A proneurogenic and neuroprotective compound
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

P7C3

Item No. 16682

Technical Information
Formal Name
3,6-dibromo-α-[(phenylamino)methyl]-9H-carbazole-9-ethanol
CAS Number
301353-96-8
Molecular Formula
C21H18Br2N2O
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 0.2 mg/ml
λmax
235, 269, 305, 345, 360 nm
SMILES
BrC(C=C1)=CC2=C1N(CC(CNC3=CC=CC=C3)O)C4=CC=C(Br)C=C42
InChi Code
InChI=1S/C21H18Br2N2O/c22-14-6-8-20-18(10-14)19-11-15(23)7-9-21(19)25(20)13-17(26)12-24-16-4-2-1-3-5-16/h1-11,17,24,26H,12-13H2
InChi Key
FZHHRERIIVOATI-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Product Description

    P7C3 is an orally bioavailable and brain penetrant aminopropyl carbazole that exhibits proneurogenic and neuroprotective activity by preventing apoptosis of newly postmitotic neurons in the subgranular zone of the hippocampal dentate gyrus.1 At doses of 5 mg/kg and above, it has been shown to promote the survival of neurons in various rodent models of neurodegeneration or nerve injury.2,3 While the precise mechanism of action through which these effects are exerted remains uncertain, P7C3 recently has been shown to bind nicotinamide phosphoribosyltransferase, the rate-limiting enzyme involved in the conversion of nicotinamide into NAD.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Pieper, A.A., Xie, S., Capota, E., et alDiscovery of a pro-neurogenic, neuroprotective chemical. Cell 142(1), 39-51 (2010).

    2. De Jesús-Cortés, H., Xu, P., Drawbridge, J., et alNeuroprotective efficacy of aminopropyl carbazoles in a mouse model of Parkinson disease. Proc. Natl. Acad. Sci. USA 109(42), 17010-17015 (2012).

    3. Tesla, R., Wolf, H.P., Xu, P., et alNeuroprotective efficacy of aminopropyl carbazoles in a mouse model of amyotrophic lateral sclerosis. Proc. Natl. Acad. Sci. USA 109(42), 17016-17021 (2012).

    4. Wang, G., Han, T., Nijhawan, D., et alP7C3 neuroprotective chemicals function by activating the rate-limiting enzyme in NAD salvage. Cell 158(6), 1324-1334 (2014).