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19
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Products starting with 'L'
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H319516
Lomitapide free base
featured
Lomitapide is a MTP inhibitor. Lomitapid is a novel agent for the treatment of homozygous familial h…
H407219
LY303511
featured
LY303511, also known as NV-128 and EM 101, is a potent mTOR inhibitor. LY303511 enhances TRAIL sen…
H407218
LY2409881
featured
LY2409881 is a potent and selective IKK2 inhibitor. LY2409881 potently synergizes with histone deac…
H407215
LY3000328
featured
LY3000328 is a Cathepsin S inhibitor with excellent in vitro potency and selectivity against other c…
H407201
LGH447 free base
featured
PIM447, also known as LGH447, is a potent Moloney murine leukemia (PIM) 1, 2, and 3 kinase inhibitor…
H522472
LY2886721
featured
LY2886721 is a potent and selective BACE1 inhibitor. LY2886721 elicits robust central Aβ pharmacodyn…
H317148
Lorediplon
featured
Lorediplon is a nonbenzodiazepine of the pyrazolopyrimidine family that is being pursued as a treatm…
H407188
LDC1267
featured
LDC1267 is a potent and selective TAM kinase inhibitor. LDC1267 displays lower activity against Met,…
H407184
LRRK2-IN-1
featured
LRRK2-IN-1 is a potent and selective inhibitor of leucine-rich repeat kinase 2 (LRRK2). LRRK2-IN-1 …
H522452
LX7101 free base
featured
LX7101 is a pyrrolopyrimidine-based, topically-delivered inhibitor of LIM domain kinase 2 (LIMK2), a…
H522414
Lanabecestat HCl
Lanabecestat, also known as AZD3293 and LY3314814, is a potent, highly permeable, orally active, blo…
H317122
Loxiglumide
featured
Loxiglumide is a potent, orally active, and selective CCK-A receptor antagonist which stimulates cal…
H522377
Ligandrol
featured
Ligandrol, also known as VK5211, LGD-4033, is a novel nonsteroidal oral selective androgen receptor…
H610225
LZN86178
featured
LZN86178, also known as BPD-Ring B and benzoporphyrin Ring B derivative, is a product from the synth…
H522372
LEO-29102
LEO-29102 is a potent, selective, and soft-drug phosphodiesterase 4 (PDE4) inhibitor, which may b…
H407124
LCRF-0004
LCRF-0004 is a potent and selective RON receptor tyrosine kinase inhibitor. The RON receptor tyrosi…
H522354
LY310762 HCl
featured
LY310762 is a 5-HT1D antagonist with Ki of 249 nM, having a weaker affinity for 5-HT1B receptor.
H510293
LY2979165
LY2979165 is a drug candidae that may be useful in the treatment of bipolar disorder. LY2979165 is b…
H510255
LXR623
featured
LXR623, also known as WAY-252623, is a highly selective and orally bioavailable synthetic modulator …
H501010
Lamivudine-galactose
Lamivudine-galactose is a lamivudine conjugate with galactose. Lamivudine (2',3'-dideoxy-3'-thiacyti…
H500910
L685458
featured
L685458 is a potent and selective γ -secretase inhibitor (IC50 = 17 nM) that displays > 50-fold sele…
H510222
L006235
featured
L006235, also called L235, is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that disp…
H314232
Lurasidone
featured
Lurasidone is a new atypical antipsychotic. It is also approved for the treatment of depressive epis…
H314230
Lucinactant
Lucinactant (trade name Surfaxin) is a liquid medication used to treat Infant Respiratory Distress S…
H300125
Linagliptin
featured
Linagliptin, also known as BI-1356, is a DPP-4 inhibitor developed by Boehringer Ingelheim for treat…
H314227
Linaclotide
featured
Linaclotide is an peptide agonist of guanylate cyclase 2C that is undergoing clinical trials for use…
H314253
Ledipasvir
featured
Ledipasvir, also known as GS-5885; is an inhibitor of the hepatitis C virus NS5A protein and is a dr…
H300220
Latrepirdine HCl
new
featured
Latrepirdine, also known as dimebolin (sold as Dimebon), is an antihistamine drug which has been use…
H406116
Lificiguat
featured
Lificiguat, also known as YC-1, is a inhibitor of Hypoxia-inducible factor-1alpha (HIF-1alpha). YC-1…
H401550
LY2109761
featured
LY2109761 is a novel transforming growth factor beta receptor type I and type II dual inhibitor. The…
H406381
LY83583
featured
LY83583 is a Msp1 inhibitor, a guanylate cyclase inhibitor and a cGMP modulator. LY83583 inhibits so…
H406115
LQB-118
LQB-118 is an orally active pterocarpanquinone molecule with potential anticancer activity. LQB-118 …
H406112
LLL12
LLL12 is a potent STAT3 inhibitor. LLL12 inhibits colony formation and cell migration and works syne…
H406588
LGB-321 HCl
LGB-321 is a potent and selective ATP-competitive small molecule inhibitor of PIM kinases (Pan-PIM k…
H401531
LFM-A13
featured
LFM-A13 is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK). LFM-A13 may be useful…
H406274
LCH-7749944
LCH-7749944, also known as GNF-Pf-2356, is a novel and potent PAK4 inhibitor, which effectively supp…
H406185
LBW242
LBW242 is a Smac mimetic, and potent IAP inhibitor. LBW242 is effective against mutant FLT3 at doses…
H406419
LB42908
LB42908 is a highly potent Ras farnesyltransferase inhibitor(IC(50)=0.9 nM against H-Ras and 2.4 nM …
H406301
L-744832
L-744832, also known as L-744,832, is a potent Farnesyltransferase inhibitor with potential anticanc…
H406368
L-2286
L-2286 is a novel PARP inhibitor. L-2286 exerted significant protective effect against ischemia-repe…
H206161
LY3009120
featured
LY3009120, also known as DP-4978, is potent and selective pan-RAF inhibitor with potential anticance…
H205855
LY3007113
LY3007113 is an orally active p38 mitogen-activated protein kinase (MAPK) inhibitor with potential i…
H201795
LY294002
featured
LY294002 is a morpholine derivative of quercetin. It is a potent inhibitor of phosphoinositide 3-kin…
H205527
LY2874455
featured
LY2874455 is a novel and potent FGF/FGFR Inhibitor. It exhibits a potent activity against FGF/FGFR-m…
H205525
LY2780301
LY2780301 is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein ki…
H206068
LY2510924
LY2510924 is an inhibitor of CXC chemokine receptor 4 (CXCR4), with potential antineoplastic activit…
H205925
LY2457546
LY2457546 is a potent and orally bioavailable inhibitor of multiple receptor tyrosine kinases involv…
H201792
LY2334737
featured
LY2334737 is an orally available valproic acid ester of gemcitabine, a broad-spectrum antimetabolite…
H205783
Lurtotecan
featured
Lurtotecan, also known as OSI-221 and NX-211, is a semisynthetic analogue of camptothecin and a pot…
H201780
Lucanthone
Lucanthone is orally available thioxanthone-based DNA intercalator and inhibitor of the DNA repair e…
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