LY3000328 |
A potent cathepsin S inhibitor (IC50 = 7.7 nM for the human enzyme); selec… |
500 µg |
29729-500 |
More Info
|
LY3009120 |
An inhibitor of A-Raf, B-Raf, and c-Raf (IC50s = 44, 31-47, and 42 nM, res… |
10 mg |
21504-10 |
More Info
|
LY3009120 |
An inhibitor of A-Raf, B-Raf, and c-Raf (IC50s = 44, 31-47, and 42 nM, res… |
25 mg |
21504-25 |
More Info
|
LY3009120 |
An inhibitor of A-Raf, B-Raf, and c-Raf (IC50s = 44, 31-47, and 42 nM, res… |
5 mg |
21504-5 |
More Info
|
LY3009120 |
An inhibitor of A-Raf, B-Raf, and c-Raf (IC50s = 44, 31-47, and 42 nM, res… |
50 mg |
21504-50 |
More Info
|
LY310762 |
A 5-HT1D antagonist; selective over 5-HT1B, where it inhibits binding of r… |
10 mg |
22938-10 |
More Info
|
LY310762 |
A 5-HT1D antagonist; selective over 5-HT1B, where it inhibits binding of r… |
25 mg |
22938-25 |
More Info
|
LY310762 |
A 5-HT1D antagonist; selective over 5-HT1B, where it inhibits binding of r… |
5 mg |
22938-5 |
More Info
|
LY311727 |
An inhibitor of Group IIA sPLA2 (IC50 = 0.47 µM) that interacts with… |
1 mg |
17973-1 |
More Info
|
LY311727 |
An inhibitor of Group IIA sPLA2 (IC50 = 0.47 µM) that interacts with… |
10 mg |
17973-10 |
More Info
|
LY311727 |
An inhibitor of Group IIA sPLA2 (IC50 = 0.47 µM) that interacts with… |
5 mg |
17973-5 |
More Info
|
LY315920 |
An inhibitor of hGIIA sPLA2 (IC50 = 9 nM), as well as mouse GIIA (mGIIA),… |
10 mg |
18267-10 |
More Info
|
LY315920 |
An inhibitor of hGIIA sPLA2 (IC50 = 9 nM), as well as mouse GIIA (mGIIA),… |
25 mg |
18267-25 |
More Info
|
LY315920 |
An inhibitor of hGIIA sPLA2 (IC50 = 9 nM), as well as mouse GIIA (mGIIA),… |
5 mg |
18267-5 |
More Info
|
LY315920 |
An inhibitor of hGIIA sPLA2 (IC50 = 9 nM), as well as mouse GIIA (mGIIA),… |
50 mg |
18267-50 |
More Info
|
LY3177833 |
An inhibitor of Cdc7 kinase (IC50 = 3.3 nM); inhibits phosphorylation of M… |
10 mg |
25988-10 |
More Info
|
LY3177833 |
An inhibitor of Cdc7 kinase (IC50 = 3.3 nM); inhibits phosphorylation of M… |
25 mg |
25988-25 |
More Info
|
LY3177833 |
An inhibitor of Cdc7 kinase (IC50 = 3.3 nM); inhibits phosphorylation of M… |
5 mg |
25988-5 |
More Info
|
LY3177833 |
An inhibitor of Cdc7 kinase (IC50 = 3.3 nM); inhibits phosphorylation of M… |
50 mg |
25988-50 |
More Info
|
LY3200882 |
An inhibitor of TGF-βRI; inhibits TGF-β-induced SMAD phosphoryla… |
1 mg |
25276-1 |
More Info
|
LY3200882 |
An inhibitor of TGF-βRI; inhibits TGF-β-induced SMAD phosphoryla… |
10 mg |
25276-10 |
More Info
|
LY3200882 |
An inhibitor of TGF-βRI; inhibits TGF-β-induced SMAD phosphoryla… |
25 mg |
25276-25 |
More Info
|
LY3200882 |
An inhibitor of TGF-βRI; inhibits TGF-β-induced SMAD phosphoryla… |
5 mg |
25276-5 |
More Info
|
LY320135 |
A cannabinoid CB1 receptor antagonist (Kis = 224 and >10,000 nM for CB1 an… |
1 mg |
11738-1 |
More Info
|
LY320135 |
A cannabinoid CB1 receptor antagonist (Kis = 224 and >10,000 nM for CB1 an… |
10 mg |
11738-10 |
More Info
|
LY320135 |
A cannabinoid CB1 receptor antagonist (Kis = 224 and >10,000 nM for CB1 an… |
5 mg |
11738-5 |
More Info
|
LY3214996 |
An ERK1 / 2 inhibitor (IC50 = 5 nM for both); inhibits cell proliferation… |
1 mg |
27936-1 |
More Info
|
LY3214996 |
An ERK1 / 2 inhibitor (IC50 = 5 nM for both); inhibits cell proliferation… |
10 mg |
27936-10 |
More Info
|
LY3214996 |
An ERK1 / 2 inhibitor (IC50 = 5 nM for both); inhibits cell proliferation… |
25 mg |
27936-25 |
More Info
|
LY3214996 |
An ERK1 / 2 inhibitor (IC50 = 5 nM for both); inhibits cell proliferation… |
5 mg |
27936-5 |
More Info
|
LY3381916 |
An IDO1 inhibitor; binds to apo-IDO1 |
1 mg |
33178-1 |
More Info
|
LY3381916 |
An IDO1 inhibitor; binds to apo-IDO1 |
10 mg |
33178-10 |
More Info
|
LY3381916 |
An IDO1 inhibitor; binds to apo-IDO1 |
25 mg |
33178-25 |
More Info
|
LY3381916 |
An IDO1 inhibitor; binds to apo-IDO1 |
5 mg |
33178-5 |
More Info
|
LY341495 |
A potent and selective antagonist of the group II metabotropic glutamate r… |
1 mg |
14693-1 |
More Info
|
LY341495 |
A potent and selective antagonist of the group II metabotropic glutamate r… |
10 mg |
14693-10 |
More Info
|
LY341495 |
A potent and selective antagonist of the group II metabotropic glutamate r… |
50 mg |
14693-50 |
More Info
|
LY345899 |
An MTHFD inhibitor ((IC50s = 96 and 663 nM for MTHFD1 and MTHFD2, respecti… |
1 mg |
36627-1 |
More Info
|
LY345899 |
An MTHFD inhibitor ((IC50s = 96 and 663 nM for MTHFD1 and MTHFD2, respecti… |
10 mg |
36627-10 |
More Info
|
LY345899 |
An MTHFD inhibitor ((IC50s = 96 and 663 nM for MTHFD1 and MTHFD2, respecti… |
25 mg |
36627-25 |
More Info
|
LY345899 |
An MTHFD inhibitor ((IC50s = 96 and 663 nM for MTHFD1 and MTHFD2, respecti… |
5 mg |
36627-5 |
More Info
|
LY354740 |
A group II mGluR agonist (Kis = 99 and 94 nM, respectively); inhibits fors… |
1 mg |
24215-1 |
More Info
|
LY354740 |
A group II mGluR agonist (Kis = 99 and 94 nM, respectively); inhibits fors… |
10 mg |
24215-10 |
More Info
|
LY354740 |
A group II mGluR agonist (Kis = 99 and 94 nM, respectively); inhibits fors… |
5 mg |
24215-5 |
More Info
|
LY364947 |
A selective inhibitor of TGF-β RI, with an IC50 value of 59 nM; poorl… |
10 mg |
13341-10 |
More Info
|
LY364947 |
A selective inhibitor of TGF-β RI, with an IC50 value of 59 nM; poorl… |
25 mg |
13341-25 |
More Info
|
LY364947 |
A selective inhibitor of TGF-β RI, with an IC50 value of 59 nM; poorl… |
5 mg |
13341-5 |
More Info
|
LY364947 |
A selective inhibitor of TGF-β RI, with an IC50 value of 59 nM; poorl… |
50 mg |
13341-50 |
More Info
|
LY379268 |
A group II mGluR inhibitor (EC50s = 2.69 and 4.48 nM, respectively for mGl… |
1 mg |
15351-1 |
More Info
|
LY379268 |
A group II mGluR inhibitor (EC50s = 2.69 and 4.48 nM, respectively for mGl… |
10 mg |
15351-10 |
More Info
|
LY379268 |
A group II mGluR inhibitor (EC50s = 2.69 and 4.48 nM, respectively for mGl… |
5 mg |
15351-5 |
More Info
|
LY393558 |
A serotonin reuptake inhibitor (IC50 = 3.3 nM in rat cortical synaptosomes… |
1 mg |
32775-1 |
More Info
|
LY393558 |
A serotonin reuptake inhibitor (IC50 = 3.3 nM in rat cortical synaptosomes… |
10 mg |
32775-10 |
More Info
|
LY393558 |
A serotonin reuptake inhibitor (IC50 = 3.3 nM in rat cortical synaptosomes… |
5 mg |
32775-5 |
More Info
|
LY404039 |
A potent agonist of mGluR2 and mGluR3 (Kis = 149 and 62 nM, respectively);… |
1 mg |
18408-1 |
More Info
|
LY404039 |
A potent agonist of mGluR2 and mGluR3 (Kis = 149 and 62 nM, respectively);… |
10 mg |
18408-10 |
More Info
|
LY404039 |
A potent agonist of mGluR2 and mGluR3 (Kis = 149 and 62 nM, respectively);… |
25 mg |
18408-25 |
More Info
|
LY404039 |
A potent agonist of mGluR2 and mGluR3 (Kis = 149 and 62 nM, respectively);… |
5 mg |
18408-5 |
More Info
|
LY404187 |
A benzothiadiazide positive allosteric modulator of AMPA receptors; increa… |
10 mg |
28741-10 |
More Info
|
LY404187 |
A benzothiadiazide positive allosteric modulator of AMPA receptors; increa… |
25 mg |
28741-25 |
More Info
|
LY404187 |
A benzothiadiazide positive allosteric modulator of AMPA receptors; increa… |
5 mg |
28741-5 |
More Info
|
LY404187 |
A benzothiadiazide positive allosteric modulator of AMPA receptors; increa… |
50 mg |
28741-50 |
More Info
|
LY411575 |
A cell-permeable γ-secretase inhibitor (IC50 = 0.14 nM) that has bee… |
1 mg |
16162-1 |
More Info
|
LY411575 |
A cell-permeable γ-secretase inhibitor (IC50 = 0.14 nM) that has bee… |
10 mg |
16162-10 |
More Info
|
LY411575 |
A cell-permeable γ-secretase inhibitor (IC50 = 0.14 nM) that has bee… |
25 mg |
16162-25 |
More Info
|
LY411575 |
A cell-permeable γ-secretase inhibitor (IC50 = 0.14 nM) that has bee… |
5 mg |
16162-5 |
More Info
|
LY433771 |
An inhibitor of type X sPLA2 (IC50 = 3 nM) |
1 mg |
35406-1 |
More Info
|
LY433771 |
An inhibitor of type X sPLA2 (IC50 = 3 nM) |
10 mg |
35406-10 |
More Info
|
LY433771 |
An inhibitor of type X sPLA2 (IC50 = 3 nM) |
5 mg |
35406-5 |
More Info
|
LY83583 |
LY83583 is an inhibitor of soluble guanylate cyclase and of cGMP productio… |
1 mg |
70230-1 |
More Info
|
LY83583 |
LY83583 is an inhibitor of soluble guanylate cyclase and of cGMP productio… |
10 mg |
70230-10 |
More Info
|
LY83583 |
LY83583 is an inhibitor of soluble guanylate cyclase and of cGMP productio… |
5 mg |
70230-5 |
More Info
|
LY83583 |
LY83583 is an inhibitor of soluble guanylate cyclase and of cGMP productio… |
50 mg |
70230-50 |
More Info
|
Lycopene |
A red-colored carotenoid found in tomatoes and other red fruits and vegeta… |
1 mg |
70945-1 |
More Info
|
Lycopene |
A red-colored carotenoid found in tomatoes and other red fruits and vegeta… |
10 mg |
70945-10 |
More Info
|
Lycopene |
A red-colored carotenoid found in tomatoes and other red fruits and vegeta… |
5 mg |
70945-5 |
More Info
|
Lycorine |
An alkaloid with diverse biological activities; active against P. falcipar… |
10 mg |
30650-10 |
More Info
|
Lycorine |
An alkaloid with diverse biological activities; active against P. falcipar… |
25 mg |
30650-25 |
More Info
|
Lycorine |
An alkaloid with diverse biological activities; active against P. falcipar… |
5 mg |
30650-5 |
More Info
|
Lycorine |
An alkaloid with diverse biological activities; active against P. falcipar… |
50 mg |
30650-50 |
More Info
|
Lydicamycin |
An antibiotic that is particularly cytotoxic against S. aureus, including… |
2.5 mg |
20584-25 |
More Info
|
Lydicamycin |
An antibiotic that is particularly cytotoxic against S. aureus, including… |
500 µg |
20584-500 |
More Info
|
LYG-202 |
A synthetic flavonoid with anticancer and anti-angiogenic activity; inhibi… |
1 mg |
21976-1 |
More Info
|
LYG-202 |
A synthetic flavonoid with anticancer and anti-angiogenic activity; inhibi… |
10 mg |
21976-10 |
More Info
|
LYG-202 |
A synthetic flavonoid with anticancer and anti-angiogenic activity; inhibi… |
25 mg |
21976-25 |
More Info
|
LYG-202 |
A synthetic flavonoid with anticancer and anti-angiogenic activity; inhibi… |
5 mg |
21976-5 |
More Info
|
LY2365109 (hydrochloride) |
An inhibitor of GlyT1a (IC50 = 15.8 nM in BE2-C cells expressing the human… |
10 mg |
37427-10 |
More Info
|
LY2365109 (hydrochloride) |
An inhibitor of GlyT1a (IC50 = 15.8 nM in BE2-C cells expressing the human… |
25 mg |
37427-25 |
More Info
|
LY2365109 (hydrochloride) |
An inhibitor of GlyT1a (IC50 = 15.8 nM in BE2-C cells expressing the human… |
5 mg |
37427-5 |
More Info
|
LY2365109 (hydrochloride) |
An inhibitor of GlyT1a (IC50 = 15.8 nM in BE2-C cells expressing the human… |
50 mg |
37427-50 |
More Info
|
LY266097 (hydrochloride) |
A 5-HT2B receptor antagonist (Ki = 0.5 nM); selective for 5-HT2B over 5-HT… |
1 mg |
11935-1 |
More Info
|
LY266097 (hydrochloride) |
A 5-HT2B receptor antagonist (Ki = 0.5 nM); selective for 5-HT2B over 5-HT… |
10 mg |
11935-10 |
More Info
|
LY266097 (hydrochloride) |
A 5-HT2B receptor antagonist (Ki = 0.5 nM); selective for 5-HT2B over 5-HT… |
5 mg |
11935-5 |
More Info
|
LY266097 (hydrochloride) |
A 5-HT2B receptor antagonist (Ki = 0.5 nM); selective for 5-HT2B over 5-HT… |
500 µg |
11935-500 |
More Info
|
LY303511 (hydrochloride) |
An inhibitor of mTOR-dependent phosphorylation of S6K; reduces cell prolif… |
1 mg |
15514-1 |
More Info
|
LY303511 (hydrochloride) |
An inhibitor of mTOR-dependent phosphorylation of S6K; reduces cell prolif… |
5 mg |
15514-5 |
More Info
|
LY333531 (hydrochloride) |
A PKCβ inhibitor (IC50s = 4.7 and 5.9 nM for PKCβ1 and PKCβ… |
1 mg |
13964-1 |
More Info
|
LY333531 (hydrochloride) |
A PKCβ inhibitor (IC50s = 4.7 and 5.9 nM for PKCβ1 and PKCβ… |
5 mg |
13964-5 |
More Info
|
LY334370 (hydrochloride) |
A 5-HT1F receptor agonist (Kd =0.446 nM); selective for 5-HT1F over other… |
1 mg |
29481-1 |
More Info
|
LY334370 (hydrochloride) |
A 5-HT1F receptor agonist (Kd =0.446 nM); selective for 5-HT1F over other… |
10 mg |
29481-10 |
More Info
|