Antitumor agent-127

Antitumor Agent-127 is a designed peptide-like molecule with functional groups tuned for binding to structured protein pockets. Hydrophobic and aromatic residues contribute to strong contact interfaces, while polar residues regulate solubility. Researchers assess its conformational behavior and bio-target interactions. Applications include ligand-discovery studies, structural-activity mapping, and mechanistic evaluation.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: R2877

Synonyms/Alias:Antitumor agent-127; CHEMBL5416192; BDBM50625770; HY-161096; CS-0926573

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M.F/Formula
C86H107N15O18S
M.W/Mr.
1670.9
Sequence
One Letter Code:FYLVYSGWYFLXG
Three Letter Code:Ac(1)-Phe-Tyr-Leu-Val-Tyr-Ser-Gly-Trp-Tyr-N(Me)Phe-Leu-Cys(1)-Gly-NH2

Antitumor agent-127 is a small-molecule research compound recognized for its activity in modulating cellular proliferation pathways associated with tumorigenesis. As a synthetic chemical entity, it has garnered interest in the biochemical research community due to its capacity to interfere with mechanisms central to cancer cell growth and survival. Its molecular design is tailored to engage specific targets implicated in oncogenic signaling, making it a valuable tool for investigating the molecular underpinnings of tumor biology. The compound's functional significance lies in its potential to elucidate the dynamics of cell cycle regulation, apoptosis, and other processes pivotal to malignant transformation and progression.

Target validation: Antitumor agent-127 is widely utilized in target validation studies to confirm the functional relevance of candidate proteins or pathways involved in cancer. By selectively inhibiting or modulating specific molecular targets, researchers can assess the downstream effects on cell proliferation, survival, and signal transduction. This approach aids in distinguishing between driver and passenger alterations in tumorigenesis, thereby refining the selection of actionable molecular targets for further investigation.

Mechanistic studies: The compound provides a robust platform for dissecting the biochemical mechanisms underlying tumor cell responses to pathway inhibition. Through its application in in vitro and cell-based assays, scientists can monitor changes in phosphorylation states, transcriptional activity, and protein-protein interactions. Such mechanistic insights are critical for understanding resistance phenomena, feedback regulation, and compensatory signaling networks that often complicate therapeutic strategies.

High-throughput screening: Antitumor agent-127 serves as a reference molecule or positive control in high-throughput screening assays designed to identify novel compounds with antitumor potential. Its well-characterized activity profile enables the benchmarking of assay performance and facilitates the differentiation of true hits from background noise. This application is particularly valuable in drug discovery pipelines, where large chemical libraries are interrogated for modulators of oncogenic pathways.

Cellular pathway analysis: Researchers employ this compound to probe the integrity and modulation of key signaling cascades such as PI3K/AKT, MAPK/ERK, or other relevant oncogenic pathways. By assessing the impact of the agent on pathway activity, investigators can delineate the interdependencies and crosstalk that govern tumor cell fate decisions. Such analyses contribute to a deeper understanding of network vulnerabilities that may be exploited for combinatorial intervention strategies.

Resistance mechanism exploration: The use of Antitumor agent-127 in resistance mechanism studies enables the identification of adaptive responses and secondary mutations that confer insensitivity to pathway inhibition. By exposing tumor cell models to the compound under varying conditions, researchers can map the molecular changes associated with acquired resistance. These findings inform the design of next-generation inhibitors and combination regimens aimed at overcoming or circumventing resistance barriers in cancer research models.

InChI
InChI=1S/C86H107N15O18S/c1-48(2)34-62-78(111)99-70(77(110)89-43-72(87)106)46-120-47-74(108)92-64(36-51-16-10-8-11-17-51)79(112)94-65(37-53-22-28-57(103)29-23-53)80(113)93-63(35-49(3)4)83(116)100-75(50(5)6)85(118)96-66(38-54-24-30-58(104)31-25-54)81(114)98-69(45-102)76(109)90-44-73(107)91-67(41-56-42-88-61-21-15-14-20-60(56)61)82(115)97-68(39-55-26-32-59(105)33-27-55)86(119)101(7)71(84(117)95-62)40-52-18-12-9-13-19-52/h8-33,42,48-50,62-71,75,88,102-105H,34-41,43-47H2,1-7H3,(H2,87,106)(H,89,110)(H,90,109)(H,91,107)(H,92,108)(H,93,113)(H,94,112)(H,95,117)(H,96,118)(H,97,115)(H,98,114)(H,99,111)(H,100,116)/t62-,63-,64-,65-,66-,67-,68-,69-,70-,71-,75-/m0/s1
InChI Key
ILLCRYUBFFYODW-IMSYTBADSA-N

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