DCAPI1463 |
Landiolol Hydrochloride |
Landiolol Hydrochloride |
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DC1108 |
Laninamivir (CS-8958)
Featured
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Laninamivir (CS-8958) is a neuraminidase inhibitor which is being researched for the treatment and prophylaxis of Influenzavirus A and Influenzavirus B. |
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DC23824 |
Lanperisone |
Lanperisone (NK 433) is a centrally acting muscle relaxant that selectively kills of K-ras mutant cancer cells in a cell cycle-independent fashion. |
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DC23858 |
Lanraplenib (GS-9876)
Featured
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Lanraplenib is a potent, selective Syk kinase inhibitor for treatment various disease states, including cancer and inflammatory conditions. |
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DC9091 |
Lansoprazole |
Lansoprazole(AG 1749) is a proton pump inhibitor which prevents the stomach from producing acid. |
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DC23502 |
L-AP4
Featured
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L-AP4 is a selective group III metabotropic glutamate receptor agonist.. |
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DCAPI1512 |
Lapatinib
Featured
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Lapatinib |
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DC3143 |
Lapatinib ditosylate
Featured
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Lapatinib Ditosylate (GW572016, GW2016, Tykerb, Tyverb) is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 nM, respectively. |
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DC9433 |
Lapatinib (ditosylate) |
Lapatinib ditosylate(GW-572016 ditosylate) is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 nM, respectively.
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DC2071 |
ABR-215062 (Laquinimod)
Featured
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Laquinimod (ABR-215062) is a potent immunomodulator. |
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DCAPI1019 |
L-Arginine HCl |
L-Arginine is the nitrogen donor for synthesis of nitric oxide, a potent vasodilator that is deficient during times of sickle cell crisis. |
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DC12472 |
LAS195319 |
LAS195319 (LAS-195319) is a potent, selective, inhaled PI3Kδ inhibitor with IC50 of 0.5 nM, weakly inhibits PI3Kβ and γ (>20-fold), no activity against PI3Kα. |
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DC7710 |
Lasmiditan (COL-144; LY573144)
Featured
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Lasmiditan (COL-144; LY573144) is a high-affinity, highly selective 5-HT1F receptor agonist(Ki=2.1 nM), compared with Ki of 1043 nM and 1357 nM at the 5-HT(1B) and 5-HT(1D) receptors, respectively. |
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DCAPI1501 |
Lasofoxifene tartrate
Featured
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Lasofoxifene Tartrate is a non-steroidal selective estrogen receptor modulator (SERM). |
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DC12443 |
LASV inhibitor 3.3
Featured
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LASV inhibitor 3.3 (LAMP1 inhibitor 3.3) is a specific inhibitor of Lassa fever virus (LASV, IC50=1.8 uM), inhibits LASV GP-mediated infection and cross-links to the LASV receptor, LAMP1, in cells; does not inhibits the GP-mediated infection of LCMV, LuJo |
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DC8635 |
Latanoprost
Featured
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Latanoprost is a prodrug (isopropyl ester) of 17-phenyl-13,14-dihydro prostaglandin F2α. |
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DC12188 |
Lathosterol
Featured
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Lathosterol is a cholesterol-like molecule. Serum Lathosterol concentration is an indicator of whole-body cholesterol synthesis. |
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DC10853 |
LAU159
Featured
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LAU159 is a novelα6β3γ2 GABAA receptor inhibitor. |
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DC9877 |
Lauric Acid |
Lauric Acid is a saturated medium-chain fatty acid with a 12-carbon backbone. Lauric acid is found naturally in various plant and animal fats and oils, and is a major component of coconut oil and palm kernel oil. |
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DC10598 |
lavendustin A
Featured
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Lavendustin A is a selective inhibitor of epidermal growth factor (EGF) receptor-associated tyrosine kinase (IC50 = 11 nM) that was first isolated from a Streptomyces culture filtrate. |
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DC10597 |
lavendustin B
Featured
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Lavendustin B is a Tyrosine Kinase Inhibitor amd an inhibitor of HIV-1 integrase (IN) interaction with its cognate cellular cofactor, lens epithelium-derived growth factor (LEDGF/p75). |
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DC9512 |
Lazabemide
Featured
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Lazabemide(Ro 19-6327/000) is selective, reversible monoamine oxidase B (MAO-B) inhibitor (IC50 values are 0.03 and > 100 μM for MAO-B and MAO-A respectively).
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DC11900 |
Lazertinib
Featured
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Lazertinib (YH25448, GNS-1480) is a highly potent, mutant-selective, irreversible, brain-penetrant and orally active EGFR tyrosine-kinase inhibitors for both the T790M mutation and activating EGFR mutations |
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DC7801 |
LB-100
Featured
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LB-100 is a small-molecular protein phosphatase 2A(PP2A)inhibitor with IC50 of 0.85 μM and 3.87 μM in BxPc-3 and Panc-1 cells. |
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DC22765 |
LB-102
Featured
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LB-102 (LB-1.2, LB 102) is a a selective dopamine D2/3/5-HT7 inhibitor. |
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DC21221 |
LB42908 |
LB42908 is a highly potent, selective, orally active inhibitor of Ras farnesyltransferase (FTase) with IC50 of 0.9 nM against H-Ras and 2.4 nM against K-Ras.. |
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DC21219 |
LBL1 |
LBL1 (Lamin A inhibitor LBL1) is a novel pyrroloquinazoline compound with significant anticancer activity, targets nuclear lamins and binds to the coiled-coil domain of lamin A (Kd=5.11 uM). |
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DC22135 |
LC-1028 |
LC-1028 (LC1028) is a novel potent selective, covalent and irreversible inhibitor of p97 (valosin-containing protein), remains essentially irreversible ac tivity against p97 mutant C522A.. |
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DC21222 |
LCB 03-0110 |
LCB 03-0110 is a potent, ATP-competitive inhibitor of Discoidin domain receptor (DDR) family and c-Src tyrosine kinase family, as well as Btk and Syk. |
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DC21223 |
LCB 03-0110 dihydrochloride |
LCB 03-0110 is a potent, ATP-competitive inhibitor of Discoidin domain receptor (DDR) family and c-Src tyrosine kinase family, as well as Btk and Syk. |
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