CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 847 of 865
Non-Antibody Products
Page 847 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| WAY-169916 | A pathway-selective estrogen receptor ligand; binds to human ERα and… | 50 mg | 35842-50 | More Info |
| WAY-200070 | A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… | 10 mg | 23323-10 | More Info |
| WAY-200070 | A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… | 25 mg | 23323-25 | More Info |
| WAY-200070 | A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… | 5 mg | 23323-5 | More Info |
| WAY-200070 | A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… | 50 mg | 23323-50 | More Info |
| WAY-262611 | An inhibitor of Dkk1 that activates the Wnt signaling pathway, stimulating… | 1 mg | 17704-1 | More Info |
| WAY-262611 | An inhibitor of Dkk1 that activates the Wnt signaling pathway, stimulating… | 10 mg | 17704-10 | More Info |
| WAY-262611 | An inhibitor of Dkk1 that activates the Wnt signaling pathway, stimulating… | 25 mg | 17704-25 | More Info |
| WAY-262611 | An inhibitor of Dkk1 that activates the Wnt signaling pathway, stimulating… | 5 mg | 17704-5 | More Info |
| WAY-316606 | An sFRP1 inhibitor (IC50 = 0.5 µM); increases Wnt signaling in U2OS… | 1 mg | 26324-1 | More Info |
| WAY-316606 | An sFRP1 inhibitor (IC50 = 0.5 µM); increases Wnt signaling in U2OS… | 10 mg | 26324-10 | More Info |
| WAY-316606 | An sFRP1 inhibitor (IC50 = 0.5 µM); increases Wnt signaling in U2OS… | 5 mg | 26324-5 | More Info |
| WAY-600 | An mTOR inhibitor (IC50 = 0.009 µM); selectively inhibits mTOR over… | 1 mg | 29214-1 | More Info |
| WAY-600 | An mTOR inhibitor (IC50 = 0.009 µM); selectively inhibits mTOR over… | 10 mg | 29214-10 | More Info |
| WAY-600 | An mTOR inhibitor (IC50 = 0.009 µM); selectively inhibits mTOR over… | 5 mg | 29214-5 | More Info |
| WAY-208466 (hydrochloride) | A selective 5-HT6 receptor agonist (EC50 = 7.3 nM at the human 5-HT6 recep… | 1 mg | 11938-1 | More Info |
| WAY-208466 (hydrochloride) | A selective 5-HT6 receptor agonist (EC50 = 7.3 nM at the human 5-HT6 recep… | 10 mg | 11938-10 | More Info |
| WAY-208466 (hydrochloride) | A selective 5-HT6 receptor agonist (EC50 = 7.3 nM at the human 5-HT6 recep… | 25 mg | 11938-25 | More Info |
| WAY-208466 (hydrochloride) | A selective 5-HT6 receptor agonist (EC50 = 7.3 nM at the human 5-HT6 recep… | 5 mg | 11938-5 | More Info |
| WAY-100635 (maleate) | A potent, silent antagonist of serotonin 5-HT1A receptors (IC50 = 2.2 nM;… | 10 mg | 14599-10 | More Info |
| WAY-100635 (maleate) | A potent, silent antagonist of serotonin 5-HT1A receptors (IC50 = 2.2 nM;… | 5 mg | 14599-5 | More Info |
| WAY-100635 (maleate) | A potent, silent antagonist of serotonin 5-HT1A receptors (IC50 = 2.2 nM;… | 50 mg | 14599-50 | More Info |
| WB 4101 (hydrochloride) | An α-AR antagonist; inhibits norepinephrine-induced contraction in i… | 100 mg | 29528-100 | More Info |
| WB 4101 (hydrochloride) | An α-AR antagonist; inhibits norepinephrine-induced contraction in i… | 250 mg | 29528-250 | More Info |
| WB 4101 (hydrochloride) | An α-AR antagonist; inhibits norepinephrine-induced contraction in i… | 50 mg | 29528-50 | More Info |
| WDR5-0103 | A small molecule that binds a peptide-binding pocket on WDR5 (Kd = 450 nM)… | 1 mg | 13945-1 | More Info |
| WDR5-0103 | A small molecule that binds a peptide-binding pocket on WDR5 (Kd = 450 nM)… | 10 mg | 13945-10 | More Info |
| WDR5-0103 | A small molecule that binds a peptide-binding pocket on WDR5 (Kd = 450 nM)… | 25 mg | 13945-25 | More Info |
| WDR5-0103 | A small molecule that binds a peptide-binding pocket on WDR5 (Kd = 450 nM)… | 5 mg | 13945-5 | More Info |
| WDR5 (human, recombinant) | Source: Recombinant protein expressed in E. coli • WDR5 has been demo… | 100 µg | 10944-100 | More Info |
| WDR5-MYC Probe 12 | An inhibitor of the Myc-WDR5 protein-protein interaction (IC50 = 0.39 &mic… | 1 mg | 39304-1 | More Info |
| WDR5-MYC Probe 12 | An inhibitor of the Myc-WDR5 protein-protein interaction (IC50 = 0.39 &mic… | 10 mg | 39304-10 | More Info |
| WDR5-MYC Probe 12 | An inhibitor of the Myc-WDR5 protein-protein interaction (IC50 = 0.39 &mic… | 5 mg | 39304-5 | More Info |
| Wedelolactone | A natural coumestan that inhibits NF-κB signaling at the level of IK… | 1 mg | 11796-1 | More Info |
| Wedelolactone | A natural coumestan that inhibits NF-κB signaling at the level of IK… | 5 mg | 11796-5 | More Info |
| Wedelolactone | A natural coumestan that inhibits NF-κB signaling at the level of IK… | 500 µg | 11796-500 | More Info |
| Wee1 Inhibitor | An inhibitor of Wee1 (IC50 = 11 nM); selective for Wee1 over Chk1 (IC50 =… | 1 mg | 35391-1 | More Info |
| WEHI-345 | An inhibitor of RIPK2 (IC50 = 130 nM in a kinase assay using human recombi… | 1 mg | 23023-1 | More Info |
| WEHI-345 | An inhibitor of RIPK2 (IC50 = 130 nM in a kinase assay using human recombi… | 10 mg | 23023-10 | More Info |
| WEHI-345 | An inhibitor of RIPK2 (IC50 = 130 nM in a kinase assay using human recombi… | 25 mg | 23023-25 | More Info |
| WEHI-345 | An inhibitor of RIPK2 (IC50 = 130 nM in a kinase assay using human recombi… | 5 mg | 23023-5 | More Info |
| WEHI-539 | A selective inhibitor of Bcl-xL (IC50 = 1.1 nM); induces apoptosis specifi… | 1 mg | 21478-1 | More Info |
| WEHI-539 | A selective inhibitor of Bcl-xL (IC50 = 1.1 nM); induces apoptosis specifi… | 10 mg | 21478-10 | More Info |
| WEHI-539 | A selective inhibitor of Bcl-xL (IC50 = 1.1 nM); induces apoptosis specifi… | 5 mg | 21478-5 | More Info |
| 96-Well Solid Plate (white) | n/a | 1 ea | 700029-1 | More Info |
| WF-3681 | A fungal metabolite; inhibits aldose reductase (IC50 = 0.25 µM) | 100 µg | 33523-100 | More Info |
| WF-3681 | A fungal metabolite; inhibits aldose reductase (IC50 = 0.25 µM) | 500 µg | 33523-500 | More Info |
| WH-4-023 | A selective inhibitor of the Src family of non-receptor tyrosine kinases (… | 1 mg | 9002067-1 | More Info |
| WH-4-023 | A selective inhibitor of the Src family of non-receptor tyrosine kinases (… | 10 mg | 9002067-10 | More Info |
| WH-4-023 | A selective inhibitor of the Src family of non-receptor tyrosine kinases (… | 25 mg | 9002067-25 | More Info |
| WH-4-023 | A selective inhibitor of the Src family of non-receptor tyrosine kinases (… | 5 mg | 9002067-5 | More Info |
| WHI-P131 | A selective inhibitor of JAK3 with an IC50 value of 78 µM that does… | 1 mg | 10011246-1 | More Info |
| WHI-P131 | A selective inhibitor of JAK3 with an IC50 value of 78 µM that does… | 10 mg | 10011246-10 | More Info |
| WHI-P131 | A selective inhibitor of JAK3 with an IC50 value of 78 µM that does… | 25 mg | 10011246-25 | More Info |
| WHI-P131 | A selective inhibitor of JAK3 with an IC50 value of 78 µM that does… | 5 mg | 10011246-5 | More Info |
| WHI-P154 | A quinazoline derivative that exhibits immunosuppressive effects by select… | 10 mg | 16178-10 | More Info |
| WHI-P154 | A quinazoline derivative that exhibits immunosuppressive effects by select… | 25 mg | 16178-25 | More Info |
| WHI-P154 | A quinazoline derivative that exhibits immunosuppressive effects by select… | 5 mg | 16178-5 | More Info |
| WHI-P180 | A multi-kinase inhibitor (IC50s = 4.5 and 66 nM for human recombinant RET… | 1 mg | 23452-1 | More Info |
| WHI-P180 | A multi-kinase inhibitor (IC50s = 4.5 and 66 nM for human recombinant RET… | 5 mg | 23452-5 | More Info |
| WHI-P180 | A multi-kinase inhibitor (IC50s = 4.5 and 66 nM for human recombinant RET… | 500 µg | 23452-500 | More Info |
| WHI-P258 | A negative control for JAK3 inhibition; molecular modeling estimated a Ki… | 10 mg | 23453-10 | More Info |
| WHI-P258 | A negative control for JAK3 inhibition; molecular modeling estimated a Ki… | 25 mg | 23453-25 | More Info |
| WHI-P258 | A negative control for JAK3 inhibition; molecular modeling estimated a Ki… | 5 mg | 23453-5 | More Info |
| WHI-P97 | A JAK3 inhibitor (IC50 = 11 µM); inhibits FcεRI-mediated LTC… | 1 mg | 36385-1 | More Info |
| WHI-P97 | A JAK3 inhibitor (IC50 = 11 µM); inhibits FcεRI-mediated LTC… | 10 mg | 36385-10 | More Info |
| WHI-P97 | A JAK3 inhibitor (IC50 = 11 µM); inhibits FcεRI-mediated LTC… | 25 mg | 36385-25 | More Info |
| WHI-P97 | A JAK3 inhibitor (IC50 = 11 µM); inhibits FcεRI-mediated LTC… | 5 mg | 36385-5 | More Info |
| 1400W (hydrochloride) | 1400W is a potent, selective inhibitor of iNOS.{4277} Using purified human… | 10 mg | 81520-10 | More Info |
| 1400W (hydrochloride) | 1400W is a potent, selective inhibitor of iNOS.{4277} Using purified human… | 100 mg | 81520-100 | More Info |
| 1400W (hydrochloride) | 1400W is a potent, selective inhibitor of iNOS.{4277} Using purified human… | 5 mg | 81520-5 | More Info |
| 1400W (hydrochloride) | 1400W is a potent, selective inhibitor of iNOS.{4277} Using purified human… | 50 mg | 81520-50 | More Info |
| W-13 (hydrochloride) | A potent antagonist of calmodulin (IC50 = 22 µM) that is widely used… | 1 mg | 14277-1 | More Info |
| W-13 (hydrochloride) | A potent antagonist of calmodulin (IC50 = 22 µM) that is widely used… | 10 mg | 14277-10 | More Info |
| W-13 (hydrochloride) | A potent antagonist of calmodulin (IC50 = 22 µM) that is widely used… | 5 mg | 14277-5 | 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
Sales: sales@caymanchem.com
http://www.caymanchem.com
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