TCEP-biotin |
An affinity probe for protein lysine crotonylation; addition of the TCEP m… |
1 mg |
25365-1 |
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TCEP-biotin |
An affinity probe for protein lysine crotonylation; addition of the TCEP m… |
500 µg |
25365-500 |
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TCEP (hydrochloride) |
An odorless, selective, and water-soluble reducing agent that is commonly… |
1 g |
14329-1 |
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TC-FPR 43 |
An agonist of FPR1 and FPR2; induces calcium flux in CHO cells expressing… |
10 mg |
29804-10 |
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TC-FPR 43 |
An agonist of FPR1 and FPR2; induces calcium flux in CHO cells expressing… |
25 mg |
29804-25 |
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TC-FPR 43 |
An agonist of FPR1 and FPR2; induces calcium flux in CHO cells expressing… |
5 mg |
29804-5 |
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TC-FPR 43 |
An agonist of FPR1 and FPR2; induces calcium flux in CHO cells expressing… |
50 mg |
29804-50 |
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TC 2559 (fumarate) |
A partial agonist for α4β2 subunit-containing nAChRs (EC50 = 0.… |
1 mg |
25600-1 |
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TC 2559 (fumarate) |
A partial agonist for α4β2 subunit-containing nAChRs (EC50 = 0.… |
10 mg |
25600-10 |
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TC 2559 (fumarate) |
A partial agonist for α4β2 subunit-containing nAChRs (EC50 = 0.… |
25 mg |
25600-25 |
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TC 2559 (fumarate) |
A partial agonist for α4β2 subunit-containing nAChRs (EC50 = 0.… |
5 mg |
25600-5 |
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TCH-165 |
A proteasome assembly modulator; selectively activates the chymotrypsin-li… |
10 mg |
40454-10 |
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TCH-165 |
A proteasome assembly modulator; selectively activates the chymotrypsin-li… |
25 mg |
40454-25 |
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TCH-165 |
A proteasome assembly modulator; selectively activates the chymotrypsin-li… |
5 mg |
40454-5 |
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TC HSD 21 |
A 17β-HSD3 inhibitor (IC50 = 14 nM in HeLa cells expressing the recom… |
1 mg |
29730-1 |
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TC HSD 21 |
A 17β-HSD3 inhibitor (IC50 = 14 nM in HeLa cells expressing the recom… |
5 mg |
29730-5 |
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TC 14012 (hydrochloride) |
A CXCR4 antagonist (IC50 = 2.9 nM) and CXCR7 agonist; induces β-arres… |
1 mg |
38140-1 |
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TC 14012 (hydrochloride) |
A CXCR4 antagonist (IC50 = 2.9 nM) and CXCR7 agonist; induces β-arres… |
5 mg |
38140-5 |
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TC 14012 (hydrochloride) |
A CXCR4 antagonist (IC50 = 2.9 nM) and CXCR7 agonist; induces β-arres… |
500 µg |
38140-500 |
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TC-I 2000 |
A TRPM8 antagonist (IC50 = 53 nM) |
10 mg |
35463-10 |
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TC-I 2000 |
A TRPM8 antagonist (IC50 = 53 nM) |
25 mg |
35463-25 |
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TC-I 2000 |
A TRPM8 antagonist (IC50 = 53 nM) |
5 mg |
35463-5 |
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TC-I 2000 |
A TRPM8 antagonist (IC50 = 53 nM) |
50 mg |
35463-50 |
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TCID |
A tetrachloro indandione that acts as a potent inhibitor of UCH-L3 and dem… |
10 mg |
16353-10 |
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TCID |
A tetrachloro indandione that acts as a potent inhibitor of UCH-L3 and dem… |
25 mg |
16353-25 |
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TCID |
A tetrachloro indandione that acts as a potent inhibitor of UCH-L3 and dem… |
5 mg |
16353-5 |
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TCL053 |
An ionizable cationic amino lipid; has been used in the generation of LNPs… |
10 mg |
37045-10 |
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TCL053 |
An ionizable cationic amino lipid; has been used in the generation of LNPs… |
25 mg |
37045-25 |
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TCL053 |
An ionizable cationic amino lipid; has been used in the generation of LNPs… |
5 mg |
37045-5 |
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TCL053 |
An ionizable cationic amino lipid; has been used in the generation of LNPs… |
50 mg |
37045-50 |
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TC LPA5 4 |
An LPA5 antagonist (IC50 = 0.8 µM in McA-RH7777 cells expressing the… |
1 mg |
17719-1 |
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TC LPA5 4 |
An LPA5 antagonist (IC50 = 0.8 µM in McA-RH7777 cells expressing the… |
10 mg |
17719-10 |
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TC LPA5 4 |
An LPA5 antagonist (IC50 = 0.8 µM in McA-RH7777 cells expressing the… |
5 mg |
17719-5 |
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TC LPA5 4 |
An LPA5 antagonist (IC50 = 0.8 µM in McA-RH7777 cells expressing the… |
50 mg |
17719-50 |
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TCN 201 |
A selective antagonist of NMDA receptors containing the NR2A subunit (pIC5… |
1 mg |
19086-1 |
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TCN 201 |
A selective antagonist of NMDA receptors containing the NR2A subunit (pIC5… |
10 mg |
19086-10 |
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TCN 201 |
A selective antagonist of NMDA receptors containing the NR2A subunit (pIC5… |
5 mg |
19086-5 |
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TCN 238 |
An orally bioavailable positive allosteric modulator of mGluR4 (EC50 = 1 &… |
10 mg |
11994-10 |
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TCN 238 |
An orally bioavailable positive allosteric modulator of mGluR4 (EC50 = 1 &… |
25 mg |
11994-25 |
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TCN 238 |
An orally bioavailable positive allosteric modulator of mGluR4 (EC50 = 1 &… |
5 mg |
11994-5 |
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TC-O 9311 |
An agonist of GPR139 (EC50 = 39 nM in a calcium mobilization assay); selec… |
1 mg |
14030-1 |
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TC-O 9311 |
An agonist of GPR139 (EC50 = 39 nM in a calcium mobilization assay); selec… |
10 mg |
14030-10 |
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TC-O 9311 |
An agonist of GPR139 (EC50 = 39 nM in a calcium mobilization assay); selec… |
25 mg |
14030-25 |
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TC-O 9311 |
An agonist of GPR139 (EC50 = 39 nM in a calcium mobilization assay); selec… |
5 mg |
14030-5 |
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TCPOBOP |
An agonist for mCAR (EC50 = 20 nM) that is effective for the mouse recepto… |
10 mg |
14140-10 |
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TCPOBOP |
An agonist for mCAR (EC50 = 20 nM) that is effective for the mouse recepto… |
25 mg |
14140-25 |
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TCPOBOP |
An agonist for mCAR (EC50 = 20 nM) that is effective for the mouse recepto… |
5 mg |
14140-5 |
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TCPOBOP |
An agonist for mCAR (EC50 = 20 nM) that is effective for the mouse recepto… |
50 mg |
14140-50 |
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TCPTP (human, recombinant; aa 1-314) |
Source: Recombinant human N-terminal His-GST-tagged TCPTP expressed in ins… |
100 µg |
32021-100 |
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TCS 1102 |
A dual antagonist of both OX1R and OX2R (Kis = 0.2 and 3 nM, respectively)… |
1 mg |
18495-1 |
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