CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 2 of 644
Non-Antibody Products
Page 2 of 644
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 1 mg | 18396-1 | More Info |
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 10 mg | 18396-10 | More Info |
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 25 mg | 18396-25 | More Info |
| A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 5 mg | 18396-5 | More Info |
| A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 10 mg | 14404-10 | More Info |
| A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 25 mg | 14404-25 | More Info |
| A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 5 mg | 14404-5 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 1 mg | 32855-1 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 10 mg | 32855-10 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 25 mg | 32855-25 | More Info |
| A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 5 mg | 32855-5 | More Info |
| A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 1 mg | 11606-1 | More Info |
| A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 10 mg | 11606-10 | More Info |
| A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 5 mg | 11606-5 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 10 mg | 10012588-10 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 100 mg | 10012588-100 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 5 mg | 10012588-5 | More Info |
| A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 50 mg | 10012588-50 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 10 mg | 20060-10 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 25 mg | 20060-25 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 5 mg | 20060-5 | More Info |
| A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 50 mg | 20060-50 | More Info |
| A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 1 mg | 11163-1 | More Info |
| A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 10 mg | 11163-10 | More Info |
| A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 5 mg | 11163-5 | More Info |
| A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 1 mg | 13898-1 | More Info |
| A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 10 mg | 13898-10 | More Info |
| A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 5 mg | 13898-5 | More Info |
| A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 1 mg | 30934-1 | More Info |
| A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 10 mg | 30934-10 | More Info |
| A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 5 mg | 30934-5 | More Info |
| A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 1 mg | 21807-1 | More Info |
| A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 10 mg | 21807-10 | More Info |
| A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 5 mg | 21807-5 | More Info |
| A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 10 mg | 32974-10 | More Info |
| A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 100 mg | 32974-100 | More Info |
| A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 50 mg | 32974-50 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 1 mg | 10012708-1 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 10 mg | 10012708-10 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 25 mg | 10012708-25 | More Info |
| A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 5 mg | 10012708-5 | More Info |
| A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 10 mg | 19123-10 | More Info |
| A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 5 mg | 19123-5 | More Info |
| A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 50 mg | 19123-50 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 1 mg | 26378-1 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 10 mg | 26378-10 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 25 mg | 26378-25 | More Info |
| A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 5 mg | 26378-5 | More Info |
| A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 10 mg | 15207-10 | More Info |
| A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 25 mg | 15207-25 | More Info |
| A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 5 mg | 15207-5 | More Info |
| A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 50 mg | 15207-50 | More Info |
| A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 1 mg | 25326-1 | More Info |
| A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 10 mg | 25326-10 | More Info |
| A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 25 mg | 25326-25 | More Info |
| A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 5 mg | 25326-5 | More Info |
| A1-28 | An ionizable cationic lipid; has been used in the generation of LNPs for t… | 1 mg | 39590-1 | More Info |
| A1-28 | An ionizable cationic lipid; has been used in the generation of LNPs for t… | 5 mg | 39590-5 | More Info |
| A1-28 | An ionizable cationic lipid; has been used in the generation of LNPs for t… | 500 µg | 39590-500 | More Info |
| A-39183A | An antibiotic; produced by aerobic fermentation of Streptomyces NRRL 12049… | 1 mg | 23239-1 | More Info |
| A-39183A | An antibiotic; produced by aerobic fermentation of Streptomyces NRRL 12049… | 5 mg | 23239-5 | More Info |
| A-54556A | An ADEP antibiotic; active against B. subtilis, S. pyogenes, and E. faecal… | 1 mg | 15305-1 | More Info |
| A-54556A | An ADEP antibiotic; active against B. subtilis, S. pyogenes, and E. faecal… | 5 mg | 15305-5 | More Info |
| AA147 | An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… | 10 mg | 27143-10 | More Info |
| AA147 | An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… | 100 mg | 27143-100 | More Info |
| AA147 | An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… | 5 mg | 27143-5 | More Info |
| AA147 | An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… | 50 mg | 27143-50 | More Info |
| AA26-8 | A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… | 10 mg | 36937-10 | More Info |
| AA26-8 | A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… | 25 mg | 36937-25 | More Info |
| AA26-8 | A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… | 5 mg | 36937-5 | More Info |
| AA26-8 | A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… | 50 mg | 36937-50 | More Info |
| AA-861 | A 5-LO inhibitor (IC50 = 0.8 µM); >100-fold selective for 5-LO over… | 1 mg | 13263-1 | More Info |
| AA-861 | A 5-LO inhibitor (IC50 = 0.8 µM); >100-fold selective for 5-LO over… | 500 µg | 13263-500 | More Info |
| AA92593 | An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… | 10 mg | 35836-10 | More Info |
| AA92593 | An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… | 25 mg | 35836-25 | More Info |
| AA92593 | An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… | 5 mg | 35836-5 | More Info |
| AA92593 | An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… | 50 mg | 35836-50 | More Info |
| AA43279 | An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… | 10 mg | 40428-10 | More Info |
| AA43279 | An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… | 25 mg | 40428-25 | More Info |
| AA43279 | An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… | 5 mg | 40428-5 | More Info |
| AA43279 | An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… | 50 mg | 40428-50 | More Info |
| AAA | A GPR75 antagonist; increases basal GPR75 protein levels and inhibits 20-H… | 1 mg | 32733-1 | More Info |
| AAA | A GPR75 antagonist; increases basal GPR75 protein levels and inhibits 20-H… | 500 µg | 32733-500 | More Info |
| 7-AAD/CFSE Cell-Mediated Cytotoxicity Assay Kit | Cayman's 7-AAD / CFSE Cell-Mediated Cytotoxicity Assay Kit employs CFSE to… | 1 ea | 600120-1EA | More Info |
| AA3-DLin | An ionizable cationic amino lipid (pKa = 5.8); has been used in combinatio… | 10 mg | 37903-10 | More Info |
| AA3-DLin | An ionizable cationic amino lipid (pKa = 5.8); has been used in combinatio… | 25 mg | 37903-25 | More Info |
| AA3-DLin | An ionizable cationic amino lipid (pKa = 5.8); has been used in combinatio… | 5 mg | 37903-5 | More Info |
| AAF-CMK (trifluoroacetate salt) | An irreversible inhibitor of TPPII commonly used at 10-100 µM; does… | 10 mg | 14461-10 | More Info |
| AAF-CMK (trifluoroacetate salt) | An irreversible inhibitor of TPPII commonly used at 10-100 µM; does… | 25 mg | 14461-25 | More Info |
| AAF-CMK (trifluoroacetate salt) | An irreversible inhibitor of TPPII commonly used at 10-100 µM; does… | 5 mg | 14461-5 | More Info |
| 17-AAG | An inhibitor of Hsp90 (IC50s = 5 and 943 nM for BT474 tumor cell and fibro… | 1 mg | 11039-1 | More Info |
| 17-AAG | An inhibitor of Hsp90 (IC50s = 5 and 943 nM for BT474 tumor cell and fibro… | 10 mg | 11039-10 | More Info |
| 17-AAG | An inhibitor of Hsp90 (IC50s = 5 and 943 nM for BT474 tumor cell and fibro… | 5 mg | 11039-5 | More Info |
| AAL-993 | A potent inhibitor of VEGF receptors, inhibiting VEGFR1, 2, and 3 with IC5… | 1 mg | 16351-1 | More Info |
| AAL-993 | A potent inhibitor of VEGF receptors, inhibiting VEGFR1, 2, and 3 with IC5… | 5 mg | 16351-5 | More Info |
| (9,10a)-anti-Δ6a,7-THC | An analytical reference standard that is structurally similar to known phy… | 1 mg | 37046-1 | More Info |
| (9,10a)-anti-Δ6a,7-THC | An analytical reference standard that is structurally similar to known phy… | 5 mg | 37046-5 | More Info |
| AAPH | A water-soluble azo compound used extensively as a free radical generator | 10 g | 82235-10 | More Info |
| AAPH | A water-soluble azo compound used extensively as a free radical generator | 5 g | 82235-5 | More Info |
| A2AR Agonist-1 | An agonist of the adenosine A2A receptor and an inhibitor of ENT1 (Kis = 4… | 1 mg | 28414-1 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
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