Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

51050

Sigma-Aldrich

Guanosine

≥98.0% (HPLC)

Sinonimo/i:

9-(β-D-Ribofuranosyl)guanine, Guanine-9-β-D-ribofuranoside

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula empirica (notazione di Hill):
C10H13N5O5
Numero CAS:
118-00-3
Peso molecolare:
283.24
Beilstein:
625911
Numero CE:
204-227-8
Numero MDL:
MFCD00010182
Codice UNSPSC:
41106305

Saggio

≥98.0% (HPLC)

Attività ottica

[α]20/D −73±2°, c = 1.5% in 0.1 M NaOH

Impurezze

≤3% water

Punto di fusione

250 °C (dec.) (lit.)

Solubilità

0.1 M NaOH: 0.1 g/mL, clear, slightly yellow

Stringa SMILE

[H]O[H].NC1=Nc2c(ncn2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)C(=O)N1

InChI

1S/C10H13N5O5/c11-10-13-7-4(8(19)14-10)12-2-15(7)9-6(18)5(17)3(1-16)20-9/h2-3,5-6,9,16-18H,1H2,(H3,11,13,14,19)/t3-,5-,6-,9-/m1/s1
NYHBQMYGNKIUIF-UUOKFMHZSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
1379265
1373414
1349587
1343816
1296319

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

Jing Xu et al.
Journal of natural products, 74(10), 2224-2230 (2011-09-21)
Ten myrsinol diterpenes, euphorbiaproliferins A-J (1-10), along with nine known analogues (11-19) were isolated from the roots of Euphorbia prolifera. Their structures were elucidated by spectroscopic data analysis (IR, ESIMS, HRESIMS, 1D and 2D NMR), and the structure of 1
Ping Guo et al.
Journal of natural products, 74(7), 1575-1583 (2011-06-21)
Ten new neo-clerodane diterpenes, ajugaciliatins A-J (1-5, 8-12), along with 17 known analogues (6, 7, 13-27) were isolated from the whole plants of Ajuga ciliata Bunge. Their structures were elucidated by spectroscopic data analysis (IR, ESIMS, HRESIMS, 1D and 2D
Yanjie Sun et al.
Antimicrobial agents and chemotherapy, 51(1), 84-88 (2006-10-25)
Ribavirin (RBV) is a broad-spectrum antiviral agent that inhibits the production of infectious Hantaan virus (HTNV). Although the mechanism of action of RBV against HTNV is not understood, RBV is metabolized in human cells to both RBV-5'-monophosphate, which inhibits IMP
Zadkiel Alvarez et al.
Antimicrobial agents and chemotherapy, 54(12), 5329-5336 (2010-10-06)
Bacillus anthracis, the etiological agent of anthrax, has a dormant stage in its life cycle known as the endospore. When conditions become favorable, spores germinate and transform into vegetative bacteria. In inhalational anthrax, the most fatal manifestation of the disease
Craig H Steeves et al.
Bioorganic & medicinal chemistry letters, 21(18), 5188-5190 (2011-08-16)
CTP Synthase from Trypanosoma brucei (TbCTPS) catalyzes the conversion of UTP to CTP and is a recognized target for the development of antiprotozoal agents. GTP activates glutamine-dependent CTP formation catalyzed by TbCTPS at concentrations below 0.2 mM, but inhibits this

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.