Syrosingopine |
An inhibitor of MCT1 and MCT4 (IC50s = 2,500 and 40 nM, respectively); inh… |
50 mg |
36402-50 |
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SZL P1-41 |
An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… |
10 mg |
26142-10 |
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SZL P1-41 |
An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… |
25 mg |
26142-25 |
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SZL P1-41 |
An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… |
5 mg |
26142-5 |
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SZL P1-41 |
An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… |
50 mg |
26142-50 |
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SZM-1209 |
A RIPK1 inhibitor; selectively binds to RIPK1 over RIPK3 (Kds = 85 and >10… |
1 mg |
38494-1 |
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SZM-1209 |
A RIPK1 inhibitor; selectively binds to RIPK1 over RIPK3 (Kds = 85 and >10… |
5 mg |
38494-5 |
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T0070907 |
A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… |
1 mg |
10026-1 |
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T0070907 |
A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… |
10 mg |
10026-10 |
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T0070907 |
A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… |
5 mg |
10026-5 |
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T0070907 |
A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… |
50 mg |
10026-50 |
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T0901317 |
A potent and selective agonist for both LXRα and LXRβ (EC50 = 5… |
10 mg |
71810-10 |
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T0901317 |
A potent and selective agonist for both LXRα and LXRβ (EC50 = 5… |
100 mg |
71810-100 |
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T0901317 |
A potent and selective agonist for both LXRα and LXRβ (EC50 = 5… |
50 mg |
71810-50 |
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T-1095 |
An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… |
10 mg |
37284-10 |
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T-1095 |
An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… |
100 mg |
37284-100 |
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T-1095 |
An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… |
5 mg |
37284-5 |
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T-1095 |
An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… |
50 mg |
37284-50 |
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T-5224 |
An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… |
1 mg |
22904-1 |
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T-5224 |
An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… |
10 mg |
22904-10 |
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T-5224 |
An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… |
25 mg |
22904-25 |
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T-5224 |
An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… |
5 mg |
22904-5 |
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T-5342126 |
A TLR4 antagonist; reduces LPS-induced NO production in RAW 264.7 cells (I… |
1 mg |
33099-1 |
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T-5342126 |
A TLR4 antagonist; reduces LPS-induced NO production in RAW 264.7 cells (I… |
10 mg |
33099-10 |
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T-5342126 |
A TLR4 antagonist; reduces LPS-induced NO production in RAW 264.7 cells (I… |
5 mg |
33099-5 |
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T5601640 |
An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… |
1 mg |
22140-1 |
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T5601640 |
An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… |
10 mg |
22140-10 |
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T5601640 |
An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… |
25 mg |
22140-25 |
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T5601640 |
An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… |
5 mg |
22140-5 |
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T-705 |
An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… |
10 mg |
23384-10 |
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T-705 |
An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… |
100 mg |
23384-100 |
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T-705 |
An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… |
25 mg |
23384-25 |
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T-705 |
An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… |
50 mg |
23384-50 |
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T-863 |
A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… |
1 mg |
25807-1 |
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T-863 |
A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… |
10 mg |
25807-10 |
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T-863 |
A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… |
25 mg |
25807-25 |
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T-863 |
A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… |
5 mg |
25807-5 |
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TA-01 |
An inducer of cardiomyocyte differentiation; increases expression of the c… |
1 mg |
24667-1 |
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TA-01 |
An inducer of cardiomyocyte differentiation; increases expression of the c… |
10 mg |
24667-10 |
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TA-01 |
An inducer of cardiomyocyte differentiation; increases expression of the c… |
25 mg |
24667-25 |
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TA-01 |
An inducer of cardiomyocyte differentiation; increases expression of the c… |
5 mg |
24667-5 |
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TA-02 |
An inducer of cardiomyocyte differentiation; increases expression of the c… |
10 mg |
24668-10 |
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TA-02 |
An inducer of cardiomyocyte differentiation; increases expression of the c… |
25 mg |
24668-25 |
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TA-02 |
An inducer of cardiomyocyte differentiation; increases expression of the c… |
5 mg |
24668-5 |
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T2AA (hydrochloride) |
An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… |
1 mg |
21921-1 |
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T2AA (hydrochloride) |
An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… |
10 mg |
21921-10 |
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T2AA (hydrochloride) |
An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… |
25 mg |
21921-25 |
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T2AA (hydrochloride) |
An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… |
5 mg |
21921-5 |
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Tabersonine |
An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… |
1 mg |
26848-1 |
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Tabersonine |
An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… |
10 mg |
26848-10 |
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Tabersonine |
An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… |
25 mg |
26848-25 |
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Tabersonine |
An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… |
5 mg |
26848-5 |
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TACA |
An agonist of homomeric GABAA receptors; binds to homomeric GABAA receptor… |
10 mg |
35217-10 |
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TACA |
An agonist of homomeric GABAA receptors; binds to homomeric GABAA receptor… |
5 mg |
35217-5 |
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Tacrine (hydrochloride) |
An AChE and butrylcholinesterase inhibitor (IC50s = 31 and 26.5 nM, respec… |
1000 mg |
70240-1 |
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Tacrine (hydrochloride) |
An AChE and butrylcholinesterase inhibitor (IC50s = 31 and 26.5 nM, respec… |
5000 mg |
70240-5 |
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Tadalafil |
A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… |
10 mg |
14024-10 |
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Tadalafil |
A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… |
100 mg |
14024-100 |
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Tadalafil |
A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… |
25 mg |
14024-25 |
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Tadalafil |
A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… |
50 mg |
14024-50 |
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Tadalafil-d3 |
An internal standard for the quantification of tadalafil by GC- or LC-MS, |
1 mg |
25030-1 |
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Tadalafil-d3 |
An internal standard for the quantification of tadalafil by GC- or LC-MS, |
5 mg |
25030-5 |
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TAE-1 |
A sym-triazine with diverse biological activities; inhibits in vitro A&bet… |
10 mg |
20464-10 |
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TAE-1 |
A sym-triazine with diverse biological activities; inhibits in vitro A&bet… |
5 mg |
20464-5 |
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TAE684 |
A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… |
1 mg |
17670-1 |
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TAE684 |
A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… |
10 mg |
17670-10 |
More Info
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TAE684 |
A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… |
5 mg |
17670-5 |
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TAE684 |
A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… |
50 mg |
17670-50 |
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Tafamidis |
A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… |
10 mg |
13694-10 |
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Tafamidis |
A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… |
25 mg |
13694-25 |
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Tafamidis |
A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… |
5 mg |
13694-5 |
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Tafamidis |
A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… |
50 mg |
13694-50 |
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Tafenoquine |
An antimalarial agent; active against multidrug-resistant clinical isolate… |
10 mg |
30673-10 |
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Tafenoquine |
An antimalarial agent; active against multidrug-resistant clinical isolate… |
25 mg |
30673-25 |
More Info
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Tafenoquine |
An antimalarial agent; active against multidrug-resistant clinical isolate… |
5 mg |
30673-5 |
More Info
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