CBL-018 |
An analog of JWH 018 where the core indole base and the naphthalene group… |
10 mg |
16443-10 |
More Info
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CBL-018 |
An analog of JWH 018 where the core indole base and the naphthalene group… |
5 mg |
16443-5 |
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CBL0137 (hydrochloride) |
A water soluble and metabolically stable curaxin that activates p53 with a… |
1 mg |
19373-1 |
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CBL0137 (hydrochloride) |
A water soluble and metabolically stable curaxin that activates p53 with a… |
10 mg |
19373-10 |
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CBL0137 (hydrochloride) |
A water soluble and metabolically stable curaxin that activates p53 with a… |
5 mg |
19373-5 |
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CBNQ |
An analytical reference standard categorized as an oxidative product of ca… |
1 mg |
30863-1 |
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CBNQ |
An analytical reference standard categorized as an oxidative product of ca… |
5 mg |
30863-5 |
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C11 BODIPY 581/591 |
A lipid-soluble ratiometric fluorescent indicator of lipid oxidation; ex /… |
1 mg |
27086-1 |
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C3 BODIPY Ganglioside GM1 (d18:1/3:0) (ammonium salt) |
A fluorescently labeled form of ganglioside GM1; ex / em = 503 / 512 nm, r… |
100 µg |
33799-100 |
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13C28-Bongkrekic Acid |
An internal standard for the quantification of bongkrekic acid by GC- or L… |
1.2 mL |
39454-12 |
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CBP bromodomain TR-FRET Assay Kit |
Cayman's CBP bromodomain TR-FRET Assay Kit is a homogeneous, time-resolved… |
1920 Well |
600850-1920WELLS |
More Info
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CBP bromodomain TR-FRET Assay Kit |
Cayman's CBP bromodomain TR-FRET Assay Kit is a homogeneous, time-resolved… |
384 Well |
600850-384WELLS |
More Info
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CBP bromodomain TR-FRET Assay Kit |
Cayman's CBP bromodomain TR-FRET Assay Kit is a homogeneous, time-resolved… |
9600 Well |
600850-9600WELLS |
More Info
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CBR-5884 |
An inhibitor of PHGDH, inhibiting serine synthesis from 3-PG in cells (IC5… |
1 mg |
19236-1 |
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CBR-5884 |
An inhibitor of PHGDH, inhibiting serine synthesis from 3-PG in cells (IC5… |
10 mg |
19236-10 |
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CBR-5884 |
An inhibitor of PHGDH, inhibiting serine synthesis from 3-PG in cells (IC5… |
25 mg |
19236-25 |
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CBR-5884 |
An inhibitor of PHGDH, inhibiting serine synthesis from 3-PG in cells (IC5… |
5 mg |
19236-5 |
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CB1 Receptor Blocking Peptide |
Peptide Sequence: human, rat, and mouse CB1 receptor sequence amino acids… |
200 µg |
301500-200 |
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CB2 Receptor Blocking Peptide |
Peptide Sequence: human CB2 receptor sequence amino acids 20-33 (NPMKDYMIL… |
200 µg |
301550-200 |
More Info
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CB1 Receptor (C-Term) Blocking Peptide |
Peptide Sequence: CB1 receptor (C-Term) amino acids 461-472 · To be… |
1 ea |
10006591-1 |
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CBX2 chromodomain (human recombinant) |
Source: Recombinant N-terminal GST-tagged protein expressed in E. coli &bu… |
100 µg |
14769-100 |
More Info
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CBX1 (human recombinant) |
Source: Recombinant N-terminal GST-tagged protein expressed in E. coli &bu… |
100 µg |
14768-100 |
More Info
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CBX3 (human recombinant) |
Source: Recombinant N-terminal GST-tagged protein expressed in E. coli &bu… |
100 µg |
15467-100 |
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CBX5 (human recombinant) |
Source: Recombinant N-terminal His-tagged protein expressed in E. coli &bu… |
100 µg |
11235-100 |
More Info
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CC-115 |
A dual inhibitor of mTOR and DNA-PK (IC50s = 0.021 and 0.013 µM, res… |
1 mg |
19420-1 |
More Info
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CC-115 |
A dual inhibitor of mTOR and DNA-PK (IC50s = 0.021 and 0.013 µM, res… |
10 mg |
19420-10 |
More Info
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CC-115 |
A dual inhibitor of mTOR and DNA-PK (IC50s = 0.021 and 0.013 µM, res… |
25 mg |
19420-25 |
More Info
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CC-115 |
A dual inhibitor of mTOR and DNA-PK (IC50s = 0.021 and 0.013 µM, res… |
5 mg |
19420-5 |
More Info
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CC-122 |
A pleiotropic pathway modifier with anticancer activity; binds to cereblon… |
1 mg |
26257-1 |
More Info
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CC-122 |
A pleiotropic pathway modifier with anticancer activity; binds to cereblon… |
10 mg |
26257-10 |
More Info
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CC-122 |
A pleiotropic pathway modifier with anticancer activity; binds to cereblon… |
25 mg |
26257-25 |
More Info
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CC-122 |
A pleiotropic pathway modifier with anticancer activity; binds to cereblon… |
5 mg |
26257-5 |
More Info
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CC-223 |
A potent, selective inhibitor of mTOR (IC50 = 16 nM); inhibits growth and… |
1 mg |
19917-1 |
More Info
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CC-223 |
A potent, selective inhibitor of mTOR (IC50 = 16 nM); inhibits growth and… |
10 mg |
19917-10 |
More Info
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CC-223 |
A potent, selective inhibitor of mTOR (IC50 = 16 nM); inhibits growth and… |
25 mg |
19917-25 |
More Info
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CC-223 |
A potent, selective inhibitor of mTOR (IC50 = 16 nM); inhibits growth and… |
5 mg |
19917-5 |
More Info
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CC-401 |
A potent, selective inhibitor of all three JNK isoforms (Ki values range f… |
1 mg |
18867-1 |
More Info
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CC-401 |
A potent, selective inhibitor of all three JNK isoforms (Ki values range f… |
10 mg |
18867-10 |
More Info
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CC-401 |
A potent, selective inhibitor of all three JNK isoforms (Ki values range f… |
5 mg |
18867-5 |
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CC-671 |
A dual inhibitor of Mps1 / TTK and Clk2 (IC50s = 5 and 3 nM, respectively)… |
1 mg |
26184-1 |
More Info
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CC-671 |
A dual inhibitor of Mps1 / TTK and Clk2 (IC50s = 5 and 3 nM, respectively)… |
10 mg |
26184-10 |
More Info
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CC-671 |
A dual inhibitor of Mps1 / TTK and Clk2 (IC50s = 5 and 3 nM, respectively)… |
5 mg |
26184-5 |
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CC-885 |
A cereblon modulator; has an antiproliferative effect on human myeloid leu… |
1 mg |
19966-1 |
More Info
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CC-885 |
A cereblon modulator; has an antiproliferative effect on human myeloid leu… |
10 mg |
19966-10 |
More Info
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CC-885 |
A cereblon modulator; has an antiproliferative effect on human myeloid leu… |
5 mg |
19966-5 |
More Info
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CC-885 |
A cereblon modulator; has an antiproliferative effect on human myeloid leu… |
500 µg |
19966-500 |
More Info
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CC-90009 |
A modulator of cereblon; binds to cereblon and enhances the protein-protei… |
1 mg |
33692-1 |
More Info
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CC-90009 |
A modulator of cereblon; binds to cereblon and enhances the protein-protei… |
10 mg |
33692-10 |
More Info
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CC-90009 |
A modulator of cereblon; binds to cereblon and enhances the protein-protei… |
25 mg |
33692-25 |
More Info
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CC-90009 |
A modulator of cereblon; binds to cereblon and enhances the protein-protei… |
5 mg |
33692-5 |
More Info
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