6-FAM SE is an amine-reactive succinimidyl ester carboxyfluorescein that yields carboxyamides which are more resistant to hydrolysis than fluorescein conjugates prepared with FITC.

6-FAM SE is an amine-reactive succinimidyl ester carboxyfluorescein that yields carboxyamides which are more resistant to hydrolysis than fluorescein conjugates prepared with FITC.

6-FAM SE is an amine-reactive succinimidyl ester carboxyfluorescein that yields carboxyamides which are more resistant to hydrolysis than fluorescein conjugates prepared with FITC.

6-FITC, a derivative of fluorescein, is generally used in flow cytometry.

6-FITC, a derivative of fluorescein, is generally used in flow cytometry.

6-FITC, a derivative of fluorescein, is generally used in flow cytometry.

6-Hydroxy-2,6-dimethyl-2,7-octadienoic acid is a natural product isolated and purified from the herbs of Hippophae rhamnoides.

6-Hydroxy-2,6-dimethyl-2,7-octadienoic acid is a natural product isolated and purified from the herbs of Hippophae rhamnoides.

6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2].

6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2].

6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2].

6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2].

6-Hydroxyrubiadin is a natural product isolated and purified from the roots of Rubia cordifolia L..

6-Mercaptopurine-9-β-D-ribofuranoside is a purine antimetabolite, acts as an anti-adipogenesis agent, downregulates mRNA levels of PPAR γ and C/EBPα, as well as PPAR γ target protein such as LPL, CD36, aP2, and LXRα[1][2].

6-Mercaptopurine-9-β-D-ribofuranoside is a purine antimetabolite, acts as an anti-adipogenesis agent, downregulates mRNA levels of PPAR γ and C/EBPα, as well as PPAR γ target protein such as LPL, CD36, aP2, and LXRα[1][2].

6-Mercaptopurine-9-β-D-ribofuranoside is a purine antimetabolite, acts as an anti-adipogenesis agent, downregulates mRNA levels of PPAR γ and C/EBPα, as well as PPAR γ target protein such as LPL, CD36, aP2, and LXRα[1][2].

6-Mercaptopurine-9-β-D-ribofuranoside is a purine antimetabolite, acts as an anti-adipogenesis agent, downregulates mRNA levels of PPAR γ and C/EBPα, as well as PPAR γ target protein such as LPL, CD36, aP2, and LXRα[1][2].

6-Methoxy-2-naphthoic acid is an modulator of NMDAR.

6-Methoxynaringenin is a natural product isolated and purified from the herbs of Humulus lupulus.

6-Methoxynaringenin is a natural product isolated and purified from the herbs of Humulus lupulus.

6-Methylflavone is an activator of α1β2γ2L and α1β2 GABAA receptors.

6-OAU is a surrogate agonist of GPR84 activating human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.

6-OAU is a surrogate agonist of GPR84 activating human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.

6-OAU is a surrogate agonist of GPR84 activating human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.

6-OAU is a surrogate agonist of GPR84 activating human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.

6-OAU is a surrogate agonist of GPR84 activating human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.

6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.

6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.

6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.

6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.

6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.

6-ROX is a fluorescent oligonucleotide marker, acts as an acceptor molecule coupled to 5-FAM as the donor in FRET imaging.