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Results for "

e-101

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    14
    TargetMol | All_Pathways
  • Inhibitory Antibodies
    1
    TargetMol | Inhibitory_Antibodies
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    4
    TargetMol | All_Dye_Reagents
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    TargetMol | PROTAC
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    TargetMol | Natural_Products
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    TargetMol | Recombinant_Protein
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Riboflavin
Vitamin B2, E101
T093783-88-5
Riboflavin (Vitamin B2) is a natural product, an endogenous human metabolite, and a micronutrient. Riboflavin is essential for the formation of two major coenzymes, flavin mononucleotide and flavin adenine dinucleotide. Riboflavin is involved in energy metabolism, cellular respiration, and antibody production, as well as normal growth and development.
  • $33
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TargetMol | Citations Cited
Bunazosin Hydrochloride
E-643, E643, E-1015, E 643, E 1015
T2692352712-76-2In house
Bunazosin Hydrochloride (E 1015) is an alpha(1)-adrenoceptor antagonist used as a systemic antihypertensive and an ocular hypotensive drug.
  • $34
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SWE101
T130422376322-12-0
SWE101 is a potent human and rat soluble epoxide hydrolase (sEH)-P inhibitor(IC50s of 4 μM and 2.8 μM, respectively).
  • $284
6-8 weeks
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E3 Ligase Ligand-linker Conjugate 101
T208949
E3LigaseLigand-linker Conjugate 101 is a conjugate consisting of an E3 ligase ligand and a linker, specifically made up of (S,R,S)-AHPC and a corresponding linker. (S,R,S)-AHPC is a von Hippel-Lindau (VHL) ligand based on VH032, capable of recruiting VHL protein. This conjugate is a crucial intermediate for synthesizing complete PROTACs molecules.
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Zeleciment basivarsen
DYNE-101
T2125652767191-74-0
Zeleciment basivarsen (DYNE-101) is an antibody oligonucleotide conjugate (AOC), consisting of a Fab antibody named Zeleciment that binds to the transferrin receptor 1 (TfR1) on muscle cells, and an antisense oligonucleotide known as Basivarsen. This compound targets the RNA of the mutant dystrophia myotonica-protein kinase (DMPK) for RNase H-mediated degradation, and is utilized in the study of myotonic dystrophy type 1 (DM1).
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FE101120
T212983
FE101120 is a non-peptidic CCK2 receptor agonist. It is utilized in diabetes research.
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5H-Dibenz[b,f]azepine-10,11-dione
T64469
5H-Dibenz[b,f]azepine-10,11-dione is a useful organic compound for research related to life sciences and the catalog number is T64469.
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    Sulforhodamine 101 DHPE
    T85159187099-99-6
    Sulforhodamine 101 DHPE, a fluorescent probe, results from the conjugation of sulforhodamine 101, a red fluorescent dye with excitation/emission spectra of 586/605 nm, to the phospholipid 1,2-dipalmitoyl-sn-glycero-3-PE. It effectively integrates into phospholipid bilayers and is utilized for imaging solid supported lipid bilayers, detecting protein-ligand interactions on bilayers, and monitoring lipid probe colocalization in liposomes through resonance energy transfer (RET).
    • $449
    35 days
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    (E,E)-10,12-Hexadecadienal
    TN795469977-24-8
    (E,E)-10,12-Hexadecadienal, isolated as a female pheromone from Earias insulana, is a chemical compound.
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    (E,E)-10,12-Hexadecadienol
    TN7966765-19-5
    (E,E)-10,12-Hexadecadienol, identified as a female pheromone, has been isolated from the legume pod borer.
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    (Z,E)-10,12-Hexadecadienal
    TN797169977-23-7
    (Z,E)-10,12-Hexadecadienal functions as a pheromone in Conogethes pluto and serves as an attractant.
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    (E,E,E,)-10,12,14-Hexadecatrienal
    TN7995123363-47-3
    (E,E,E,)-10,12,14-Hexadecatrienal, a pheromone emitted by female Manduca sexta, is a chemical compound.
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    Entrectinib
    RXDX-101, NMS-E628
    T36781108743-60-7
    Entrectinib (RXDX-101) is a Trk, ROS1, and ALK inhibitor that inhibits TrkA, TrkB, TrkC, ROS1, and ALK (IC50=1/3/5/12/7 nM) with oral activity and blood-brain-barrier penetration. Entrectinib exhibits both antitumor and CNS activity.
    • $35
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    TargetMol | Citations Cited
    Zilovertamab vedotin
    VLS-101, MK-2140
    T77186
    Zilovertamab vedotin is a novel antibody-drug conjugate (ADC) constructed by conjugating the humanized monoclonal antibody zilovertamab with the anti-microtubule cytotoxic drug monomethyl vedotin. It binds to ROR1 on the surface of tumor cells, promotes rapid internalization and trafficking of the complex to lysosomes, followed by ADC cleavage and release of monomethyl vedotin, thereby inducing tumor cell apoptosis. It can be used in cancer-related research.
    • $758
    2-4 weeks
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