추천 제품
Quality Level
분석
97%
광학 활성
[α]22/D +170.0°, c = 1 in chloroform
mp
292-295 °C (lit.)
SMILES string
CC1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@]3(C)[C@@H]2C(=O)C=C4[C@@H]5C[C@](C)(CC[C@]5(C)CC[C@@]34C)C(O)=O
InChI
1S/C30H46O4/c1-25(2)21-8-11-30(7)23(28(21,5)10-9-22(25)32)20(31)16-18-19-17-27(4,24(33)34)13-12-26(19,3)14-15-29(18,30)6/h16,19,21-23,32H,8-15,17H2,1-7H3,(H,33,34)/t19-,21-,22-,23+,26+,27-,28-,29+,30+/m0/s1
InChI key
MPDGHEJMBKOTSU-YKLVYJNSSA-N
유전자 정보
human ... HSD11B1(3290) , HSD11B2(3291)
rat ... Hsd11b1(25116) , Hsd11b2(25117)
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일반 설명
18β-Glycyrrhetinic acid is a pentacyclic triterpenoid found in the Glycyrrhiza glabra L.(liquorice) roots. It is the key metabolite of glycyrrhizin and glycyrrhizic acid.
애플리케이션
The product may be used as a starting material to prepare 18β-glycyrrhetinic acid derivatives, which show anti-inflammatory and antioxidant properties.
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Synthesis, anti-inflammatory, and antioxidant activities of 18?-glycyrrhetinic acid derivatives as chemical mediators and xanthine oxidase inhibitors.
Bioorganic & Medicinal Chemistry, 17(7), 2785-2792 (2009)
Journal of medicinal chemistry, 50(24), 6189-6200 (2007-11-06)
Selective hsp90 inhibitors simultaneously destabilize and deplete key signaling proteins involved in cell proliferation and survival, angiogenesis, and metastasis. Investigation of novobiocin analogues lacking the noviose moiety as novel inhibitors of hsp90 was carried out. A novel series of 3-aminocoumarin
18?-Glycyrrhetinic acid interaction with bovine serum albumin.
Journal of Photochemistry and Photobiology A: Chemistry, 185(2), 271-276 (2007)
From Test Tube to Clinical Trial; Promising Herbs with NF-?B and COX-2 Activity.
Current Immunology Reviews, 10(2), 82-98 (2014)
A robust screening method for dietary agents that activate tumour-suppressor microRNAs.
Scientific Reports, 5 (2015)
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