(R)-Norketamine (hydrochloride) |
An analytical reference standard categorized as an arylcyclohexylamine; an… |
5 mg |
37821-5 |
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Ro 01-6128 |
A positive allosteric modulator of mGluR1; potentiates glutamate-induced c… |
1 mg |
11991-1 |
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Ro 01-6128 |
A positive allosteric modulator of mGluR1; potentiates glutamate-induced c… |
10 mg |
11991-10 |
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Ro 01-6128 |
A positive allosteric modulator of mGluR1; potentiates glutamate-induced c… |
5 mg |
11991-5 |
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Ro 0335 |
An NNRTI and active metabolite of elsulfavirine; inhibits HIV-1 reverse tr… |
10 mg |
36124-10 |
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Ro 0335 |
An NNRTI and active metabolite of elsulfavirine; inhibits HIV-1 reverse tr… |
100 mg |
36124-100 |
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Ro 0335 |
An NNRTI and active metabolite of elsulfavirine; inhibits HIV-1 reverse tr… |
5 mg |
36124-5 |
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Ro 0335 |
An NNRTI and active metabolite of elsulfavirine; inhibits HIV-1 reverse tr… |
50 mg |
36124-50 |
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Ro 08-2750 |
A p75NTR ligand; completely inhibits NGF binding to p75NTR in PC12 cells a… |
1 mg |
28772-1 |
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Ro 08-2750 |
A p75NTR ligand; completely inhibits NGF binding to p75NTR in PC12 cells a… |
10 mg |
28772-10 |
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Ro 08-2750 |
A p75NTR ligand; completely inhibits NGF binding to p75NTR in PC12 cells a… |
5 mg |
28772-5 |
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Ro 106-9920 |
A small molecule inhibitor of NF-κB-dependent expression of TNF-&alp… |
1 mg |
15373-1 |
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Ro 106-9920 |
A small molecule inhibitor of NF-κB-dependent expression of TNF-&alp… |
10 mg |
15373-10 |
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Ro 106-9920 |
A small molecule inhibitor of NF-κB-dependent expression of TNF-&alp… |
5 mg |
15373-5 |
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Ro 20-1724 |
A cell-permeable, selective PDE4 inhibitor (IC50 = 2 µM); inhibits t… |
100 mg |
18272-100 |
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Ro 20-1724 |
A cell-permeable, selective PDE4 inhibitor (IC50 = 2 µM); inhibits t… |
25 mg |
18272-25 |
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Ro 20-1724 |
A cell-permeable, selective PDE4 inhibitor (IC50 = 2 µM); inhibits t… |
50 mg |
18272-50 |
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Ro 3280 |
A selective Plk1 inhibitor (IC50s = 3 and 6 nM in an enzymatic assay and H… |
1 mg |
21669-1 |
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Ro 3280 |
A selective Plk1 inhibitor (IC50s = 3 and 6 nM in an enzymatic assay and H… |
10 mg |
21669-10 |
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Ro 3280 |
A selective Plk1 inhibitor (IC50s = 3 and 6 nM in an enzymatic assay and H… |
25 mg |
21669-25 |
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Ro 3280 |
A selective Plk1 inhibitor (IC50s = 3 and 6 nM in an enzymatic assay and H… |
5 mg |
21669-5 |
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Ro 3306 |
A cell-permeable, reversible inhibitor of Cdk1, showing preference for Cdk… |
1 mg |
15149-1 |
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Ro 3306 |
A cell-permeable, reversible inhibitor of Cdk1, showing preference for Cdk… |
10 mg |
15149-10 |
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Ro 3306 |
A cell-permeable, reversible inhibitor of Cdk1, showing preference for Cdk… |
5 mg |
15149-5 |
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Ro 3306 |
A cell-permeable, reversible inhibitor of Cdk1, showing preference for Cdk… |
50 mg |
15149-50 |
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Ro 41-0960 |
A COMT inhibitor; prevents L-DOPA-induced dopaminergic neuron loss in prim… |
10 mg |
29621-10 |
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Ro 41-0960 |
A COMT inhibitor; prevents L-DOPA-induced dopaminergic neuron loss in prim… |
25 mg |
29621-25 |
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Ro 41-0960 |
A COMT inhibitor; prevents L-DOPA-induced dopaminergic neuron loss in prim… |
5 mg |
29621-5 |
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Ro 48-8071 |
An oxidosqualene cyclase inhibitor with cholesterol lowering activity; inh… |
10 mg |
10006415-10 |
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Ro 48-8071 |
An oxidosqualene cyclase inhibitor with cholesterol lowering activity; inh… |
100 mg |
10006415-100 |
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Ro 48-8071 |
An oxidosqualene cyclase inhibitor with cholesterol lowering activity; inh… |
5 mg |
10006415-5 |
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Ro 48-8071 |
An oxidosqualene cyclase inhibitor with cholesterol lowering activity; inh… |
50 mg |
10006415-50 |
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Ro 4929097 |
A potent, selective inhibitor of γ-secretase (IC50 = 4 nM) that bloc… |
1 mg |
19996-1 |
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Ro 4929097 |
A potent, selective inhibitor of γ-secretase (IC50 = 4 nM) that bloc… |
10 mg |
19996-10 |
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Ro 4929097 |
A potent, selective inhibitor of γ-secretase (IC50 = 4 nM) that bloc… |
5 mg |
19996-5 |
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Ro 4929097 |
A potent, selective inhibitor of γ-secretase (IC50 = 4 nM) that bloc… |
500 µg |
19996-500 |
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Ro 5126766 |
A dual inhibitor of MEK1 (IC50 = 160 nM) and Raf kinases (IC50s = 56, 19,… |
1 mg |
29197-1 |
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Ro 5126766 |
A dual inhibitor of MEK1 (IC50 = 160 nM) and Raf kinases (IC50s = 56, 19,… |
5 mg |
29197-5 |
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Ro 60-0175 |
A 5-HT2 agonist; stimulates increases in intracellular calcium levels in C… |
1 mg |
29520-1 |
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Ro 60-0175 |
A 5-HT2 agonist; stimulates increases in intracellular calcium levels in C… |
5 mg |
29520-5 |
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Ro 61-8048 |
A potent inhibitor of kynurenine 3-hydroxylase (IC50 = 37 nM), preventing… |
10 mg |
15199-10 |
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Ro 61-8048 |
A potent inhibitor of kynurenine 3-hydroxylase (IC50 = 37 nM), preventing… |
25 mg |
15199-25 |
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Ro 61-8048 |
A potent inhibitor of kynurenine 3-hydroxylase (IC50 = 37 nM), preventing… |
5 mg |
15199-5 |
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Ro 61-8048 |
A potent inhibitor of kynurenine 3-hydroxylase (IC50 = 37 nM), preventing… |
50 mg |
15199-50 |
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Ro 67-4853 |
A selective, positive allosteric modulator of mGluR1, enhancing glutamate-… |
1 mg |
11992-1 |
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Ro 67-4853 |
A selective, positive allosteric modulator of mGluR1, enhancing glutamate-… |
10 mg |
11992-10 |
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Ro 67-4853 |
A selective, positive allosteric modulator of mGluR1, enhancing glutamate-… |
5 mg |
11992-5 |
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Ro 67-7476 |
A positive allosteric modulator of mGluR1; enhances glutamate-induced calc… |
1 mg |
11993-1 |
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Ro 67-7476 |
A positive allosteric modulator of mGluR1; enhances glutamate-induced calc… |
10 mg |
11993-10 |
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Ro 67-7476 |
A positive allosteric modulator of mGluR1; enhances glutamate-induced calc… |
25 mg |
11993-25 |
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