DC9953 |
Leukadherin-1
Featured
|
Leukadherin-1 is a specific agonist of CR3 and the leukocyte surface integrin CD11b/CD18. |
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DC8688 |
Leupeptin hemisulfate
Featured
|
Leupeptin hemisulfate is a reversible, competitive serine/cysteine protease inhibitor, which has been shown to inhibit cathepsins B, H, L, and S, calpain, and trypsin. Leupeptin hemisulfate is an orally active, antioxidant and anti-inflammatory agent. |
|
DC8314 |
Leuprolide Acetate
Featured
|
Leuprolide acetate (Leuprorelin) is a GnRH analog; leuprolide acetate acts as an agonist at pituitary GnRH receptors. |
|
DC22504 |
Leuprorelin
Featured
|
Leuprorelin (Leuprolide) is a GnRH analog and agonist of GnRH receptor, interrupts the normal pulsatile stimulation and desensitizing of the GnRH receptors.. |
|
DCAPI1088 |
Levamisole HCl(Ergamisol) |
Levamisole HCl(Ergamisol) |
|
DCAPI1004 |
Levetiracetam |
Levetiracetam |
|
DC8714 |
Levobetaxolol hydrochloride
Featured
|
Levobetaxolol hydrochloride is a beta-adrenergic receptor inhibitor (beta blocker), used to lower the pressure in the eye in treating conditions such as glaucoma. |
|
DCAPI1518 |
Levobupivacaine HCL |
Levobupivacaine HCL |
|
DC8675 |
Levodropropizine |
Levodropropizine is a histamine receptor inhibitor, Levodropropizine is an effective and very well tolerated peripheral antitussive drug. |
|
DCAPI1002 |
Levofloxacin (Levaquin) |
Levofloxacin (Levaquin) |
|
DC10257 |
Levofloxacin hydrate |
Levofloxacin is a broad-spectrum, third-generation fluoroquinolone antibiotic and optically active L-isomer of ofloxacin with antibacterial activity. |
|
DCAPI1348 |
Levonorgestrel(Levonelle) |
Levonorgestrel(Levonelle) |
|
DCAPI1068 |
Levosimendan |
Levosimendan |
|
DC9075 |
Levosulpiride |
Levosulpiride is the (S)-enantiomer of sulpiride, which is a D2 receptor a antagonist, an atypical antipsychotic drug of the benzamide class. |
|
DCAPI1437 |
Lexacalcitol |
Lexacalcitol |
|
DC12384 |
LF3
Featured
|
LF3 is a specific inhibitor of canonical Wnt signaling by disrupting the interaction between β-catenin and TCF4 with an IC50 less than 2 μM. |
|
DC22727 |
LGB-321 |
LGB-321 (LGB321) is a potent and specific pan-Pim inhibitor with Ki of 1/2.1/0.8 pM for Pim1/2/3, respectively. |
|
DC22137 |
LGD2226
Featured
|
LGD-2226 (LGD2226) is an orally active, selective androgen receptor modulator (SARM) with binding Ki of 1 nM, >1000-fold selectivity over GR,PR, MR and ER. |
|
DC7633 |
Ligandrol (VK5211, LGD-4033)
Featured
|
Ligandrol (LGD-4033) is a novel nonsteroidal, oral SARM that binds to androgen receptor with high affinity (Ki of 1 nM) and selectivity. |
|
DC10278 |
LGD-6972
Featured
|
LGD-6972 is a selective and orally active glucagon receptor antagonist. LGD-6972 has the potential for type 2 diabetes research. |
|
DC25068 |
L-g-glutamyl-p-nitroanilide hydrochloride |
L-g-glutamyl-p-nitroanilide hydrochloride is a potent, competitive inhibitor of the neutral amino acid transporter ASCT2 (SLC1A5) with pKa of 13.79. |
|
DC7186 |
LGK-974
Featured
|
LGK-974 is a potent and specific PORCN inhibitor, and inhibits Wnt signaling with IC50 of 0.4 nM. |
|
DC9895 |
L-Glutamic acid monosodium salt |
L-Glutamic acid monosodium salt is the sodium salt of glutamic acid, found naturally in tomatoes, cheese and other foods. |
|
DC7018 |
LGX-818(Encorafenib)
Featured
|
LGX818 is an orally available mutated BRaf V600E inhibitor(IC50=0.3 nM) with potential antineoplastic activity. |
|
DC10147 |
LH-21
Featured
|
LH 21 is a 1,2,4-triazole that acts as a cannabimimetic. |
|
DC7454 |
LH846
Featured
|
LH846 is a selective inhibitor of CK1δ (IC50 values are 290 nM, 1.3 uM and 2.5 uM for CK1δ, ε and α); displays no inhibitory activity at CK2. |
|
DC12206 |
L-Hexanoylcarnitine
Featured
|
L-Hexanoylcarnitine is an acylcarnitine and is found to be associated with celiac disease. |
|
DC12612 |
LHF-535 |
LHF-535 (LHF535, LHF 535) is a small-molecule viral entry inhibitor that targets the arenavirus envelope glycoprotein, exhibits potent antiviral activity against a broad array of hemorrhagic fever arenaviruses with IC50 of 0.1-0.3 nM. |
|
DC10312 |
L-Homocysteine thiolactone hydrochloride |
L-Homocysteine thiolactone hydrochloride is an intramolecular thioester of homocysteine; prevents translational incorporation of homocysteine into proteins. |
|
DC8751 |
Licofelone |
Licofelone is a dual COX/LOX inhibitor being considered as a treatment for osteoarthritis. |
|