CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 734 of 859
Non-Antibody Products
Page 734 of 859
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Sevoflurane | A halogenated ether with anesthetic properties; enhances the activity of G… | 10 g | 23996-10 | More Info |
| Sevoflurane | A halogenated ether with anesthetic properties; enhances the activity of G… | 25 g | 23996-25 | More Info |
| Sevoflurane | A halogenated ether with anesthetic properties; enhances the activity of G… | 5 g | 23996-5 | More Info |
| Sevoflurane | A halogenated ether with anesthetic properties; enhances the activity of G… | 50 g | 23996-50 | More Info |
| SEW2871 | A potent, selective S1P1 receptor agonist; selective for the S1P1 receptor… | 10 mg | 10006440-10 | More Info |
| SEW2871 | A potent, selective S1P1 receptor agonist; selective for the S1P1 receptor… | 25 mg | 10006440-25 | More Info |
| SEW2871 | A potent, selective S1P1 receptor agonist; selective for the S1P1 receptor… | 5 mg | 10006440-5 | More Info |
| SEW2871 | A potent, selective S1P1 receptor agonist; selective for the S1P1 receptor… | 50 mg | 10006440-50 | More Info |
| SF11 | An antagonist of NPY receptor Y2 (IC50 = 0.199 µM); selective for Y2… | 1 mg | 33355-1 | More Info |
| SF11 | An antagonist of NPY receptor Y2 (IC50 = 0.199 µM); selective for Y2… | 10 mg | 33355-10 | More Info |
| SF11 | An antagonist of NPY receptor Y2 (IC50 = 0.199 µM); selective for Y2… | 5 mg | 33355-5 | More Info |
| SF1670 | Inhibits PTEN activity (IC50 = 2 µM), increasing cellular PIP3 level… | 1 mg | 15368-1 | More Info |
| SF1670 | Inhibits PTEN activity (IC50 = 2 µM), increasing cellular PIP3 level… | 5 mg | 15368-5 | More Info |
| SF2523 | A dual inhibitor of PI3K and BRD4 (IC50s = 16, and 241 and 1,550 nM for PI… | 1 mg | 21638-1 | More Info |
| SF2523 | A dual inhibitor of PI3K and BRD4 (IC50s = 16, and 241 and 1,550 nM for PI… | 10 mg | 21638-10 | More Info |
| SF2523 | A dual inhibitor of PI3K and BRD4 (IC50s = 16, and 241 and 1,550 nM for PI… | 5 mg | 21638-5 | More Info |
| SF2523 | A dual inhibitor of PI3K and BRD4 (IC50s = 16, and 241 and 1,550 nM for PI… | 500 µg | 21638-500 | More Info |
| SF7-AM | A cell-trappable fluorogenic probe for the detection of H2S; reaction of t… | 1 mg | 14623-1 | More Info |
| S-Farnesyl Thioacetic Acid | A competitive inhibitor of isoprenylated protein methyltransferase (also k… | 1 mg | 63260-1 | More Info |
| S-Farnesyl Thioacetic Acid | A competitive inhibitor of isoprenylated protein methyltransferase (also k… | 10 mg | 63260-10 | More Info |
| S-Farnesyl Thioacetic Acid | A competitive inhibitor of isoprenylated protein methyltransferase (also k… | 5 mg | 63260-5 | More Info |
| S-Farnesyl Thioacetic Acid | A competitive inhibitor of isoprenylated protein methyltransferase (also k… | 50 mg | 63260-50 | More Info |
| 15(S)-Fluprostenol | (+)-15(R)-Fluprostenol isopropyl ester is a prodrug (Travoprost) which is… | 1 mg | 16787-1 | More Info |
| 15(S)-Fluprostenol | (+)-15(R)-Fluprostenol isopropyl ester is a prodrug (Travoprost) which is… | 10 mg | 16787-10 | More Info |
| 15(S)-Fluprostenol | (+)-15(R)-Fluprostenol isopropyl ester is a prodrug (Travoprost) which is… | 5 mg | 16787-5 | More Info |
| 15(S)-Fluprostenol isopropyl ester | Unnatural C-15 epimer of Travoprost | 1 mg | 16788-1 | More Info |
| 15(S)-Fluprostenol isopropyl ester | Unnatural C-15 epimer of Travoprost | 10 mg | 16788-10 | More Info |
| 15(S)-Fluprostenol isopropyl ester | Unnatural C-15 epimer of Travoprost | 5 mg | 16788-5 | More Info |
| (S)-Flurbiprofen | The active enantiomer of flurbiprofen (IC50s = 0.48 and 0.47 µM for… | 1 g | 10004207-1 | More Info |
| (S)-Flurbiprofen | The active enantiomer of flurbiprofen (IC50s = 0.48 and 0.47 µM for… | 100 mg | 10004207-100 | More Info |
| (S)-Flurbiprofen | The active enantiomer of flurbiprofen (IC50s = 0.48 and 0.47 µM for… | 250 mg | 10004207-250 | More Info |
| (S)-Flurbiprofen | The active enantiomer of flurbiprofen (IC50s = 0.48 and 0.47 µM for… | 500 mg | 10004207-500 | More Info |
| sFRP1 (human, recombinant) | Source: Active recombinant human C-terminal His-tagged sFRP1 expressed in… | 50 µg | 38061-50 | More Info |
| SGA360 | A selective modulator of AhR; competitively binds AhR (IC50 = 3 µM);… | 1 mg | 21986-1 | More Info |
| SGA360 | A selective modulator of AhR; competitively binds AhR (IC50 = 3 µM);… | 10 mg | 21986-10 | More Info |
| SGA360 | A selective modulator of AhR; competitively binds AhR (IC50 = 3 µM);… | 25 mg | 21986-25 | More Info |
| SGA360 | A selective modulator of AhR; competitively binds AhR (IC50 = 3 µM);… | 5 mg | 21986-5 | More Info |
| SGC0946 | A potent inhibitor of DOT1L (IC50 = 0.3 nM); over 100-fold selective over… | 10 mg | 13967-10 | More Info |
| SGC0946 | A potent inhibitor of DOT1L (IC50 = 0.3 nM); over 100-fold selective over… | 25 mg | 13967-25 | More Info |
| SGC0946 | A potent inhibitor of DOT1L (IC50 = 0.3 nM); over 100-fold selective over… | 5 mg | 13967-5 | More Info |
| SGC0946 | A potent inhibitor of DOT1L (IC50 = 0.3 nM); over 100-fold selective over… | 50 mg | 13967-50 | More Info |
| SGC3027 | A prodrug form of the PRMT7 inhibitor SGC8158; converted by intracellular… | 1 mg | 25325-1 | More Info |
| SGC3027 | A prodrug form of the PRMT7 inhibitor SGC8158; converted by intracellular… | 10 mg | 25325-10 | More Info |
| SGC3027 | A prodrug form of the PRMT7 inhibitor SGC8158; converted by intracellular… | 5 mg | 25325-5 | More Info |
| SGC707 | A potent allosteric inhibitor of PRMT3 (IC50 = 50 nM) with >100-fold selec… | 1 mg | 17017-1 | More Info |
| SGC707 | A potent allosteric inhibitor of PRMT3 (IC50 = 50 nM) with >100-fold selec… | 10 mg | 17017-10 | More Info |
| SGC707 | A potent allosteric inhibitor of PRMT3 (IC50 = 50 nM) with >100-fold selec… | 25 mg | 17017-25 | More Info |
| SGC707 | A potent allosteric inhibitor of PRMT3 (IC50 = 50 nM) with >100-fold selec… | 50 mg | 17017-50 | More Info |
| SGC-CBP30 | A potent inhibitor of CREBBP and EP300 bromodomains (IC50s = 21-69 and 38… | 10 mg | 14469-10 | More Info |
| SGC-CBP30 | A potent inhibitor of CREBBP and EP300 bromodomains (IC50s = 21-69 and 38… | 5 mg | 14469-5 | More Info |
| SGC-CBP30 | A potent inhibitor of CREBBP and EP300 bromodomains (IC50s = 21-69 and 38… | 50 mg | 14469-50 | More Info |
| SGC-CK2-1 | A CK2α inhibitor (IC50s = 4.2 and 2.3 for the catalytic subunits CK2… | 1 mg | 34103-1 | More Info |
| SGC-CK2-1 | A CK2α inhibitor (IC50s = 4.2 and 2.3 for the catalytic subunits CK2… | 10 mg | 34103-10 | More Info |
| SGC-CK2-1 | A CK2α inhibitor (IC50s = 4.2 and 2.3 for the catalytic subunits CK2… | 25 mg | 34103-25 | More Info |
| SGC-CK2-1 | A CK2α inhibitor (IC50s = 4.2 and 2.3 for the catalytic subunits CK2… | 5 mg | 34103-5 | More Info |
| SGC-GAK-1 | A GAK inhibitor (Ki = 3.1 nM); >50-fold selective for GAK over a panel of… | 10 mg | 33229-10 | More Info |
| SGC-GAK-1 | A GAK inhibitor (Ki = 3.1 nM); >50-fold selective for GAK over a panel of… | 25 mg | 33229-25 | More Info |
| SGC-GAK-1 | A GAK inhibitor (Ki = 3.1 nM); >50-fold selective for GAK over a panel of… | 5 mg | 33229-5 | More Info |
| SGC-GAK-1 | A GAK inhibitor (Ki = 3.1 nM); >50-fold selective for GAK over a panel of… | 50 mg | 33229-50 | More Info |
| SGC2085 (hydrochloride) | A PRMT4 / CARM1 inhibitor (IC50 = 50 nM); highly selective for PRMT4 / CAR… | 1 mg | 21879-1 | More Info |
| SGC2085 (hydrochloride) | A PRMT4 / CARM1 inhibitor (IC50 = 50 nM); highly selective for PRMT4 / CAR… | 10 mg | 21879-10 | More Info |
| SGC2085 (hydrochloride) | A PRMT4 / CARM1 inhibitor (IC50 = 50 nM); highly selective for PRMT4 / CAR… | 5 mg | 21879-5 | More Info |
| SGC2085 (hydrochloride) | A PRMT4 / CARM1 inhibitor (IC50 = 50 nM); highly selective for PRMT4 / CAR… | 500 µg | 21879-500 | More Info |
| SGC-iMLLT | An inhibitor of the YEATS domain-containing proteins MLLT1 and MLLT3; bind… | 1 mg | 28113-1 | More Info |
| SGC-iMLLT | An inhibitor of the YEATS domain-containing proteins MLLT1 and MLLT3; bind… | 10 mg | 28113-10 | More Info |
| SGC-iMLLT | An inhibitor of the YEATS domain-containing proteins MLLT1 and MLLT3; bind… | 5 mg | 28113-5 | More Info |
| SGC Probe Set | Contains a collection of small, drug-like molecules that inhibit or antago… | 1 ea | 17748-1EA | More Info |
| SGC-SMARCA-BRDVIII | A pan-family VIII BRD inhibitor; selectively binds to PBRM1 bromodomain 5,… | 1 mg | 33567-1 | More Info |
| SGC-SMARCA-BRDVIII | A pan-family VIII BRD inhibitor; selectively binds to PBRM1 bromodomain 5,… | 10 mg | 33567-10 | More Info |
| SGC-SMARCA-BRDVIII | A pan-family VIII BRD inhibitor; selectively binds to PBRM1 bromodomain 5,… | 25 mg | 33567-25 | More Info |
| SGC-SMARCA-BRDVIII | A pan-family VIII BRD inhibitor; selectively binds to PBRM1 bromodomain 5,… | 5 mg | 33567-5 | More Info |
| S-Geranylgeranyl-L-glutathione | A P2RY8 ligand; selectively induces internalization of P2RY8 over S1P2, GP… | 1 mg | 9004116-1 | More Info |
| S-Geranylgeranyl-L-glutathione | A P2RY8 ligand; selectively induces internalization of P2RY8 over S1P2, GP… | 10 mg | 9004116-10 | More Info |
| S-Geranylgeranyl-L-glutathione | A P2RY8 ligand; selectively induces internalization of P2RY8 over S1P2, GP… | 5 mg | 9004116-5 | More Info |
| SGI-1027 | An inhibitor of the DNA methyltransferases DNMT1, DNMT3A, and DNMT3B (IC50… | 1 mg | 11165-1 | 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
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