CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 787 of 870
Non-Antibody Products
Page 787 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| TAK-960 | A selective inhibitor of Plks (IC50s = 0.8, 16.9, and 50.2 nM for Plk1, Pl… | 1 mg | 17701-1 | More Info |
| TAK-960 | A selective inhibitor of Plks (IC50s = 0.8, 16.9, and 50.2 nM for Plk1, Pl… | 10 mg | 17701-10 | More Info |
| TAK-960 | A selective inhibitor of Plks (IC50s = 0.8, 16.9, and 50.2 nM for Plk1, Pl… | 5 mg | 17701-5 | More Info |
| TAK-960 | A selective inhibitor of Plks (IC50s = 0.8, 16.9, and 50.2 nM for Plk1, Pl… | 50 mg | 17701-50 | More Info |
| TAK-981 | An inhibitor of SAE (IC50 = in vitro; decreases intratumor levels of SUMOl… | 1 mg | 32741-1 | More Info |
| TAK-981 | An inhibitor of SAE (IC50 = in vitro; decreases intratumor levels of SUMOl… | 10 mg | 32741-10 | More Info |
| TAK-981 | An inhibitor of SAE (IC50 = in vitro; decreases intratumor levels of SUMOl… | 25 mg | 32741-25 | More Info |
| TAK-981 | An inhibitor of SAE (IC50 = in vitro; decreases intratumor levels of SUMOl… | 5 mg | 32741-5 | More Info |
| Takeda-6d | A dual inhibitor of RAF kinases and VEGFR2; inhibits wild-type B-RAF, muta… | 1 mg | 35754-1 | More Info |
| Takeda-6d | A dual inhibitor of RAF kinases and VEGFR2; inhibits wild-type B-RAF, muta… | 5 mg | 35754-5 | More Info |
| Takinib | A TAK1 inhibitor (IC50 = 9.5 nM); selective for TAK1 over IRAK1, IRAK4, GC… | 1 mg | 24161-1 | More Info |
| Takinib | A TAK1 inhibitor (IC50 = 9.5 nM); selective for TAK1 over IRAK1, IRAK4, GC… | 10 mg | 24161-10 | More Info |
| Takinib | A TAK1 inhibitor (IC50 = 9.5 nM); selective for TAK1 over IRAK1, IRAK4, GC… | 25 mg | 24161-25 | More Info |
| Takinib | A TAK1 inhibitor (IC50 = 9.5 nM); selective for TAK1 over IRAK1, IRAK4, GC… | 5 mg | 24161-5 | More Info |
| TAK1-TAB1 Fusion (human, recombinant) | Source: Active recombinant N-terminal GST-tagged human TAK1 fused to TAB1… | 10 µg | 33990-10 | More Info |
| Talabostat (mesylate) | A non-selective inhibitor of DPPs (IC50s = >4, 310, 4, 11, 560, and 390 nM… | 10 mg | 29007-10 | More Info |
| Talabostat (mesylate) | A non-selective inhibitor of DPPs (IC50s = >4, 310, 4, 11, 560, and 390 nM… | 25 mg | 29007-25 | More Info |
| Talabostat (mesylate) | A non-selective inhibitor of DPPs (IC50s = >4, 310, 4, 11, 560, and 390 nM… | 5 mg | 29007-5 | More Info |
| Talabostat (mesylate) | A non-selective inhibitor of DPPs (IC50s = >4, 310, 4, 11, 560, and 390 nM… | 50 mg | 29007-50 | More Info |
| Talampanel | An allosteric AMPA receptor antagonist (IC50 = 2.5 µM); reduces the… | 10 mg | 15341-10 | More Info |
| Talampanel | An allosteric AMPA receptor antagonist (IC50 = 2.5 µM); reduces the… | 25 mg | 15341-25 | More Info |
| Talampanel | An allosteric AMPA receptor antagonist (IC50 = 2.5 µM); reduces the… | 5 mg | 15341-5 | More Info |
| Talampanel | An allosteric AMPA receptor antagonist (IC50 = 2.5 µM); reduces the… | 50 mg | 15341-50 | More Info |
| Talaporfin (sodium salt) | A photosensitizer; induces apoptosis, DNA DSBs, and the production of ROS… | 10 mg | 35722-10 | More Info |
| Talaporfin (sodium salt) | A photosensitizer; induces apoptosis, DNA DSBs, and the production of ROS… | 25 mg | 35722-25 | More Info |
| Talaporfin (sodium salt) | A photosensitizer; induces apoptosis, DNA DSBs, and the production of ROS… | 5 mg | 35722-5 | More Info |
| Talaporfin (sodium salt) | A photosensitizer; induces apoptosis, DNA DSBs, and the production of ROS… | 50 mg | 35722-50 | More Info |
| Talaromycesone A | A fungal metabolite; active against S. epidermidis and MRSA (IC50s = 3.70… | 1 mg | 32932-1 | More Info |
| Talaromycesone A | A fungal metabolite; active against S. epidermidis and MRSA (IC50s = 3.70… | 5 mg | 32932-5 | More Info |
| Talatisamine | A diterpene alkaloid with diverse biological activities; blocks IK current… | 10 mg | 27721-10 | More Info |
| Talatisamine | A diterpene alkaloid with diverse biological activities; blocks IK current… | 25 mg | 27721-25 | More Info |
| Talatisamine | A diterpene alkaloid with diverse biological activities; blocks IK current… | 5 mg | 27721-5 | More Info |
| Talatisamine | A diterpene alkaloid with diverse biological activities; blocks IK current… | 50 mg | 27721-50 | More Info |
| Taleranol | A β-resorcylic acid lactone; induces synthesis of the uterine protein… | 1 mg | 28299-1 | More Info |
| Taleranol | A β-resorcylic acid lactone; induces synthesis of the uterine protein… | 10 mg | 28299-10 | More Info |
| Taleranol | A β-resorcylic acid lactone; induces synthesis of the uterine protein… | 25 mg | 28299-25 | More Info |
| Taleranol | A β-resorcylic acid lactone; induces synthesis of the uterine protein… | 5 mg | 28299-5 | More Info |
| Talnetant | A nonpeptide NK3 antagonist (Ki = 1 nM); selective for NK3 over NK1 and NK… | 100 mg | 29699-100 | More Info |
| Talnetant | A nonpeptide NK3 antagonist (Ki = 1 nM); selective for NK3 over NK1 and NK… | 250 mg | 29699-250 | More Info |
| Talnetant | A nonpeptide NK3 antagonist (Ki = 1 nM); selective for NK3 over NK1 and NK… | 500 mg | 29699-500 | More Info |
| Talniflumate | A prodrug form of niflumic acid; decreases the rate of chloride / bicarbon… | 10 mg | 29623-10 | More Info |
| Talniflumate | A prodrug form of niflumic acid; decreases the rate of chloride / bicarbon… | 25 mg | 29623-25 | More Info |
| Talniflumate | A prodrug form of niflumic acid; decreases the rate of chloride / bicarbon… | 5 mg | 29623-5 | More Info |
| Talniflumate | A prodrug form of niflumic acid; decreases the rate of chloride / bicarbon… | 50 mg | 29623-50 | More Info |
| Tamoxifen | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 1 g | 13258-1 | More Info |
| Tamoxifen | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 10 g | 13258-10 | More Info |
| Tamoxifen | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 5 g | 13258-5 | More Info |
| Tamoxifen | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 500 mg | 13258-500 | More Info |
| Tamoxifen | An analytical reference standard categorized as an SERM; has been detected… | 25 mg | 27190-25 | More Info |
| Tamoxifen | An analytical reference standard categorized as an SERM; has been detected… | 5 mg | 27190-5 | More Info |
| Tamoxifen (citrate) | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 1 g | 11629-1 | More Info |
| Tamoxifen (citrate) | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 10 g | 11629-10 | More Info |
| Tamoxifen (citrate) | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 5 g | 11629-5 | More Info |
| Tamoxifen (citrate) | An estrogen receptor antagonist (IC50 = 45 nM for the rabbit receptor); re… | 500 mg | 11629-500 | More Info |
| Tamoxifen-d5 | An internal standard for the quantification of tamoxifen by GC- or LC-MS | 1 mg | 18262-1 | More Info |
| Tamoxifen-d5 | An internal standard for the quantification of tamoxifen by GC- or LC-MS | 500 µg | 18262-500 | More Info |
| Tamoxifen N-oxide | A metabolite of tamoxifen that is produced by the action of flavin-contain… | 1 mg | 18642-1 | More Info |
| Tamoxifen N-oxide | A metabolite of tamoxifen that is produced by the action of flavin-contain… | 10 mg | 18642-10 | More Info |
| Tamoxifen N-oxide | A metabolite of tamoxifen that is produced by the action of flavin-contain… | 5 mg | 18642-5 | More Info |
| TAMRA-Amyloid-β (1-28) Peptide (human) (trifluoroacetate salt) | A fluorescently labeled amyloid-β peptide; ex / em = 543 / 572 nm | 100 µg | 27110-100 | More Info |
| TAMRA-Amyloid-β (1-40) Peptide (human) (trifluoroacetate salt) | A fluorescently labeled amyloid-β peptide; ex / em = 543 / 572 | 500 µg | 27413-500 | More Info |
| TAMRA-Amyloid-β (1-42) Peptide (trifluoroacetate salt) | A fluorescently labeled amyloid-β peptide; ex / em = 543 / 572 nm, re… | 1 mg | 27409-1 | More Info |
| Tamsulosin-d4 (hydrochloride) | An internal standard for the quantification of tamsulosin by GC- or LC-MS | 2.5 mg | 28486-25 | More Info |
| Tamsulosin (hydrochloride) | A potent α1-AR antagonist (Ki = 0.229 nM in a radioligand binding as… | 10 mg | 24020-10 | More Info |
| Tamsulosin (hydrochloride) | A potent α1-AR antagonist (Ki = 0.229 nM in a radioligand binding as… | 25 mg | 24020-25 | More Info |
| Tamsulosin (hydrochloride) | A potent α1-AR antagonist (Ki = 0.229 nM in a radioligand binding as… | 5 mg | 24020-5 | More Info |
| Tamsulosin (hydrochloride) | A potent α1-AR antagonist (Ki = 0.229 nM in a radioligand binding as… | 50 mg | 24020-50 | More Info |
| TAN 1364B | A PTP inhibitor; inhibits the activity of the PTPs LMW-PTP, CDC25B, and PT… | 2.5 mg | 27964-25 | More Info |
| TAN 1364B | A PTP inhibitor; inhibits the activity of the PTPs LMW-PTP, CDC25B, and PT… | 500 µg | 27964-500 | More Info |
| Tandospirone | A 5-HT1A partial agonist; selectively binds to 5-HT1A receptors (Ki = 0.02… | 10 mg | 40436-10 | More Info |
| Tandospirone | A 5-HT1A partial agonist; selectively binds to 5-HT1A receptors (Ki = 0.02… | 25 mg | 40436-25 | More Info |
| Tandospirone | A 5-HT1A partial agonist; selectively binds to 5-HT1A receptors (Ki = 0.02… | 5 mg | 40436-5 | More Info |
| Tandospirone | A 5-HT1A partial agonist; selectively binds to 5-HT1A receptors (Ki = 0.02… | 50 mg | 40436-50 | More Info |
| Tandutinib | A potent antagonist of the type III receptor tyrosine kinases PDGFRβ,… | 100 mg | 12098-100 | More Info |
| Tandutinib | A potent antagonist of the type III receptor tyrosine kinases PDGFRβ,… | 25 mg | 12098-25 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
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