Cryptophycin a
Web用于防止癌细胞转移的化合物、组合物和方法专利检索,用于防止癌细胞转移的化合物、组合物和方法属于肝细胞生物学专利检索,找专利汇即可免费查询专利,肝细胞生物学专利汇是一家知识产权数据服务商,提供专利分析,专利查询,专利检索等数据服务功能。 WebCryptophycin is a class of cyclic depsipeptides that was originally isolated from the cyanobacteria Nostoc sp. (Figure 1, right) in 1990 by researchers at Merck as a potent fungicide, however, the compound was found to be highly toxic to be developed as antifungal. Some years later, crypthophycins were discovered to be potent cytotoxins.
Cryptophycin a
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WebSynthesized highly potent cryptophycin macrolides and structural analogs. Developed a creative transformation for the stereospecific epoxidation of vicinol diols in the presence … WebCryptophycin 1, produced by Nostoc sp. GSV 224, is a potent cytotoxic anti-microtubule agent. Cryptophycin 1 can induce cell apoptosis, and has anti-tumor activity and excellent anti-proliferation ability. Category ADCs Cytotoxin Product Name Cryptophycin 1 CAS 124689-65-2 Catalog Number BADC-00569 Molecular Formula C35H43ClN2O8 Molecular …
WebSep 30, 2005 · Chlorinated natural products include vancomycin and cryptophycin A. Their biosynthesis involves regioselective chlorination by flavin-dependent halogenases. We … WebKR102512597B1 KR1020247033500A KR20247033500A KR102512597B1 KR 102512597 B1 KR102512597 B1 KR 102512597B1 KR 1020247033500 A KR1020247033500 A KR 1020247033500A KR 20247033500 A KR20247033500 A KR 20247033500A KR 102512597 B1 KR102512597 B1 KR 102512597B1 Authority KR South Korea Prior art keywords cmet …
WebThe TE domain on the enzymatic assembly line converts the intermediate shown below to Cryptophycin 24. In 1-2 sentences, specify whether the TE domain catalyzes the hydrolysis or the cyclization (macrolactonization) to generate Cryptophycin 24 and explain one feature of the TE domain that will enable the desired reaction outcome. WebSep 3, 2024 · In other hand, cryptophycin-38 is a stereoisomer of cryptophycin-1 containing a S, S epoxide group in unit A. Similarly, cryptophycin-326 is an analog of cryptophycin-21 but it has two chlorines ortho to the methoxy group in unit B (Chaganty et al., 2004). Chemical structures of cryptophycin and its analogs are shown in Figure 1F. Biological ...
WebCryptophycin-38 is a stereoisomer of cryptophycin-1 (1) and to date is the only naturally occurring analogue that possesses a S,S epoxide group in unit A. Cryptophycin-327 is a geometric isomer that differs from 1 in having a cis Delta(2)-double bond in unit A. Cryptophycin-326 is related to cryptophycin-21, but has two chlorines ortho to the …
Web条件活性抗粘附分子-4(nectin-4)抗体专利检索,条件活性抗粘附分子-4(nectin-4)抗体属于抗肿瘤药专利检索,找专利汇即可免费查询专利,抗肿瘤药专利汇是一家知识产权数据服务商,提供专利分析,专利查询,专利检索等数据服务功能。 chip shop just eatWebAug 24, 2024 · Provided herein, inter alia, are PD-L1(+) natural killer cells that express soluble IL-15, PD-L1(+) natural killer cells that express soluble IL-15 and truncated EGFR, and methods of treating cancer using the PD-L1 (+) natural killer cells. In an aspect is provided a method of treating cancer in a patient in need thereof comprising administering to the … chip shop kidsgroveWebAug 4, 1998 · Cryptophycin-52 (LY355703) is a new synthetic member of the cryptophycin family of antimitotic antitumor agents that is currently undergoing clinical evaluation. At high concentrations (≥10 times the IC50), cryptophycin-52 blocked HeLa cell proliferation at mitosis by depolymerizing spindle microtubules and disrupting chromosome organization. graph calling apiWebEpoxidation provided cryptophycin-24 (arenastatin A). * To whom correspondence should be addressed. Phone: (785) 864-4498. Fax: (785) 864-5836. Supporting Information Available … graph calendar itemWebMar 10, 1997 · The cryptophycins, isolated from blue-green algae (Nostoc sp.) by Schwartz et aL and Moore and collaborators, are potent fungicides2 and antitumor agents.3,4 Among several cryptophycins isolated from the algae, cryptophycin A (1, Scheme 1) was the major cytotoxin and displayed IC50 values of 3 pg/mL against KB and 5 pg/mL against LoVo … graph call batchingWebDec 15, 2006 · The cryptophycins (e.g., cryptophycin 1; Figure 1, panel a) are among the most promising candidates for such a new drug. Like many other natural products, several of marine origin, the cryptophycins interfere with the dynamics of tubulin polymerization and depolymerization. This activity has a long history. graph callingWebCryptophycin 1 is one of the most potent tubulin-destabilizing agents ever discovered, resulting in cellular arrest at the G2/M phase via hyperphosphorylation of Bcl-2, thereby … graph calendars.readwrite