Guanine (hydrochloride)


CAS No. : 635-39-2

635-39-2
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Cat. No. : HY-Y1055A
M.Wt: 187.59
Formula: C5H6ClN5O
Purity: >98 %
Solubility: DMSO : 50 mg/mL (ultrasonic;warming;heat to 60°C)
Introduction of 635-39-2 :

Guanine hydrochloride is one of the fundamental components of nucleic acids (DNA and RNA). Guanine hydrochloride is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine hydrochloride has the potential to serve as a large-capacity N pool. Guanine hydrochloride has cytotoxic, antinociceptive and neuroprotective effects[1][2][3][4]. In Vitro:Guanine (1 h) hydrochloride inhibits Shigella dysenteriae type 1 Shiga toxin A subunit in African green monkey Vero cells, with IC50 of 11.5 μM[2].

Guanine (24 h) hydrochloride shows cytotoxicity against African green monkey Vero cells, with CC50 of 136.5 μM[2].
Guanine (10 μM, 16-40 h) hydrochloride partially antagonizes the cytostatic effect of Mycophenolic acid (HY-B0421) on LAN5 cells[3].
In Vivo:Guanine (600 nmol; i.t.) hydrochloride inhibits spinal glutamate- and AMPA-induced biting behaviour in mice[4].
Guanine (200-600 nmol; i.t.) hydrochloride produces A1 adenosine receptor-mediated antinociception against intraplantar glutamate-, Capsaicin (HY-10448)-, and Acetic acid (HY-Y0319)-induced pain in mice, with ID50 values of 107, 84, and 48 nmol and maximal inhibitions of 48%, 58%, and 56%, respectively[4].
Guanine (200-600 nmol; i.t.) hydrochloride produces dose-dependent antinociception against tail-flick test thermal nociception in mice, with peak efficacy at 400 nmol yielding ~78% MPE[4].
Guanine (200-600 nmol; i.t.) hydrochloride dose-dependently increases CSF levels of inosine, xanthine, and uric acid, with a significant increase in AMP at the highest dose[4].

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