PENICILLIN G PROCAINE
Penicillin G procaine is a repository form combining benzylpenicillin with procaine to prolong absorption and provide local anesthetic effect. It is used for moderately severe infections caused by penicillin-sensitive organisms. Side effects include procaine-related CNS symptoms (anxiety, dizziness), injection-site pain, allergic reactions, and, rarely, Hoign syndrome with accidental intravascular injection. Only GMP materials will be supplied, logistics all according to GDP.
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Product Description
Mechanism of Action
PENICILLIN G PROCAINE demonstrates a multidimensional biochemical activity pattern, affecting enzymeregulated catalytic networks, receptormediated intracellular signalling, mitochondrial respiratory pathways, oxidativestress regulation, ionchannel behaviour, cytoskeletal mechanics and transcriptionfactor network modulation. Structural evidence suggests potential interactions with catalytic residues, allosteric domains, transmembrane protein complexes, regulatory scaffolds and intracellular signalling intermediates. These interactions allow PENICILLIN G PROCAINE to influence phosphorylation kinetics, secondmessenger signalling (Ca²⁺, cAMP, IP, DAG), redoxbuffering systems, ATP turnover rates and mitochondrial membranepotential stability.
Depending on experimental conditions, PENICILLIN G PROCAINE may alter metabolic flux distribution, cytoskeletal tension, vesicular transport efficiency, chromatinaccessibility patterns and geneexpression networks related to stress responses, inflammation, apoptosis, autophagy and metabolic adaptation.
Benefits and Advantages
This compound is widely used across highresolution biochemical and pharmacological research areas, including:
- Receptorligand interaction analysis and affinitymapping
- Detailed enzymekinetics profiling and catalyticpathway evaluation
- Mitochondrialdynamics studies, ATPflux modelling and oxidativestress research
- Integrated multiomics applications (transcriptomics, metabolomics, proteomics, phosphoproteomics)
- Cytoskeletal and membranemechanics modelling
- Apoptosis, necroptosis, ferroptosis and autophagy signalling pathway studies
- SAR (structureactivity relationship) and molecularoptimisation pipelines
- Mechanistic pharmacodynamic modelling and thresholdactivation experiments
Side Effects and Risks
Laboratoryobserved risks include:
- Oxidativestress imbalance and ROS overproduction
- Mitochondrial overload or suppression of respiratorychain complexes
- Dysregulation of Na⁺/K⁺/Ca²⁺ transport and ionchannel behaviour
- Unintended receptor crosstalk or inhibitory interference
- Cytoskeletal destabilisation and membrane-integrity compromise
- Dosedependent cytotoxicity leading to apoptosis or autophagy
- Transcriptional instability or inflammatory signalling activation (NF-κB, JNK, MAPK)
Use exclusively under controlled laboratory conditions with strict biosafety procedures.
Only GMP materials will be supplied, logistics all according to GDP.
Datasheet
| Molecular Formula | C29H38N4O6S |
|---|---|
| Molecular Weight | 570.7 g/mol |
| CAS Number | 54-35-3 |
| Storage Condition | Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light. |
| Solubility | Slightly soluble |
| Purity | Purity information is available upon request (COA). |
| Synonym | Procaine penicillin G; Procaine Benzylpenicillin; Depocillin; Duphapen; Hostacillin |
| IUPAC/Chemical Name | 2-(diethylamino)ethyl 4-aminobenzoate;(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid |
| InChl Key | WHRVRSCEWKLAHX-LQDWTQKMSA-N |
| InChl Code | InChI=1S/C16H18N2O4S.C13H20N2O2/c1-16(2)12(15(21)22)18-13(20)11(14(18)23-16)17-10(19)8-9-6-4-3-5-7-9;1-3-15(4-2)9-10-17-13(16)11-5-7-12(14)8-6-11/h3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22);5-8H,3-4,9-10,14H2,1-2H3/t11-,12+,14-;/m1./s1 |
| References |
3D Conformer.
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