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SCH 60057 Sale

目录号 : GC48071

A NK receptor antagonist

SCH 60057 Chemical Structure

Cas No.:203061-35-2

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1 mg
¥2,483.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

SCH 60057 is a fungal metabolite that has been found in Acremonium and a neurokinin receptor (NK) antagonist (IC50s = 6 and 12 µM for NK1 and NK2, respectively).1

1.Hegde, V.R., Dai, P., Chu, M., et al.Neurokinin receptor inhibitors: fermentation, isolation, physico-chemical properties, structure and biological activityJ. Antibiot. (Tokyo)50(12)983-991(1997)

Chemical Properties

Cas No. 203061-35-2 SDF
Canonical SMILES OC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCCC(O)(C)CCCC(O)(C)CCCC(O)(C)CCCC(O)(C)CCCC(O)(C)CC/C=C(C)/C
分子式 C45H84O6 分子量 721.1
溶解度 Dichloromethane: soluble,DMSO: soluble,Ethanol: soluble,Methanol: soluble 储存条件 Store at -20°C
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1 mM 1.3868 mL 6.9339 mL 13.8677 mL
5 mM 0.2774 mL 1.3868 mL 2.7735 mL
10 mM 0.1387 mL 0.6934 mL 1.3868 mL
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Research Update

Neurokinin receptor inhibitors: fermentation, isolation, physico-chemical properties, structure and biological activity

J Antibiot (Tokyo) 1997 Dec;50(12):983-91.PMID:9510903DOI:10.7164/antibiotics.50.983

Seven neurokinin (NK) receptor inhibitors SCH 60059 (1), SCH 60065 (2), SCH 64879 (3), SCH 60061 (4), SCH 60063 (5), SCH 60057 (7), and SCH 64878 (9) and two uncharacterized components 6 and 8, were isolated from the fermentation broth of a fungus taxonomically classified as an Acremonium sp. These compounds were isolated from the fermentation broth by ethyl acetate extraction. Purification and separation of the individual compounds were achieved by NK1 and NK2 assay-guided fractionation using gel filtration, reverse phase chromatography and HPLC. The NK active compounds were identified to be a family of polyhydroxy isoprenoid derivatives, including glycosylated members, by spectroscopic and degradation studies. Compounds 1 approximately 5 and 7 contain nine isoprene units connected in head to tail fashion and compound 9 contains fifteen isoprene units connected in a similar manner. All these compounds showed dual inhibition in NK1 and NK2 assays with IC50 values ranging from 2.5 approximately 11 microM in the NK1 assay and 6.8 approximately 16 microM in the NK2 assay.