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trc标准品

简要描述:TRC是加拿大全资公司,的有机化学品(包括碳水化学、芳香化学、氮磷硫化学、放射性同位素及同位素标记物等)制造商,建立于1982年,占地55,000平方英尺,包括研究实验室和生产车间,主要用于生物学、医学、药学、临床诊断和试验方面的研究和生产。TRC提供生化研究的有机化学品,用于生物技术,制药,诊断。研究特殊化学品。提供从g级到kg级别的定制合同。

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  • 更新时间:2016-05-05
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详情介绍

trc标准品  太阳集团城网站2003不仅是挪威Chiron标准品公司和意大利Chromogenix试剂公司的中国大陆代理商,还同时销售EP(欧洲药典)、USP(美国药典)、BP(英国药典)、(WHO)世界卫生组织药物标准品、英国*实验室LGC(中国区总代理)医药杂质标准品、加拿大TRC标准品(中国区代理),美国中草药ChomaDax标准品(中国授权代理商),NIST(美国国家标准局标准品)、irrm(欧洲标准局标准品)、瑞士巴亨公司(BaChem),美国Accustandard标准品,美国ChemService标准品,德国Dr.Ehrenstorfer标准品,美国剑桥CIL(同位素标准品),金属分析标准品、环境监测标准品、ICP标准品等各种产品。种类齐全,到货迅速

更多详细信息欢迎您.凡购买公司产品既可成为我公司会员,以后采购均享受“八折”优惠,如有需要,可!

公司合作伙伴:中科院化学研究所,清华大学,南开大学,燕山大学,第三军医大学,山东鲁南制药,深圳海王药业,修正集团,康师傅集团等

郑重承诺:凡是购买公司产品,出现质量问题,无条件退货退款。

trc标准品 其他相关试剂:                                                                                               
A105000 ABACAVIR SULFATE
(1S,4R)-4-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol Sulfate;
Ziagen;
C28H38N12O6S
A nucleoside reverse transcriptase inhibitor (NRTI).
Daluge, S.M., et al.: Antimicrob. Ag. Chemother., 41, 1082 (1997), Foster, R.H., et al.: Drugs, 55, 729 (1998), Staszewski, S., et al.: J. Am. Med. Assoc.,
285, 1155 (2001),
670.74 5 mg
188062-50-2
222-225°C
50 mg $
m.p.,
CAS#
m.w.,
A105002 ABACAVIR-D4
(1S,4R)-4-[2-Amino-6-[(cyclopropyl-d4)amino]-9H-purin-9-yl]-2-cyclopentene-1-methanol;
Ziagen-d4;
C14H14D4N6O
A labelled nucleoside reverse transcript

ase inhibitor (NRTI).
Daluge, S.M., et al.: Antimicrob. Ag. Chemother., 41, 1082 (1997), Foster, R.H., et al.: Drugs, 55, 729 (1998), Staszewski, S., et al.: J. Am. Med. Assoc.,
285, 1155 (2001),
290.36 222-225°C 1 mg
10 mg
m.w., m.p.,
A105010 ABACAVIR 5’- -D-GLUCURONIDE
[(1S,4R)-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopenten-1-yl]methyl- -D-Gluco
pyranosiduronic Acid; Abacavir 5’-Glucuronide;
C20H26N6O7
A metabolite of Abacavir.
Hoemans, R., et al.: Pharm. World Sci., 19, 159 (1997), Beach, J., et al.: Clin. Ther., 20, 2 (1998), McDowell, J., et al.: Antimicrob. Agents
Chemother., 43, 2855 (1999),
462.46 1 mg
384329-76-4
>211°C (dec.)
10 mg
CAS#
m.w.,
A105030 ABACAVIR 5’-(2,3,4-TRI-O-ISOBYTYRYL)- -D-GLUCURONIC ACID METHYL
ESTER
C33H46N6O10
An intermediate in the preparation of Abacavir metabolites
686.75 1 mg
10 mg
A107000 ABAMECTIN
AVERMECTIN B1; MK-936; AGRI-MEK; AVID; ZEPHYR;
C48H72O14
Mixture of avermectins, containing at least 80 of avermectin B1a (C48H72O14) and not more than 20 of avermectin B1b (C47H70O14). Used as acaricide,
insecticide.
Wang, S., et al.: Prog. Clin. Biol. Res., 97, 373 (1982), Greenblatt, J.A., et al.: J. Agric. Entomol., 3, 233 (1986), Drexler, G., et al.: Eur. J. Pharmacol.,
99, 269 (1984),
873.08 10 mg
71751-41-2
150-1550C
100 mg
m.p.,
CAS#
m.w.

A108500 ABIRATERONE ACETATE
(3β)-17-(3-Pyridinyl)androsta-5,16-dien-3-ol Acetate (Ester); CB 7630;
C26H33NO2
A novel steroidal inhibitor of human Cytochrome P450(17 -Hydroxylase-C17,20-lyase): potential agent for the treatment of prostatic cancer.
Denis, L., et al.: Cancer, 72, 3888 (1993), Potter, G.A., et al.: J. Med. Chem., 38, 2463 (1995), Denmeade, S., et al.: Nat. Rev., 2, 389
(2002), Scher, H., et al.: J. Clin. Oncol., 23, 8253 (2005),
391.55 5 mg
154229-18-2
127-130°C
50 mg
CAS#
m.w.,
A108502 ABIRATERONE ACETATE-D4
(3β)-17-(3-Pyridinyl)androsta-5,16-dien-3-ol Acetate-d4 (Ester); CB 7630-d4;
C26H29D4NO2
A novel steroidal inhibitor of human Cytochrome P450(17 -Hydroxylase-C17,20-lyase): potential agent for the treatment of prostatic cancer.
Denis, L., et al.: Cancer, 72, 3888 (1993), Potter, G.A., et al.: J. Med. Chem., 38, 2463 (1995), Denmeade, S., et al.: Nat. Rev., 2, 389
(2002), Scher, H., et al.: J. Clin. Oncol., 23, 8253 (2005),
m.w., 395.57 133-135°C 10 mg
A110000 (+)-CIS,TRANS-ABSCISIC ACID, 98
(S-(Z,E)])-5-(1-Hydroxy-2,6,6-trimethyl)-4-oxo-2-cyclohexen-1-yl-3-methyl-2,4-pentadienoic
Acid; S-ABA; Dormin;
C15H20O4
The natural isomer of the abscission-accelerating plant hormone.
Krochko, J.E., et al.: Plant Physiol., 118, 849 (1998), Jacobsen, J.V., et al.: Psysiol. Plant., 115, 428 (2002),
264.32 10 mg
21293-29-8
161-163C
100 mg
m.p.,
CAS#
m.w.,
A110002 (+)CIS,TRANS-ABSCISIC ACID-D6
[S-(Z,E)]-5-[1-Hydroxy-6,6-dimethyl-2-(methyl-d6)-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pent
adienoic Acid; S-ABA-d6; Dormin-d6;
C15H14D6O4
The natural isomer of the abscission-accelerating plant hormone.
Krochko, J.E., et al.: Plant Physiol., 118, 849 (1998), Jacobsen, J.V., et al.: Psysiol. Plant., 115, 428 (2002),
270.35 161-163°C 1 mg
10 mg
m.p.,
CAS#
m.w.,
A112500 ABT 263
4-[4-[[2-(4-Chlorophenyl)-5,5-dimethyl-1-cyclohexen-1-yl]methyl]-1-piperazinyl]-N-[[4-[[(1R)-3-(
4-morpholinyl)-1-[(phenylthio)methyl]propyl]amino]-3-[(trifluoromethyl)sulfonyl]phenyl]sulfonyl]
benzamide;
C47H55ClF3N5O6S3
A novel inhibitor of antiapoptotic BCL-2 proteins; a new promising anticancer drug candidate.
Adams, J., et al.: Science, 281, 1322 (1998), Degterev, A., et al.: Nat. Cell. Biol., 3, 173 (2001), Kitada, S., et al.: J. Med. Chem., 46, 4259 (2003),
Danial, N., et al.: Clin. Cancer Res., 13, 7254 (2007),
974.61 5 mg
923564-51-6
114-116°C
50 mg
CAS#
m.w.,
Toronto Research Chemicals Inc., 416-665-9696
2 Brisbane Rd., 416-665-4439
North York, ON, :torresch@interlog.com
Canada, M3J 2J8 URL: www.trc-canada.com
Toronto Research Chemicals Inc.
A112502 ABT 263-D8
4-[4-[[2-(4-Chlorophenyl)-5,5-dimethyl-1-cyclohexen-1-yl]methyl]-1-piperazinyl]-N-[[4-[[(1R)-3-(
4-morpholinyl)-1-[(phenylthio)methyl]propyl]amino]-3-[(trifluoromethyl)sulfonyl]phenyl]sulfonyl]
benzamide-d8;
C47H47D8ClF3N5O6S3
A novel inhibitor of antiapoptotic BCL-2 proteins; a new promising anticancer drug candidate.
Adams, J., et al.: Science, 281, 1322 (1998), Degterev, A., et al.: Nat. Cell. Biol., 3, 173 (2001), Kitada, S., et al.: J. Med. Chem., 46, 4259 (2003),
Danial, N., et al.: Clin. Cancer Res., 13, 7254 (2007),
982.66 102-107°C 1 mg
10 mg
A112550 ABT 737
4-[4-[(4’-Chloro[1,1’-biphenyl]-2-yl)methyl]-1-piperazinyl]-N-[[4-[[(1R)-3-(dimethylamino)-1-[(ph
enylthio)methyl]propyl]amino]-3-nitrophenyl]sulfonyl]benzamide;
C42H45ClN6O5S2
A selective inhibitor of BCL-2, in small cell lung cancer. ABT-737 induced dramatic regressions in tumors derived from some SCLC cell lines.
Ikegaki, N., et al.: Cancer Res., 54, 6 (1994), Kaiser, U., et al.: Lung Cancer, 15, 31 (1996), Rudin, C., et al.: J. Clin. Oncol., 22, 1110 ( 2004),
Konopleva, M., et al.: Cancer Cell, 10, 375 (2006), Trudel, S., et al.: Clin. Cancer Res., 13, 621 (2007),
813.43 2.5 mg
852808-04-9
152-154°C
25 mg
CAS#
m.w.,
 



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