Golgicide A
Golgicide A (CAS: 1005036-73-6), with the molecular formula C17H14F2N2, is a specialised chemical compound. It is primarily utilised in biochemical research, particularly within the fields of cell biology, cell signalling, and neuroscience. Its applications extend to the study of G protein function and post-translational modifications, making it a valuable tool for researchers investigating complex biological pathways.
- IUPAC
- 6,8-Difluoro-4-pyridin-3-yl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline,CID 25113626,GCA

Cell Biology Research
Golgicide A is employed as a research chemical for investigating cellular processes. Its defined structure allows for precise studies into cellular mechanisms and signalling pathways.
Neuroscience and Cell Signalling
This compound serves as a probe in neuroscience and cell signalling research. It aids in understanding the intricate communication networks within cells and the nervous system.
G Protein Function Studies
Researchers utilise Golgicide A to explore the function of G proteins, crucial components in cellular signal transduction. Its specific interactions help elucidate these biochemical processes.
Post-translational Modification Analysis
Golgicide A can be used in the study of post-translational modifications, providing insights into how proteins are altered after synthesis and the impact on their function.
| Empirical formula | C17H14F2N2 |
|---|---|
| Assay | ≥98% (HPLC) |
| Solubility | DMSO: >10 mg/mL |
| Storage temperature | room temp |

Hazard statements
- H319Causes serious eye irritation
Precautionary statements
- P305IF IN EYES
| Water hazard class (WGK, DE) | 3 |
|---|
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Golgicide A primarily used for?
+
Golgicide A is primarily used in biochemical research, focusing on cell biology, cell signalling, neuroscience, G protein function, and post-translational modifications.
What is the CAS number and formula for Golgicide A?
+
The CAS number for Golgicide A is 1005036-73-6, and its molecular formula is C17H14F2N2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Golgicide A with a purity of ≥98% (HPLC). We do not represent this product as USP, BP, EP, or other pharmacopoeia grades unless explicitly stated in the product data.
How should Golgicide A be handled safely?
+
Golgicide A is classified with a GHS07 symbol and a Warning signal word, indicating it causes serious eye irritation (H319). Handle with appropriate personal protective equipment and follow P305 + P351 + P338 precautionary measures.
How is Golgicide A stored and shipped?
+
Golgicide A is typically stored at room temperature. TSS ensures appropriate packaging and shipping protocols for chemical compounds, adhering to international export regulations.
How can I request a sample or quote for Golgicide A?
+
To request a sample or a quote for Golgicide A, please contact our sales team via the website or direct email, providing your contact details and requested quantity.
▶ Related products

(−)-Curcumol
C15H24O2
Cell Biology
(±) Clopidogrel hydrogensulfate
Cell Biology

(±)-L-Alliin
C6H11NO3S
Cell Biology
(±)-2-Amino-4-phosphonobutyric acid
C4H10NO5P
Cell Biology
(±)-2-Methylarachidonoyl-2′-fluoroethylamide
C23H38NOF
Cell Biology
(±)-3,4-Methylenedioxy-N-ethylamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxyamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxymethamphetamine hydrochloride
Cell Biology
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis