GHSR

阻害剤の選択性比較

カタログ番号 製品カタログ 溶解度(25°C)
DMSO アルコール
S6948 Lanreotide 100 mg/mL 100 mg/mL 100 mg/mL
S4980 Anamorelin <1 mg/mL 100 mg/mL 79 mg/mL
S1151 Ibutamoren mesylate 100 mg/mL 100 mg/mL 100 mg/mL
S0169 Capromorelin tartrate 100 mg/mL 100 mg/mL '''100 mg/mL

GHSR製品

製品コード 製品説明 文献中Selleckの製品使用例 お客様のフィードバック
S6948

Lanreotide

Lanreotide (Laromustine, Angiopeptin, BIM 23014, Dermopeptin, Ipstyl, ITM-014, Somatulina, Somatuline, Lanreotidum), an analog of the native somatostatin peptide, is a physiological inhibitor of growth hormone (GH). Lanreotide also has antitumoral effects.

S4980

Anamorelin

Anamorelin (ONO-7643, RC-1291, ST-1291) is an orally active, high-affinity, selective agonist of the ghrelin receptor with an EC50 value of 0.74 nM in the HEK293/GRLN FLIPR assay.

S1151

Ibutamoren mesylate

A potent, orally active growth hormone (GH) secretagogue.

S0169

Capromorelin tartrate

Capromorelin Tartrate (CP 424391-18), a member of the growth hormone secretagogue (GHS) class of drugs, is a ghrelin receptor agonist and a novel therapy for stimulation of appetite in dogs with Ki of 7 nM for hGHS-R1a and EC50 of 3 nM for rat pituicyte.

製品コード 製品説明 文献中Selleckの製品使用例 お客様のフィードバック
S6948

Lanreotide

Lanreotide (Laromustine, Angiopeptin, BIM 23014, Dermopeptin, Ipstyl, ITM-014, Somatulina, Somatuline, Lanreotidum), an analog of the native somatostatin peptide, is a physiological inhibitor of growth hormone (GH). Lanreotide also has antitumoral effects.

製品コード 製品説明 文献中Selleckの製品使用例 お客様のフィードバック
S4980

Anamorelin

Anamorelin (ONO-7643, RC-1291, ST-1291) is an orally active, high-affinity, selective agonist of the ghrelin receptor with an EC50 value of 0.74 nM in the HEK293/GRLN FLIPR assay.

2020, 10.1002/dta.2917

S1151

Ibutamoren mesylate

A potent, orally active growth hormone (GH) secretagogue.

S0169

Capromorelin tartrate

Capromorelin Tartrate (CP 424391-18), a member of the growth hormone secretagogue (GHS) class of drugs, is a ghrelin receptor agonist and a novel therapy for stimulation of appetite in dogs with Ki of 7 nM for hGHS-R1a and EC50 of 3 nM for rat pituicyte.

2020, 10.1002/dta.2917