀椀琀漀爀猀最漀渀椀猀琀猀匠挀爀攀攀渀椀渀最椀戀爀愀爀椀攀猀眀眀眀攀搀栀攀洀砀瀀爀攀猀猀挀漀洀攀搀栀攀洀砀瀀爀攀猀猀渀7币礎:e胔-輀%棙
3、i缀笝$BRL44385-DataSheet-MedChemExpress.pdfpic1.gifBRL44385DataSheetMedChemExpress.pdf2019-531946bd55a-fd25-42c4-ab37-864a50518f16vW9gi9OIwkL92ZYE5wVgl0LzhKtoXiZDKyiY0Qd314I2pguhayYB6A=BRL44385,DataSheet,MedChemExpress83fe3f24b2babd562a14fbe0b0e37185BRL44385Cat. No.: HY-U00224CAS No.: 114778-60-8Molec
4、ular Formula: CHNOMolecular Weight: 225.2Target: HSVPathway: Anti-infectionStorage: Please store the product under the recommended conditions in the COA.Solvent HSV-2In Vivo BRL44385 is a selective antiherpesvirus agent. Following oral administration, BRL 55792 is very well absorbed and provides hig
5、h and prolonged concentrations of BRL44385 in the blood. In mice 15 min and 60 min after administration of a single oral dose of BRL 55792, the concentrations of BRL44385 in the blood are considerably higher than those obtain after oral administration of either BRL44385 or BRL46720 and the bioavaila
6、bility of BRL 44385 from oral BRL 55792 is 66% of that achieves with the same dose of the sodium salt of BRL44385 administered intravenously1.PROTOCOLProduct Data Sheet InhibitorsAgonistsScreening Librarieswww.MedChemE1Animal Administration 1Mice1 BRL44385 is administered as a single dose of 0.2 mmo
7、l/kg in 0.1 mL of 1% carboxymethylcellulose by oral gavage to female Balb/c mice weighing approximately 20 g. Food is withheld for 18 h prior to the start of the experiment. Blood is collected by cardiac puncture using heparinized syringes 15, 60, and 180 min after dosing. Equal volumes (0.2 mL) fro
8、m three mice are pooled at each time point and 0.6 mL of 16% trichloroacetic acid is added. After centrifugation, 0.5 mL of supernatant is added to 0.1 mL of saturated aqueous NaHCO3 followed by the addition of 0.6 mL of 0.4 mM NH4OAc (pH 6.0) and the mixture analysed by HPLC. MCE has not independen
9、tly confirmed the accuracy of these methods. They are for reference only.REFERENCES1. M. R. Harnden, et al. Synthesis, oral bioavailability and in vivo activity of acetal derivatives of the selective antiherpesvirus agent 9-(3-hydroxypropoxy) guanine (SRL 44385). Antiviral Chemistry & Chemotherapy (
10、1994) 5(3), 147-154.Caution: Product has not been fully validated for medical applications. For research use only.Tel: 609-228-6898 Fax: 609-228-5909 E-mail: techMedChemEAddress: 1 Deer Park Dr, Suite Q, Monmouth Junction, NJ 08852, USAwww.MedChemE2MedChemExpress0001200001可研报告20190531134349545965B砀(
11、币匀攀币氂币币讀缁缀渌漁螏頀h砀椀蜂匂圄弄弄弄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄蜄褄礀搀爀漀砀礀瀀爀漀瀀礀氀戀攀琀愀挀礀挀氀漀搀攀砀琀爀椀渀匀匀攀搀栀攀洀砀瀀爀攀猀猀瀀搀昀瀀椀挀最椀昀礀搀爀漀砀礀瀀爀漀瀀礀氀戀攀琀愀挀礀挀氀漀搀攀砀琀爀椀渀匀匀攀搀栀攀洀砀瀀爀攀猀猀瀀搀昀尀尀愀搀愀攀戀昀挀戀戀戀攀愀昀愀挀挀倀戀堀伀琀圀栀唀礀漀甀堀砀猀椀爀戀氀漀栀倀砀渀戀娀夀伀挀猀樀儀戀眀礀搀爀漀砀礀瀀爀漀瀀礀氀戀攀琀愀挀礀挀氀漀搀攀砀琀爀椀渀匀匀攀搀栀攀洀砀瀀爀攀猀猀昀戀昀挀戀攀戀攀昀挀攀栀堀L攀搀栀攀洀砀瀀爀攀猀猀靓言茀渀7币沃:e區胔-輀8棙i缀$3-Methylthio-propionic-acid-D
12、ataSheet-MedChemExpress.pdfpic1.gif3MethylthiopropionicacidDataSheetMedChemExpress.pdf2019-5312645dace-8962-41af-9cce-b3c026111f0bKlL0ABKV7xLQvwdqaumrMQj1j0zCJ6gv3JN1OltKeMiv6QKAqqObSw=Methylthio,propionic,acid,DataSheet,MedChemExpress9d66e7b8f471fff3d8e2e78bfaf5289b3-(Methylthio)propionic acidCat.
13、No.: HY-101401CAS No.: 646-01-5Molecular Formula: CHOSMolecular Weight: 120.17Target: FungalPathway: Anti-infectionStorage: Pure form -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 monthSolvent 253(21):7844-50.2. Surette R, et al. Formation of 3-methylthioacrylic acid from methionine by Strept
14、omyces lincolnensis. Isolation of a peroxidase. J Antibiot (Tokyo). 1976 Jun;29(6):646-52.3. Kim YC, et al. 3-methylthiopropanoic acid produced by Enterobacter intermedium 60-2G inhibits fungal growth and weed seedling development. J Antibiot (Tokyo). 2003 Feb;56(2):177-80.4. Nakamura Y, et al. 3-Me
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