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Results for "

T8003

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    11
    TargetMol | All_Pathways
  • Peptide Products
    9
    TargetMol | Peptide_Products
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    1
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Methotrexate disodium
T80037413-34-5
Methotrexate disodium is an tetrahydrofolate dehydrogenase inhibitor
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Oxyntomodulin (bovine, porcine) (TFA)
Glucagon-37 (bovine, porcine) (TFA)
T80030
Oxyntomodulin (bovine, porcine) TFA is a 37-amino acid peptide hormone that functions as a glucagon-like peptide 1 (GLP-1) receptor agonist [1].
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[D-Pro2] Spantide I TFA
T80031
[D-Pro2] Spantide I TFA is an analog of Spantide I, serving as a selective antagonist of the NK1 receptor [1].
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FITC-α-Bungarotoxin
T80032
FITC-α-Bungarotoxin is the FITC-labeled form of α-Bungarotoxin, which acts as a competitive antagonist at nicotinic acetylcholine receptors (nAChRs) [1].
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Biotin-α-Bungarotoxin
T80033
Biotin-α-Bungarotoxin is a biotinylated form of α-Bungarotoxin, which acts as a competitive antagonist at nicotinic acetylcholine receptors (nAChRs) [1].
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Margatoxin TFA
T80034
Margatoxin TFA, an alpha-KTx scorpion toxin isolated from Centruroides margaritatus venom, is a 39-amino-acid peptide that serves as a high-affinity inhibitor of Kv1.3 (Kd = 11.7 pM). It also inhibits Kv1.2 (Kd = 6.4 pM) and Kv1.1 (Kd = 4.2 nM), making it a valuable tool for ion channel research [1] [2].
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Biotin-β-Amyloid (1-42), human TFA
Biotin-amyloid β-peptide (1-42) (human) TFA
T80035
Biotin-β-Amyloid (1-42), human TFA, also known as Biotin-Amyloid β-Peptide (1-42) (human) TFA, is a biotin-labeled 42-amino acid peptide implicated in the pathogenesis of Alzheimer's disease.
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TargetMol | Citations Cited
AmmTX3 TFA
T80036
AmmTX3 TFA, a peptide toxin derived from Androctonus mauretanicus scorpion venom, functions as a selective blocker of the K_v4 channel. It inhibits the A-type K^+ current with an inhibition constant (K_i) of 131 nM [1] [2].
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Bim BH3
T80038505070-06-4
Bim BH3 is a bioactive peptide that belongs to the pro-apoptotic Bcl-2 family of proteins.
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ATX-II
T8003960748-45-0
ATX-II, an Na+ channel modulator toxin derived from the sea anemone (Anemonia sulcata), causes delayed inactivation of the Na+ channels and has been linked to pulmonary vein arrhythmogenesis and atrial fibrillation [1] [2]. It exhibits interaction with halothane, caffeine, and ryanodine.
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Methotrexate-D3 diammonium
TMID-0469
Methotrexate-D3 diammonium is the deuterated form of Methotrexate diammonium (T8003). Methotrexate (Amethopterin) functions as an antimetabolite and antifolate by inhibiting dihydrofolate reductase, which prevents the conversion of folic acid to tetrahydrofolate, thereby inhibiting DNA synthesis. It also acts as an immunosuppressant and antineoplastic agent, used in treating rheumatoid arthritis and in researching various cancers, such as acute lymphoblastic leukemia.
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