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18607-76-6

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18607-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18607-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,0 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18607-76:
(7*1)+(6*8)+(5*6)+(4*0)+(3*7)+(2*7)+(1*6)=126
126 % 10 = 6
So 18607-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H34O6/c1-12(22)19(25)8-9-21(27)18(19,3)16(24)11-15-17(2)6-5-14(23)10-13(17)4-7-20(15,21)26/h4,12,14-16,22-27H,5-11H2,1-3H3/t12?,14-,15+,16+,17-,18+,19-,20?,21+/m0/s1

18607-76-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ornogenin

1.2 Other means of identification

Product number -
Other names sarcostin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18607-76-6 SDS

18607-76-6Upstream product

18607-76-6Relevant articles and documents

Pregnane glycosides from Gymnema inodorum and their α-glucosidase inhibitory activity

Trang, Do Thi,Yen, Duong Thi Hai,Cuong, Nguyen The,Anh, Luu The,Hoai, Nguyen Thi,Tai, Bui Huu,Doan, Vu Van,Yen, Pham Hai,Quang, Tran Hong,Nhiem, Nguyen Xuan,Minh, Chau Van,Kiem, Phan Van

, p. 2157 - 2163 (2019/11/03)

Two new pregnane glycosides, gyminosides A and B (1 and 2) and three known, tinctoroside B (3), tinctoroside C (4), and gymnepregoside F (5) were isolated from the leaves of Gymnema inodorum (Lour.) Decne. Their structures were elucidated by physical and chemical methods and comparing with those reported in the literature. All these compounds were evaluated for α-glucosidase assay. Compound 5 exhibited the most anti α-glucosidase activity with inhibitory percentage of 63.7 ± 3.9% at the concentration of 200 μM. Compounds 1–4 showed moderate anti α-glucosidase activity with inhibitory percentage ranging from 40.0 to 52.1%.

The anti-glycative potentials of pregnane glycosides from Gymnema sylvestre

Hung, Nguyen Van,Kiem, Phan Van,Kim, Seung Hyun,Kim, Sun Yeou,Lee, Jae Hyuk,Manh, Hoang Duc,Minh, Chau Van,Nhiem, Nguyen Xuan,Park, SeonJu,Tai, Bui Huu,Trang, Do Thi,Yen, Duong Thi Hai,Yen, Pham Hai

, p. 19 - 24 (2020/05/18)

Gymnema sylvestre is known for its potent antidiabetic activity. Phytochemical investigations of this plant led to the isolation of three new pregnane glycosides, gymnepregosides R-T (1-3) and four known analogues, 12β-acetyloxy-3β,8β,14β,17β-tetrahydroxypregn-5-en-20-one 3-O-β-D-glucopyranosyl-(1→4)-6-deoxy-3-O-methyl-β-D-allopyranosyl-(1→4)-β-D-oleandropyranosyl-(1→4)-β-D-cymaropyranosyl-(1→4)-β-D-cymaropyranoside (4), 12-O-(E)-cinnamoylgymnepregoside F (5), gymnepregoside F (6), and stephanoside I (7). Their structures were identified based on spectroscopic evidence and compared with those reported in the literature. All compounds were evaluated for antiglycative inhibitory activity. Compounds 1, 3, 5, and 6 showed the inhibitory effect on BSA-MGO formation ranging from 6.0 to 8.8 % at the concentrations of 400 μM. Compounds 1 and 2 showed significant breaking properties on MGO-AGE-protein crosslink with percent modification ranging from 54.6 to 58.4 %. Notably, a novel AGEs inhibitor (1) may inhibit the formation and accumulation of MGO-AGEs and protect cells from MGO-AGEs cross-linking damage.

A PREGNANE ESTER AND ITS GLYCOSIDE FROM ORTHENTHERA VIMINEA

Kaur, Kanwal J.,Khare, Maheshwari P.,Khare, Anakshi

, p. 3007 - 3010 (2007/10/02)

A new pregnane ester named ornogenin and its diglycoside designated as ornine were isolated from the dried twigs of Orthenthera viminea.On the basis of chemical and spectroscopic evidence, their structures were established as 12,20-di-O-cinnamoyl-sarcosti

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