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  • DC Chemicals Limited
  • China
  • Product Name: P7C3
  • Price: $375.0/100mg $750.0/250mg $1500.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

301353-96-8

301353-96-8 structure
301353-96-8 structure
  • Name: P7C3
  • Chemical Name: 1-anilino-3-(3,6-dibromocarbazol-9-yl)propan-2-ol
  • CAS Number: 301353-96-8
  • Molecular Formula: C21H18Br2N2O
  • Molecular Weight: 474.188
  • Catalog: Signaling Pathways Metabolic Enzyme/Protease Nampt
  • Create Date: 2016-04-19 05:38:53
  • Modify Date: 2024-01-04 07:30:07
  • P7C3 is a NAMPT activator. P7C3 can enhance learning and memory in aged rats. Protects newborn neurons in the dentate gyrus by mitigating cell death. In vitro: Administration of active P7C3 chemicals to cells treated with doxorubicin, which induces NAD depletion, led to a rebound in intracellular levels of NAD and concomitant protection from doxorubicin-mediated toxicity. In vivo: P7C3 is orally bioavailable, crosses the blood-brain barrier, and is non-toxic at doses several fold higher than the efficacious dose.An easily administered pro-neurogenic compound. The administration of P7C3 is 10mg/ kg( IP) in rats. Administration of P7C3 to normal mice, as well as npas3-/- mice, enhance survival of neurons subsequent to their birth in the SGZ.

Name 1-anilino-3-(3,6-dibromocarbazol-9-yl)propan-2-ol
Synonyms P7C3
1-(3,6-Dibromo-carbazol-9-yl)-3-phenylamino-propan-2-ol
1-Anilino-3-(3,6-dibromo-9H-carbazol-9-yl)-2-propanol
9H-Carbazole-9-ethanol, 3,6-dibromo-α-[(phenylamino)methyl]-
1-(3,6-dibromo-9H-carbazol-9-yl)-3-(phenylamino)propan-2-ol
1-Anilino-3-(3,6-dibromo-9H-carbazol-9-yl)propan-2-ol
Description P7C3 is a NAMPT activator. P7C3 can enhance learning and memory in aged rats. Protects newborn neurons in the dentate gyrus by mitigating cell death. In vitro: Administration of active P7C3 chemicals to cells treated with doxorubicin, which induces NAD depletion, led to a rebound in intracellular levels of NAD and concomitant protection from doxorubicin-mediated toxicity. In vivo: P7C3 is orally bioavailable, crosses the blood-brain barrier, and is non-toxic at doses several fold higher than the efficacious dose.An easily administered pro-neurogenic compound. The administration of P7C3 is 10mg/ kg( IP) in rats. Administration of P7C3 to normal mice, as well as npas3-/- mice, enhance survival of neurons subsequent to their birth in the SGZ.
Related Catalog
References

[1]. Pieper AA et al. Discovery of a proneurogenic, neuroprotective chemical. Cell. 2010 Jul 9;142(1):39-51.

[2]. Wang G et al. P7C3 neuroprotective chemicals function by activating the rate-limiting enzyme in NAD salvage. Cell. 2014 Sep 11;158(6):1324-34.

[3]. Pieper AA et al. P7C3 and an unbiased approach to drug discovery for neurodegenerative diseases. Chem Soc Rev. 2014 Oct 7;43(19):6716-26.

Density 1.6±0.1 g/cm3
Boiling Point 656.4±55.0 °C at 760 mmHg
Molecular Formula C21H18Br2N2O
Molecular Weight 474.188
Flash Point 350.8±31.5 °C
Exact Mass 471.978577
PSA 37.19000
LogP 6.60
Appearance white solid
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.687
Storage condition -20℃
Symbol GHS05 GHS06
GHS05, GHS06
Signal Word Danger
Hazard Statements H301-H318
Precautionary Statements P280-P301 + P310-P305 + P351 + P338
RIDADR UN 2811 6.1 / PGIII
HS Code 2933990090
HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%