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12706-94-4

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  • 2(1H)-Pyrimidinone,4-amino-1-[4-amino-6-O-(3-amino-3-deoxy-b-D-glucopyranosyl)-4-deoxy-D-glycero-D-galacto-b-D-gluco-undecopyranosyl]-

    Cas No: 12706-94-4

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  • 4-amino-1-[5-amino-6-[1-[4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6-pentahydroxyhexyl]-3,4-dihydroxyoxan-2-yl]pyrimidin-2-one

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  • 2(1H)-Pyrimidinone,4-amino-1-[4-amino-6-O-(3-amino-3-deoxy-b-D-glucopyranosyl)-4-deoxy-D-glycero-D-galacto-b-D-gluco-undecopyranosyl]- cas 12706-94-4

    Cas No: 12706-94-4

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12706-94-4 Usage

Definition

ChEBI: A nucleoside antibiotic with anthelminthic properties that is isolated from Streptomyces longissimus.

Safety Profile

Poison by ingestion andintravenous routes. When heated to decomposition itemits toxic fumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 12706-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,7,0 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 12706-94:
(7*1)+(6*2)+(5*7)+(4*0)+(3*6)+(2*9)+(1*4)=94
94 % 10 = 4
So 12706-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H37N5O14/c22-7-1-2-26(21(37)25-7)19-16(36)12(32)9(24)17(39-19)18(15(35)14(34)10(30)5(29)3-27)40-20-13(33)8(23)11(31)6(4-28)38-20/h1-2,5-6,8-20,27-36H,3-4,23-24H2,(H2,22,25,37)/t5-,6+,8-,9-,10-,11+,12-,13+,14-,15-,16+,17-,18?,19+,20-/m0/s1

12706-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name hikizimycin

1.2 Other means of identification

Product number -
Other names anthelmycine

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:12706-94-4 SDS

12706-94-4Downstream Products

12706-94-4Related news

The structure of hikizimycin (cas 12706-94-4) : Part I. Identification of 3-amino-3-deoxy-D-glucose and cytosine as structural components☆08/25/2019

The molecular formula for hikizimycin, a new antibiotic isolated from Streptomyces A-5, is now established as C21H37N5O14. Evidence in support of the occurrence of 3-amino-3-deoxy-D-glucose and cytosine residues in the antibiotic molecules is presented. Methanolysis of N,N′-diacetylhikizimycin ...detailed

13C NMR investigations of the nucleoside antibiotic hikizimycin (cas 12706-94-4) and its constituents08/23/2019

Confirmation of the structure of the nucleoside antibiotic hikizimycin was obtained by comparing the 13C NMR chemical shift data of selected model compounds with hikizimycin and its constituents.detailed

12706-94-4Relevant articles and documents

Convergent Total Synthesis of Hikizimycin Enabled by Intermolecular Radical Addition to Aldehyde

Fujino, Haruka,Fukuda, Takumi,Nagatomo, Masanori,Inoue, Masayuki

supporting information, p. 13227 - 13234 (2020/09/01)

Hikizimycin (1), which exhibits powerful anthelmintic activity, has the most densely functionalized structure among nucleoside antibiotics. A central 4-amino-4-deoxyundecose of 1 possesses 10 contiguous stereocenters on a C1-C11 linear chain and is decora

Total synthesis of the anthelmintic agent hikizimycin

Ikemoto, Norihiro,Schreiber, Stuart L.

, p. 9657 - 9659 (2007/10/02)

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