CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 785 of 870
Non-Antibody Products
Page 785 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Syrosingopine | An inhibitor of MCT1 and MCT4 (IC50s = 2,500 and 40 nM, respectively); inh… | 50 mg | 36402-50 | More Info |
| SZL P1-41 | An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… | 10 mg | 26142-10 | More Info |
| SZL P1-41 | An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… | 25 mg | 26142-25 | More Info |
| SZL P1-41 | An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… | 5 mg | 26142-5 | More Info |
| SZL P1-41 | An inhibitor of Skp2; inhibits the interaction between Skp2 and Skp1 to bl… | 50 mg | 26142-50 | More Info |
| SZM-1209 | A RIPK1 inhibitor; selectively binds to RIPK1 over RIPK3 (Kds = 85 and >10… | 1 mg | 38494-1 | More Info |
| SZM-1209 | A RIPK1 inhibitor; selectively binds to RIPK1 over RIPK3 (Kds = 85 and >10… | 5 mg | 38494-5 | More Info |
| T0070907 | A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… | 1 mg | 10026-1 | More Info |
| T0070907 | A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… | 10 mg | 10026-10 | More Info |
| T0070907 | A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… | 5 mg | 10026-5 | More Info |
| T0070907 | A potent and selective PPARγ antagonist (apparent IC50 = 1 nM for th… | 50 mg | 10026-50 | More Info |
| T0901317 | A potent and selective agonist for both LXRα and LXRβ (EC50 = 5… | 10 mg | 71810-10 | More Info |
| T0901317 | A potent and selective agonist for both LXRα and LXRβ (EC50 = 5… | 100 mg | 71810-100 | More Info |
| T0901317 | A potent and selective agonist for both LXRα and LXRβ (EC50 = 5… | 50 mg | 71810-50 | More Info |
| T-1095 | An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… | 10 mg | 37284-10 | More Info |
| T-1095 | An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… | 100 mg | 37284-100 | More Info |
| T-1095 | An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… | 5 mg | 37284-5 | More Info |
| T-1095 | An SGLT1 and SGLT2 inhibitor (IC50s = 22.8 and 2.3 µM, respectively)… | 50 mg | 37284-50 | More Info |
| T-5224 | An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… | 1 mg | 22904-1 | More Info |
| T-5224 | An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… | 10 mg | 22904-10 | More Info |
| T-5224 | An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… | 25 mg | 22904-25 | More Info |
| T-5224 | An inhibitor of c-fos / AP-1; inhibits the DNA binding activity of c-fos /… | 5 mg | 22904-5 | More Info |
| T-5342126 | A TLR4 antagonist; reduces LPS-induced NO production in RAW 264.7 cells (I… | 1 mg | 33099-1 | More Info |
| T-5342126 | A TLR4 antagonist; reduces LPS-induced NO production in RAW 264.7 cells (I… | 10 mg | 33099-10 | More Info |
| T-5342126 | A TLR4 antagonist; reduces LPS-induced NO production in RAW 264.7 cells (I… | 5 mg | 33099-5 | More Info |
| T5601640 | An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… | 1 mg | 22140-1 | More Info |
| T5601640 | An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… | 10 mg | 22140-10 | More Info |
| T5601640 | An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… | 25 mg | 22140-25 | More Info |
| T5601640 | An inhibitor of LIMK2; reduces p-cofilin in Nf1-/- MEFs (IC50 = 30 µ… | 5 mg | 22140-5 | More Info |
| T-705 | An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… | 10 mg | 23384-10 | More Info |
| T-705 | An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… | 100 mg | 23384-100 | More Info |
| T-705 | An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… | 25 mg | 23384-25 | More Info |
| T-705 | An antiviral agent; inhibits influenza A, B, and C (IC50s = 0.013-0.48 &mi… | 50 mg | 23384-50 | More Info |
| T-863 | A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… | 1 mg | 25807-1 | More Info |
| T-863 | A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… | 10 mg | 25807-10 | More Info |
| T-863 | A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… | 25 mg | 25807-25 | More Info |
| T-863 | A DGAT-1 inhibitor (IC50 = 15 nM); selective for DGAT-1 over DGAT-2 and AC… | 5 mg | 25807-5 | More Info |
| TA-01 | An inducer of cardiomyocyte differentiation; increases expression of the c… | 1 mg | 24667-1 | More Info |
| TA-01 | An inducer of cardiomyocyte differentiation; increases expression of the c… | 10 mg | 24667-10 | More Info |
| TA-01 | An inducer of cardiomyocyte differentiation; increases expression of the c… | 25 mg | 24667-25 | More Info |
| TA-01 | An inducer of cardiomyocyte differentiation; increases expression of the c… | 5 mg | 24667-5 | More Info |
| TA-02 | An inducer of cardiomyocyte differentiation; increases expression of the c… | 10 mg | 24668-10 | More Info |
| TA-02 | An inducer of cardiomyocyte differentiation; increases expression of the c… | 25 mg | 24668-25 | More Info |
| TA-02 | An inducer of cardiomyocyte differentiation; increases expression of the c… | 5 mg | 24668-5 | More Info |
| T2AA (hydrochloride) | An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… | 1 mg | 21921-1 | More Info |
| T2AA (hydrochloride) | An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… | 10 mg | 21921-10 | More Info |
| T2AA (hydrochloride) | An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… | 25 mg | 21921-25 | More Info |
| T2AA (hydrochloride) | An inhibitor of PCNA; inhibits protein-protein interactions between PCNA a… | 5 mg | 21921-5 | More Info |
| Tabersonine | An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… | 1 mg | 26848-1 | More Info |
| Tabersonine | An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… | 10 mg | 26848-10 | More Info |
| Tabersonine | An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… | 25 mg | 26848-25 | More Info |
| Tabersonine | An indole alkaloid; inhibits Aβ42 fibril formation and disintegrates… | 5 mg | 26848-5 | More Info |
| TACA | An agonist of homomeric GABAA receptors; binds to homomeric GABAA receptor… | 10 mg | 35217-10 | More Info |
| TACA | An agonist of homomeric GABAA receptors; binds to homomeric GABAA receptor… | 5 mg | 35217-5 | More Info |
| Tacrine (hydrochloride) | An AChE and butrylcholinesterase inhibitor (IC50s = 31 and 26.5 nM, respec… | 1000 mg | 70240-1 | More Info |
| Tacrine (hydrochloride) | An AChE and butrylcholinesterase inhibitor (IC50s = 31 and 26.5 nM, respec… | 5000 mg | 70240-5 | More Info |
| Tadalafil | A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… | 10 mg | 14024-10 | More Info |
| Tadalafil | A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… | 100 mg | 14024-100 | More Info |
| Tadalafil | A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… | 25 mg | 14024-25 | More Info |
| Tadalafil | A PDE5 inhibitor (IC50 = 1.2 nM); selective for PDE5 over PDE1-4 and 7-10… | 50 mg | 14024-50 | More Info |
| Tadalafil-d3 | An internal standard for the quantification of tadalafil by GC- or LC-MS, | 1 mg | 25030-1 | More Info |
| Tadalafil-d3 | An internal standard for the quantification of tadalafil by GC- or LC-MS, | 5 mg | 25030-5 | More Info |
| TAE-1 | A sym-triazine with diverse biological activities; inhibits in vitro A&bet… | 10 mg | 20464-10 | More Info |
| TAE-1 | A sym-triazine with diverse biological activities; inhibits in vitro A&bet… | 5 mg | 20464-5 | More Info |
| TAE684 | A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… | 1 mg | 17670-1 | More Info |
| TAE684 | A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… | 10 mg | 17670-10 | More Info |
| TAE684 | A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… | 5 mg | 17670-5 | More Info |
| TAE684 | A selective ALK inhibitor that blocks the proliferation of ALCL-derived an… | 50 mg | 17670-50 | More Info |
| Tafamidis | A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… | 10 mg | 13694-10 | More Info |
| Tafamidis | A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… | 25 mg | 13694-25 | More Info |
| Tafamidis | A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… | 5 mg | 13694-5 | More Info |
| Tafamidis | A TTR kinetic stabilizer; binds to TTR with negative cooperativity (Kd1 =… | 50 mg | 13694-50 | More Info |
| Tafenoquine | An antimalarial agent; active against multidrug-resistant clinical isolate… | 10 mg | 30673-10 | More Info |
| Tafenoquine | An antimalarial agent; active against multidrug-resistant clinical isolate… | 25 mg | 30673-25 | More Info |
| Tafenoquine | An antimalarial agent; active against multidrug-resistant clinical isolate… | 5 mg | 30673-5 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
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http://www.caymanchem.com
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