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(41-90)ۣɽǢ̸
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Ʒ86101
ι۴3804579
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TN1774IsobavachromeneStreptococcus,Bacterial,Isobavachromene,mutans,Antibacterial,Inhibitor,inhibit
Isobavachromene is an inhibitor of NADH-Ubiquinone oxidoreductase and ornithine decarboxylase. Isobavachromene has antifungal activity.
ţTN1774 أй½
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T2518ARRY-380 (analog )Inhibitor,HER1,EGFR,ARRY380 (analog ),Epidermal growth factor receptor,ARRY 380 (a
ARRY-380 is a potent and selective HER2 inhibitor.
ţT2518 أй½
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T23889CID-663143CID 663143
CID-663143 inhibits cancer cell growth and shows microtubule-binding activity.
ţT23889 أй½
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T11123DuP 105DuP 105
DuP 105 is an orally active oxazolidinone, a new class of synthetic antimicrobial agent with activity against gram-positive bacteria.
ţT11123 أй½
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TP1472Tyroserleutidetripeptide,Tyroserleutide,tumor,inhibit,Inhibitor,YSL,Antitumor
Tyroserleutide (YSL), isolated from the degradation products of porcine spleen, is a small molecular tripeptide which inhibits tumor growth both in vitro and in vivo.Tyroserleutide inhibits the growth and metastasis of human hepatocellular carcinoma (HCC).
ţTP1472 أй½
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T8630Baclofen hydrochlorideBaclofen hydrochloride,Gamma-aminobutyric acid Receptor,GABA,-Aminobutyric ac
Baclofen hydrochloride is a GAMMA-AMINOBUTYRIC ACID derivative that is a specific GABA-B RECEPTORS agonist. It is used in the treatment of MUSCLE SPASTICITY, especially that due to SPINAL CORD INJURIES. Its therapeutic effects result from actions at spinal and supraspinal sites, generally the reduction of excitatory transmission.
ţT8630 أй½
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TP1059Peptide YY (PYY) (3-36), humanNeuropeptide Y Receptor,Inhibitor,NPY receptor,Peptide YY (PYY) (336),
Peptide YY (PYY) (3-36), human is a gut hormone peptide. Peptide YY (PYY) (3-36), human acts as a Y2 receptor agonist to reduce appetite.
ţTP1059 أй½
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T7409360A360A,Telomerase,inhibit,Inhibitor,G-quadruplex
360A is a stabilizing G-Quadruplex ligand, and also inhibits telomerase activity for telomerase in TRAP-G4 assay(IC50 : 300 nM).
ţT7409 أй½
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T8003Methotrexate disodiumDNA/RNA Synthesis,WR19039 disodium,DNA,leukemia,immunosuppressant,reductase,ADC
Methotrexate disodium is an tetrahydrofolate dehydrogenase inhibitor
ţT8003 أй½
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T8631pyridostigminepyridostigmine
Pyridostigmine is an acetylcholinesterase inhibitor that can treat myasthenia gravis by increasing acetylcholine at the postsynaptic motor endplate.
ţT8631 أй½
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T7202ITEITE,Aryl Hydrocarbon Receptor,Inhibitor,inhibit,AhR
ITE is a potent endogenous agonist of aryl hydrocarbon receptor (AhR) (Ki : 3 nM), has immunosuppressive activity.
ţT7202 أй½
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T124455Batatasin V
Batatasin V is a natural product found in Stems and leaves of Dioscorea oppositifolia L
ţT124455 أй½
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T7549Talnetantschizophrenia,SB223412,NK receptor,Inhibitor,hNK-2,Talnetant,Neurokinin Receptor,Tachykinin
Talnetant is a selective, competitive, brain-penetrant NK3 receptor antagonist with the ability to modulate mesolimbic and mesocortical dopaminergic neurotransmission
ţT7549 أй½
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T7509PD 117519CI-947,PD-117519,Adenosine Receptor,Inhibitor,P1 receptor,PD117519,PD 117519,inhibit,CI 947
PD 117519 is an agonist of adenosine receptor
ţT7509 أй½
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T7626Budipinemonoamine oxidase type B (MAO-B),inhibit,CNS disorders,Parkinson disease,Budipine,Inhibitor,
Budipine is a low affinity, N-methyl-D-aspartate receptor antagonist,is an antiparkinsonian agent.
ţT7626 أй½
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T9140NAcM-OPT HCl(2089293-61-6 free base)NAcMOPT HCl(2089293616 free base),NAcM OPT HCl(2089293 61 6 free
NAcM-OPT HCL is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor that targets N-Acetyl-UBE2M (E2 conjugating enzyme, UBC12) interaction with DCN1 with IC50 of 79 nM.
ţT9140 أй½
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T20905Fludioxonil
Fludioxonil, a phenylpyrrole fungicide, inhibits the growth of B. cinerea from strawberry and blackberry crops.
ţT20905 أй½
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T6788Bitopertininhibit,Bitopertin,RG 1678,RO-4917838,RG-1678,GlyT,Inhibitor,RO 4917838,Glycine transporte
Bitopertin (RG1678, RO-4917838) is a potent inhibitor of glycine transporter 1 (GlyT1), with Ki of 8.1 nM for human hGlyT1b and IC50 of 22-25 nM in Chinese hamster ovary cells.
ţT6788 أй½
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T22737DMH4DMH4,DMH-4
DMH4 is a potent and selective inhibitor of VEGFR2 with an IC50 of 0.16 ?M.
ţT22737 أй½
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T9908PembrolizumabPembrolizumab
Pembrolizumab is a humanized monoclonal antibody inhibiting the PD-1 receptor and the first in the class of agents called the HER2 dimerization inhibitors that impairs the ability of HER2 to bind to other members of the HER family.
ţT9908 أй½