Welcome to Santa Cruz Biotechnology!

Penicillin G procaine (CAS 6130-64-9)

(Based on popularity)

CAS Number:6130-64-9
Purity:≥98%
Molecular Weight:588.72
Molecular Formula:C29H38N4O6S H2O
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
Penicillin G procaine sc-205797 10 g $34
Penicillin G procaine sc-205797A 25 g $42
Description
Penicillin G procaine is a combination of Penicillin G and Procaine. Penicillin G is a hydrophobic, β-lactam antibiotic produced by Penicillium spp.. As an antibiotic, Penicillin G is noted to posses effectiveness mainly against gram-positive organisms. Some gram-negative organisms such as Neiserria gonorrhoeae and Neiserria meningitidis are also reported to be susceptible to Penicillin G. Penicillin G is also known as benzylpenicillin and contains a 6’ phenylacetyl side chain. In acid aqueous solutions, Penicillin is reported to decompose into penillic acid and penilloic acid.
Procaine is a noted sodium channel blocker with a variety of inhibitory effects. In skeletal muscle, Procaine has been reported to inhibit calcium-induced calcium release (CICR). Procaine is also noted to act as a DNA methylation inhibitor and to cause demethylation and reactivation of methylation-silenced genes such as RARβ and GSTP1. WIF-1 is noted to be reactivated in a cancer cell line and to downregulate the Wnt canonical pathway. In studies utilizing a neuroblastoma cell line (SHEP), Procaine is reported to induce neuronal apoptosis in a manner correlated with lipid solubility of the compound. In an adult mouse muscle cell line (HEK293), the presence of Procaine is reported to potently inhibit nicotinic acetylcholine receptors.

Penicillin G is also available alone (sc-344973) and in salt forms such as Penicillin G sodium (sc-257971) and Penicillin G potassium (sc-255411). Procaine is available alone (sc-296134) and in its salt form, Procaine HCl (sc-250776).
Technical Information
Storage:Store at 4° C
Safety and Reference Information
PubChem CID:22989191
SMILES:CCN(CC)CCOC(=O)C1=CC=C(C=C1)N.CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O) C.O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
References
1. Schwartz, M.A. 1965. J Pharm Sci. 54: 472-473. PMID: 14301592
2. Demain, A.L. 1991. Proc. Natl. Sci. Counc. Repub. China B. 15: 251-265. PMID: 1815263
3. Werdehausen, R., et al. 2009. Br J Anaesth. 103: 711-718. PMID: 19700777
4. Livermore, D.M. 2009. Curr. Protein Pept. Sci. 10: 397-400. PMID: 19538149
5. Gao, Z., et al. 2009. Oncol. Rep. 22: 1479-1484. PMID: 19885602
6. Endo, M. 2009. Physiol. Rev. 89: 1153-1176. PMID: 19789379
7. Wang, H., et al. 2010. Eur. J. Pharmacol. 630: 29-33. PMID: 20045405
8. Gal, R. and Libersat, F. 2010. PLoS ONE. 5: e10019. PMID: 20383324
SDS
Related Product Categories