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16
Angiogenesis
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19
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10
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20
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5
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17
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Products starting with 'T'
or product name starting with:
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H530501
T-00127-HEV1
featured
T-00127-HEV1, also known as PI4KIIIβ Inhibitor II, is a PI4KIIIβ Inhibitor. T-0012...
H406129
T0070907
featured
T0070907 was identified as a potent and selective PPARgamma antagonist. With an ap...
H125024
T007-1
T007-1 is a colchicine-targetedcovalentMDgA (Microtubule Degradation Agent)
H532801
T-0156 hydrochloride
T 0156 is a potent and selective inhibitor of phosphodiesterase type 5 (PDE5). It...
H526689
T-0201
T-0201, also known as TA 0201, is a highly potent, long-lasting, orally active and...
H462575
T025
T025 is an orally available and highly potent Cdc2-like kinase (CLK) inhibitor for...
H465882
T-036
T-036 is a potent GCS inhibitor.
H532802
T-0509
T-0509 is a selective β1-adrenoceptor agonist.
H130155
T0510-3657
T0510-3657 is a selective activator of GPR17, inhibiting cAMP levels, with potenti...
H558246
T-0632
T-0632 is a novel potent and selective CCKA receptor antagonist.
H535842
T 0757
T 0757 is a bioactive chemical.
H558247
T-0901317
featured
T-0901317, also known as T-1317; TO-091317; TO 901317, is a liver X receptor (LXR...
H573593
T-0902611 benzenesulfonate
T-0902611 benzenesulfonate is a cytomegalovirus replication inhibitor that may be ...
H558663
T1001
T1001 is an antagonist of hypoxia-inducible factor-2α subunit (HIF-2α) which displ...
H533362
T-10106
T-10106 is a novel potent PPARγ antagonist with much improved drug-like properties...
H510330
T-1095
featured
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs). ...
H530635
T-1095A
T-1095A is an active metabolite of T-1095. T-1095 is a potent and selective inhib...
H463459
T-1101 tosylate
featured
T-1101 tosylate is a Hec1/Nek2 (Highly expressed in cancer 1 / NIMA-related kinase...
H555278
T-1105
featured
T-1105 is a broad-spectrum antiviral inhibitor that demonstrates good activity for...
H464475
T111
T111 is a novel Highly Potent Inhibitor of Toxoplasma gondii Tachyzoites.
H532804
T1117
T1117 is a fluorescent form of AM 25. It displays CB1 ligands.
H123011
T-112
featured
T 112 is an estrogen-related receptor gamma (ERRγ) agonist.
H465761
T1-12
T1-12 is a Novel Antagonist of the Human Androgen Receptor Targeting the Activatio...
H561375
T145
T145 inhibits growth of Enterococcus faecalis, Staphylococcus aureus and Mycobacte...
H577310
T 1690
T 1690 is a biochemical.
H555877
T16Ainh-A01
new
featured
T16A(inh)-A01 is an aminophenylthiazole that inhibits transient TMEM16A-mediated c...
H562720
T16A(inh)-B01
T16A(inh)-B01 is a class B inhibitor of the Ca(2+)-activated Cl(-) Channel, Ano1(T...
H562719
T16A(inh)-C01
T16A(inh)-C01 is a class C inhibitor of the Ca(2+)-activated Cl(-) Channel, Ano1(T...
H562718
T16A(inh)-D01
T16A(inh)-D01 is a class D inhibitor of the Ca(2+)-activated Cl(-) Channel, Ano1(T...
H122724
T1742
T1742, also known as 4E 1RCat, is an autophagy Inhibitor by disrupting the Protein...
H585256
T1801 A
T1801 A is a derivative of a hydroquinone antibiotic and is active against Gram-po...
H526300
T-1840383
T-1840383 is a novel inhibitor of HGF-induced c-Met phosphorylation and VEGF-induc...
H577294
T-1973 methiodide
T-1973 methiodide is a biochemical.
H526946
T-2000
T-2000, also known as DMMDPB, is a GABA receptor agonist potentially for the treat...
H527709
T-2007
T-2007, also known as DPB and 5,5-Diphenylbarbituric acid, is an α-amino-3-hydroxy...
H532805
T-226296
T-226296 is a melanin concentrating hormone receptor 1 (MCHR1) antagonist.
H25146
T-2307
T-2307 is an aromatic diamidine currently in development for the treatment of inva...
H532806
T2328
T2328 is a bioactive chemical.
H563746
T2384
T2384 is an antidiabetic agent with unique peroxisome proliferator-activated recep...
H561310
T-26c
featured
T-26c is a highly potent, selective and cell-permeable matrix metalloproteinases 1...
H574927
T-26c disodium
featured
T-26c disodium is an MMP13 inhibitor..
H465999
T-271
T-271 is a novel selective mitophagy inducer of damaged mitochondria.
H465678
T-278
T-278 is a novel potent inhibitor of DGKγ (IC50 = 30 nM) with desirable physicoche...
H574919
T2AA
featured
T2AA is a proliferating cell nuclear antigen (PCNA) inhibitor that inhibits PCNA/P...
H565224
T2C-2
T2C-2 is a potent and highly selective nNOS inhibitor.
H581564
T-2 triol
featured
T-2 Mycotoxin is a trichothecene mycotoxin. It is a naturally occurring mold bypro...
H563179
T-3256336
T-3256336 is an orally available IAP antagonist. It act by selectively binding to ...
H526814
T-3364366
T-3364366 is a potent, reversible, slow-binding D5D inhibitor with D5D Ki < 2.7 n...
H562174
T-3775440 HCl
T-3775440 HCl is a potent, selecitve, irreversible LSD1 inhibitor.
H563966
T-3861174
T-3861174 is a prolyl tRNA synthetase (PRS) inhibitor, exhibiting significant in v...
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