ライフサイエンスコーパス: maytansinoid

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1 tigen-specific fashion upon conjugation with maytansinoid.

2 that is specific for PSMA conjugated to drug maytansinoid 1 (DM1), a microtubule-depolymerizing compo

3 the maytansinoid antimicrotubule agent drug maytansinoid-1 directly to prostate-specific membrane an

4 gnificance, we report that a clinically used maytansinoid ADC, ado-trastuzumab emtansine (T-DM1), wit

5 ing, the therapeutic activity of trastuzumab maytansinoid ADCs can be further improved.

6 lusters required for the biosynthesis of the maytansinoid, ansamitocin, from a cosmid library of Acti

7 ument in favor of IMGN529, a novel anti-CD37 maytansinoid antibody-drug conjugate (ADC), elegantly sh

8 uses trastuzumab to specifically deliver the maytansinoid antimicrotubule agent DM1 to HER2-positive

9 s an immunoconjugate designed to deliver the maytansinoid antimicrotubule agent drug maytansinoid-1 d

10 Maytansinoids are potent antitumor agents found in plant

11 in and conjugates of potent tubulin poisons (maytansinoids auristatins and taxoids) are undergoing cl

12 A series of new maytansinoids, bearing a disulfide or thiol substituent

13 Our results strongly suggest that maytansinoid-conjugated anti-PSCA monoclonal antibodies

14 Maytansinoid-conjugated antibodies caused complete regre

15 amined the metabolic fate in cells of huC242-maytansinoid conjugates containing either a disulfide li

16 ght into the mechanism of action of antibody-maytansinoid conjugates in general, and more specificall

17 Antiproliferative effects of trastuzumab-maytansinoid conjugates were evaluated on cultured norma

18 ing is required for the activity of antibody-maytansinoid conjugates, irrespective of the linker.

19 s to better define this process for antibody-maytansinoid conjugates.

20 for the characterization of other ADCs with maytansinoid derivatives as payload.

21 vitro and in vivo antitumor activity of the maytansinoid DM1 (N(2')-deacetyl-N(2')-(3-mercapto-1-oxo

22 sistance, we conjugated the highly cytotoxic maytansinoid DM1 to antibodies via the maleimidyl-based

23 A) to a potent microtubule-inhibiting agent, maytansinoid DM1, via an intramolecular disulfide bond.

24 The antibody was conjugated to the maytansinoid, DM1, a potent antimicrotubule agent, via t

25 tor 2 (HER2) antibody, trastuzumab, with the maytansinoid, DM1, a potent microtubule-disrupting agent

26 al antibody linked to the tubulin-disrupting maytansinoid DM4, in a population of patients with FRalp

27 In contrast, therapy with the free maytansinoid drug (in the form of DM1-S-Me) proved not t

28 o yield metabolites consisting of the intact maytansinoid drug and linker attached to lysine.

29 ugates between monoclonal antibodies and the maytansinoid drug DM1 (MAb-DM1).

30 The maytansinoid drug DM1 is 100- to 1000-fold more cytotoxi

31 ped for detection and quantification of free maytansinoid drug in disulfide-linked conjugates between

32 ses of potent anti-tubulins, auristatins and maytansinoids, indiscriminately radiosensitize tumour ce

33 (epsilon)-SMCC-DM1 as the sole intracellular maytansinoid metabolite.

34 harmacokinetics, and toxicity of trastuzumab-maytansinoid (microtubule-depolymerizing agents) conjuga

35 so identified and characterized the released maytansinoid molecules from these conjugates, and measur

36 HuN901 conjugated with the maytansinoid N(2')-deacetyl-N(2')-(3-mercapto-1-oxopropy

37 h the microtubule-formation inhibitor DM1 (a maytansinoid), or with the DNA alkylator DC1 (a CC1065 a

38 d trastuzumab or trastuzumab linked to other maytansinoids through disulfide linkers.

39 The targeted delivery of these maytansinoids, using monoclonal antibodies, resulted in

40 Several of these maytansinoids were found to be even more potent in vitro

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