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Cat. No. Product Name Field of Application Chemical Structure
DCAPI1463 Landiolol Hydrochloride Landiolol Hydrochloride
DC1108 Laninamivir (CS-8958) Featured Laninamivir (CS-8958) is a neuraminidase inhibitor which is being researched for the treatment and prophylaxis of Influenzavirus A and Influenzavirus B.
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.
DC23858 Lanraplenib (GS-9876) Featured Lanraplenib is a potent, selective Syk kinase inhibitor for treatment various disease states, including cancer and inflammatory conditions.
DC9091 Lansoprazole Lansoprazole(AG 1749) is a proton pump inhibitor which prevents the stomach from producing acid.
DC23502 L-AP4 Featured L-AP4 is a selective group III metabotropic glutamate receptor agonist..
DCAPI1512 Lapatinib Featured Lapatinib
DC3143 Lapatinib ditosylate Featured Lapatinib Ditosylate (GW572016, GW2016, Tykerb, Tyverb) is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 nM, respectively.
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.
DC2071 ABR-215062 (Laquinimod) Featured Laquinimod (ABR-215062) is a potent immunomodulator.
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.
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.
DC7710 Lasmiditan (COL-144; LY573144) Featured 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.
DCAPI1501 Lasofoxifene tartrate Featured Lasofoxifene Tartrate is a non-steroidal selective estrogen receptor modulator (SERM).
DC12443 LASV inhibitor 3.3 Featured 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
DC8635 Latanoprost Featured Latanoprost is a prodrug (isopropyl ester) of 17-phenyl-13,14-dihydro prostaglandin F2α.
DC12188 Lathosterol Featured Lathosterol is a cholesterol-like molecule. Serum Lathosterol concentration is an indicator of whole-body cholesterol synthesis.
DC10853 LAU159 Featured LAU159 is a novelα6β3γ2 GABAA receptor inhibitor.
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.
DC10598 lavendustin A Featured 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.
DC10597 lavendustin B Featured 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).
DC9512 Lazabemide Featured 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).
DC11900 Lazertinib Featured 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
DC7801 LB-100 Featured 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.
DC22765 LB-102 Featured LB-102 (LB-1.2, LB 102) is a a selective dopamine D2/3/5-HT7 inhibitor.
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..
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).
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..
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.
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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