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28161-50-4

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28161-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28161-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28161-50:
(7*2)+(6*8)+(5*1)+(4*6)+(3*1)+(2*5)+(1*0)=104
104 % 10 = 4
So 28161-50-4 is a valid CAS Registry Number.

28161-50-4Relevant articles and documents

FLAVONONES FROM CYCLOTRICHIUM NIVEUM

Doganca, S.,Ulubelen, A.,Tuzlaci, E.

, p. 3561 - 3562 (1989)

A new flavonone isosakuranetin 7-O-rhamnoside was isolated from Cyclotrichium niveum together with known flavonones isosakuranetin and eriodictyol 7-O-glucoside, the flavonones apigenin, apigenin 7-methyl ether, acacetin 7-O-rutinoside and the triterpenoids vergatic acid, oleanolic acid, β-amyrin and sitosterol.Key Word Index - Cyclotrichium niveum; Labiatea; whole plant; isosakuranetin; isosakuranetin 7-O-rhamnoside; eriodictyol 7-O-glucoside; flavones; triterpenes.

Oleanane-type saponins and prosapogenins from Albizia julibrissin and their cytotoxic activities

Han, Qinghua,Qian, Yi,Wang, Xuda,Zhang, Qingying,Cui, Jingrong,Tu, Pengfei,Liang, Hong

, (2021/04/02)

Two undescribed oleanane-type saponins, julibrosides K–L, along with three undescribed oleanane-type prosapogenins, julibrosides M–O, were isolated from the stem bark of Albizia julibrissin Durazz. and the mild alkaline hydrolysate of the total saponin, r

Melanogenesis-Inhibitory and Cytotoxic Activities of Triterpene Glycoside Constituents from the Bark of Albizia procera

Zhang, Jie,Akihisa, Toshihiro,Kurita, Masahiro,Kikuchi, Takashi,Zhu, Wan-Fang,Ye, Feng,Dong, Zhen-Huan,Liu, Wen-Yuan,Feng, Feng,Xu, Jian

supporting information, p. 2612 - 2620 (2019/01/04)

Five oleanane-type triterpene glycosides including three new ones, proceraosides E-G (1-3), were isolated from a MeOH-soluble extract of Albizia procera bark. The structures of 1-3 were determined by use of NMR spectra, HRESIMS, and chemical methods. Compounds 1-5 exhibited inhibitory activities against the proliferation of the A549, SKBR3, AZ521, and HL60 human cancer cell lines (IC50 0.28-1.8 μM). Additionally, the apoptosis-inducing activity of compound 2 was evaluated by Hoechst 33342 staining and flow cytometry, while the effects of 2 on the activation of caspases-9, -8, and -3 in HL60 cells were revealed by Western blot analysis.

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