- Search results for Cay13715-100
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19 products were found matching "Cay13715-100"!
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Item number: Cay13710-1
15(R)-PGE1 is the "unnatural" C-15 stereoisomer of PGE1. It is essentially inactive biologically when compared to PGE1. It is a non-competitive inhibitor of 15-hydroxy PGDH with an IC50 of 189 µM.Formal Name: 9-oxo-11alpha,15R-dihydroxy-prost-13E-en-1-oic acid. CAS Number: 20897-91-0. Synonyms: 15(R)-PGE1, 15-epi...
Keywords: | 15(R)-PGE1, 15-epi PGE1, 9-oxo-11alpha,15R-dihydroxy-prost-13E-en-1-oic acid |
Application: | PGDH inhibitor |
CAS | 20897-91-0 |
MW: | 354.5 D |
From 97.00€
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Item number: Cay173125-100
The CYP1A is a petroleum/PAH/PCB/dioxin-inducible protein (Mr = 55,000-59,000) in liver samples from a wide variety of fish species.Synonyms: C02406101, Cytochrome P450 1A (Cod). Immunogen: Atlantic cod (Gadus morhua L.) CYP1A, purified from liver microsomes of beta-naphthoflavone-treated cod. Formulation: (Request...
Keywords: | C02406101, Cytochrome P450 1A (Cod) |
Application: | ELISA, IHC, WB |
Host: | Mouse |
Species reactivity: | cod |
From 336.00€
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Item number: Cay37151-100
DUN41875 is an inhibitor of stearyol-CoA desaturase 1 (SCD1, IC50 = 11.8 nM for the rat enzyme). It increases tetramerization of soluble alpha-synuclein and reduces mutant alpha-synuclein incorporation into tetramers in BE(2)-M17 neuroblastoma cells expressing a mutant alpha-synuclein containing three...
Keywords: | SCD1 Inhibitor, Stearoyl-CoA Desaturase 1 Inhibitor, Stearoyl-Coenzyme A Desaturase 1 Inhibitor,... |
Application: | Stearoyl-CoA desaturase 1 inhibitor |
CAS | 1295541-87-5 |
MW: | 363.3 D |
From 119.00€
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Item number: Cay13115-500
UR-144 N-(2-chloropentyl) analog is a synthetic cannabinoid which differs from the parent compound, UR-144 (Cay-11502), by the addition of chloride to the 2 position of the pentyl chain. The physiological and toxicological properties of this compound have not been studied. This product is intended for forensic and...
Keywords: | (1-(2-chloropentyl)-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone |
Application: | Analytical reference standard, Synthetic cannabinoid analog |
CAS | 2365471-32-3 |
MW: | 345.9 D |
From 235.00€
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Item number: Cay173135-100
Synonyms: Cytochrome P450 1A (fish). Immunogen: rainbow trout CYP1A amino acid sequence 190-204 and 282-296. Formulation: (Request formulation change), Purified IgG in 0.1 M sodium phosphate, pH 7.4, containing 0.15 M sodium chloride, 12.3 mM sodium azide, and 1% BSA. Host: Rabbit. Applications: ELISA and WB....
Keywords: | Cytochrome P450 1A (fish) |
Application: | ELISA, WB |
Host: | Rabbit |
Species reactivity: | rainbow trout |
From 336.00€
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Item number: Cay10715-100
JWH 018 7-hydroxyindole metabolite-d9 contains nine deuterium atoms at the 2, 2', 3, 3', 4, 4', 5, 5, and 5 positions. It is intended for use as an internal standard for the quantification of JWH 018 7-hydroxyindole metabolite by GC- or LC-mass spectrometry (MS). JWH 018 7-hydroxyindole metabolite is a minor...
Keywords: | (7-hydroxy-1-pentyl-2,2,3,3,4,4,5,5,5-d9-1H-indol-3-yl)-1-naphthalenyl-methanone |
Application: | Analytical reference standard, GC-MS, LC-MS internal standard, Quantification |
CAS | 2749349-17-3 |
MW: | 366.5 D |
From 339.00€
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Item number: Cay23715-100
Didanosine is an antiviral nucleoside analog and an inhibitor of reverse transcriptase. It undergoes cellular amination and phosphorylation to its active triphosphate form, 2',3'-dideoxyadenosine 5'-triphosphate (ddATP, Cay-17460). Didanosine inhibits human T cell leukemia virus type 1 (HTLV-1) reverse transcriptase...
Keywords: | 2',3'-Dideoxyinosine, ddl, NSC 612049, 2',3'-dideoxy-inosine |
Application: | Antiviral nucleoside analog, Reverse transcriptase inhibitor |
CAS | 69655-05-6 |
MW: | 236.2 D |
From 64.00€
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Item number: Cay13175-10
Association of Ras protein with the inner surface of the plasma membrane is required for Ras signaling activity. Farnesyl thiosalicylic acid (FTS) amide is an FTS derivative with an amide added to the carboxyl group. FTS amide inhibits the growth of PANC-1 and U87 tumor cells with IC50 values of 20 and 10 µM,...
Keywords: | FTS Amide, Salirasib Amide, 2-[[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]thio]-benzamide |
Application: | Ras signaling inhibitor |
CAS | 1092521-74-8 |
MW: | 357.6 D |
From 26.00€
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Item number: Cay37150-10
SLF1081851 is an inhibitor of sphingosine-1-phosphate (S1P) transporter (SPNS2). It inhibits mouse Spns2 by 67% when used at a concentration of 2 µM. SLF1081851 inhibits S1P export from HeLa cells expressing mouse Spns2 (IC50 = 1.93 µM). In vivo, SLF1081851 (20 mg/kg) decreases blood lymphocyte numbers and plasma...
Keywords: | 3-(4-decylphenyl)-1,2,4-oxadiazole-5-propanamine, hydrochloride |
Application: | Sphingosine-1-phosphate transporter SPNS2 inhibitor |
MW: | 380 D |
From 101.00€
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Item number: Cay17135-10
Tivantinib is an inhibitor of c-Met (Ki = 0.355 µM). It is selective for c-Met over a panel of 229 additional kinases at 10 µM. Tivantinib also inhibits tubulin polymerization in a cell-free assay in a concentration-dependent manner. It is cytotoxic to c-Met-dependent and -independent cancer cell lines when used at...
Keywords: | ARQ 197, (3R,4R)-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(1H-indol-3-yl)-2,5-pyrrolidinedione |
Application: | Dephosphorylated c-Met kinase binding staurosporine derivative |
CAS | 905854-02-6 |
MW: | 369.4 D |
From 48.00€
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Item number: Cay13713-100
Ion channels are integral membrane proteins that help establish and control the small voltage gradient across the plasma membrane of living cells by allowing the flow of ions down their electrochemical gradient. They are present in the membranes that surround all biological cells and their main function is to...
Keywords: | Anti-KCNQ4, Anti-KQT-like 4, Anti-Potassium channel subunit alpha KvLQT4, Anti-Voltage-gated potassium channel subunit... |
Application: | ICC, IP, WB |
Host: | Mouse |
Species reactivity: | human |
530.00€
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Item number: Cay13100-100
A common metabolic pathway for several prostaglandins (PGs), including prostaglandin D2 (PGD2), involves the reduction of the double bond between C-13 and C-14 and oxidation of the hydroxyl group at C-15, producing 13,14-dihydro-15-keto PGs. The removal of four carbons at the alpha-terminus and oxidation of the...
Keywords: | 9alpha-hydroxy-11,15-dioxo-2,3,4,5-tetranor-prostanoic acid |
Application: | Metabolic studies |
CAS | 1204116-69-7 |
MW: | 298.4 D |
From 141.00€
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