3-O-ethyl-L-Ascorbic Acid |
A tyrosinase inhibitor (IC50s = 16.65 and 29.69 mM for the human and mushr… |
10 g |
34139-10 |
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3-O-ethyl-L-Ascorbic Acid |
A tyrosinase inhibitor (IC50s = 16.65 and 29.69 mM for the human and mushr… |
25 g |
34139-25 |
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3-O-ethyl-L-Ascorbic Acid |
A tyrosinase inhibitor (IC50s = 16.65 and 29.69 mM for the human and mushr… |
5 g |
34139-5 |
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3-O-ethyl-L-Ascorbic Acid |
A tyrosinase inhibitor (IC50s = 16.65 and 29.69 mM for the human and mushr… |
50 g |
34139-50 |
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2-O-ethyl PAF C-16 |
2-O-ethyl PAF C-16 is a synthetic PAF analog which contains an ethyl group… |
1 mg |
60925-1 |
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2-O-ethyl PAF C-16 |
2-O-ethyl PAF C-16 is a synthetic PAF analog which contains an ethyl group… |
10 mg |
60925-10 |
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2-O-ethyl PAF C-16 |
2-O-ethyl PAF C-16 is a synthetic PAF analog which contains an ethyl group… |
25 mg |
60925-25 |
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2-O-ethyl PAF C-16 |
2-O-ethyl PAF C-16 is a synthetic PAF analog which contains an ethyl group… |
5 mg |
60925-5 |
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OF-02 |
An ionizable cationic amino lipid; has been used in combination with other… |
1 mg |
37652-1 |
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OF-02 |
An ionizable cationic amino lipid; has been used in combination with other… |
10 mg |
37652-10 |
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OF-02 |
An ionizable cationic amino lipid; has been used in combination with other… |
5 mg |
37652-5 |
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OF-1 |
A chemical probe for the bromodomains of the BRPF family of proteins; bind… |
1 mg |
17124-1 |
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OF-1 |
A chemical probe for the bromodomains of the BRPF family of proteins; bind… |
10 mg |
17124-10 |
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OF-1 |
A chemical probe for the bromodomains of the BRPF family of proteins; bind… |
25 mg |
17124-25 |
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OF-1 |
A chemical probe for the bromodomains of the BRPF family of proteins; bind… |
5 mg |
17124-5 |
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OF-C4-Deg-Lin |
An ionizable cationic lipid; has been used in the generation of LNPs for t… |
1 mg |
37856-1 |
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OF-C4-Deg-Lin |
An ionizable cationic lipid; has been used in the generation of LNPs for t… |
10 mg |
37856-10 |
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OF-C4-Deg-Lin |
An ionizable cationic lipid; has been used in the generation of LNPs for t… |
5 mg |
37856-5 |
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OF-C4-Deg-Lin |
An ionizable cationic lipid; has been used in the generation of LNPs for t… |
50 mg |
37856-50 |
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OF-Deg-Lin |
An ionizable cationic lipid; has been used in the generation of LNPs for t… |
1 mg |
37853-1 |
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OF-Deg-Lin |
An ionizable cationic lipid; has been used in the generation of LNPs for t… |
10 mg |
37853-10 |
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OF-Deg-Lin |
An ionizable cationic lipid; has been used in the generation of LNPs for t… |
5 mg |
37853-5 |
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Ofloxacin |
A fluoroquinolone antibiotic; prevents supercoiling of bacterial chromosom… |
1 g |
22891-1 |
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Ofloxacin |
A fluoroquinolone antibiotic; prevents supercoiling of bacterial chromosom… |
10 g |
22891-10 |
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Ofloxacin |
A fluoroquinolone antibiotic; prevents supercoiling of bacterial chromosom… |
5 g |
22891-5 |
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Ofloxacin |
A fluoroquinolone antibiotic; prevents supercoiling of bacterial chromosom… |
50 g |
22891-50 |
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Ofloxacin-d8 (hydrochloride) |
An internal standard for the quantification of ofloxacin by GC- or LC-MS |
1 mg |
33466-1 |
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Ofloxacin-d8 (hydrochloride) |
An internal standard for the quantification of ofloxacin by GC- or LC-MS |
5 mg |
33466-5 |
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2''-O-Galloylhyperin |
A natural flavonoid; scavenges DPPH and ABTS radicals (IC50s = 3 and 3.5 &… |
1 mg |
29086-1 |
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2''-O-Galloylhyperin |
A natural flavonoid; scavenges DPPH and ABTS radicals (IC50s = 3 and 3.5 &… |
10 mg |
29086-10 |
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2''-O-Galloylhyperin |
A natural flavonoid; scavenges DPPH and ABTS radicals (IC50s = 3 and 3.5 &… |
25 mg |
29086-25 |
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2''-O-Galloylhyperin |
A natural flavonoid; scavenges DPPH and ABTS radicals (IC50s = 3 and 3.5 &… |
5 mg |
29086-5 |
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Ogerin |
A positive allosteric modulator of GPR68; increases proton-induced cAMP pr… |
1 mg |
34228-1 |
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Ogerin |
A positive allosteric modulator of GPR68; increases proton-induced cAMP pr… |
10 mg |
34228-10 |
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Ogerin |
A positive allosteric modulator of GPR68; increases proton-induced cAMP pr… |
25 mg |
34228-25 |
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Ogerin |
A positive allosteric modulator of GPR68; increases proton-induced cAMP pr… |
5 mg |
34228-5 |
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OGG1-IN-O8 |
An OGG1 inhibitor (IC50 = 0.35 µM); selective for OGG1 over NEIL1, N… |
1 mg |
29769-1 |
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OGG1-IN-O8 |
An OGG1 inhibitor (IC50 = 0.35 µM); selective for OGG1 over NEIL1, N… |
10 mg |
29769-10 |
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OGG1-IN-O8 |
An OGG1 inhibitor (IC50 = 0.35 µM); selective for OGG1 over NEIL1, N… |
25 mg |
29769-25 |
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OGG1-IN-O8 |
An OGG1 inhibitor (IC50 = 0.35 µM); selective for OGG1 over NEIL1, N… |
5 mg |
29769-5 |
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OG-L002 |
A potent inhibitor of LSD1 (IC50 = 0.02 µM) that less effectively in… |
1 mg |
17471-1 |
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OG-L002 |
A potent inhibitor of LSD1 (IC50 = 0.02 µM) that less effectively in… |
10 mg |
17471-10 |
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OG-L002 |
A potent inhibitor of LSD1 (IC50 = 0.02 µM) that less effectively in… |
25 mg |
17471-25 |
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OG-L002 |
A potent inhibitor of LSD1 (IC50 = 0.02 µM) that less effectively in… |
5 mg |
17471-5 |
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OGT 2115 |
An inhibitor of heparanase (IC50 = 0.4 µM); inhibits HSV-2 infection… |
10 mg |
17324-10 |
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OGT 2115 |
An inhibitor of heparanase (IC50 = 0.4 µM); inhibits HSV-2 infection… |
25 mg |
17324-25 |
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OGT 2115 |
An inhibitor of heparanase (IC50 = 0.4 µM); inhibits HSV-2 infection… |
5 mg |
17324-5 |
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OH-C-Chol |
A cationic cholesterol derivative; has been used in lipoplexes with DOPE f… |
1 mg |
26587-1 |
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OH-C-Chol |
A cationic cholesterol derivative; has been used in lipoplexes with DOPE f… |
500 µg |
26587-500 |
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OH-Chol |
A cationic cholesterol derivative; has been used in lipoplexes with DOPE f… |
1 mg |
26586-1 |
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