FPH2

Modify Date: 2025-08-24 14:07:27

FPH2 Structure
FPH2 structure
Common Name FPH2
CAS Number 957485-64-2 Molecular Weight 353.82700
Density 1.45±0.1 g/cm3 Boiling Point N/A
Molecular Formula C14H16ClN5O2S Melting Point N/A
MSDS USA Flash Point N/A

 Use of FPH2


FPH2 induces of functional proliferation of primary human hepatocytes and may lead to the development of new therapeutics for liver diseases.

 Names

Name 1H-​Pyrazole-​3-​carboxamide, 4-​[[[(5-​chloro-​2-​methoxyphenyl)​amino]​thioxomethyl]​amino]​-​1-​ethyl
Synonym More Synonyms

 FPH2 Biological Activity

Description FPH2 induces of functional proliferation of primary human hepatocytes and may lead to the development of new therapeutics for liver diseases.
Related Catalog
In Vitro FPH2 induces functional proliferation of hepatocytes in vitro, and thus may be useful for expanding mature human primary hepatocytes. FPH1 and FPH2 can increase in hepatocyte nuclei count and/or elevate the number of nuclei undergoing mitosis during primary screening, and these effects on hepatocytes are concentration dependent. Cells treated with FPH1 and FPH2 also maintain their liver-specific functions. Over 7 days, FPH2 induces hepatocyte doublings at a rate that is consistent with reported liver regeneration kinetics in vivo[1].
References

[1]. Shan J, et al. Identification of small molecules for human hepatocyte expansion and iPS differentiation. Nat Chem Biol. 2013 Aug;9(8):514-20.

 Chemical & Physical Properties

Density 1.45±0.1 g/cm3
Molecular Formula C14H16ClN5O2S
Molecular Weight 353.82700
Exact Mass 353.07100
PSA 126.29000
LogP 3.31910
InChIKey PCHRYHSDDPPZBV-UHFFFAOYSA-N
SMILES CCn1cc(NC(=S)Nc2cc(Cl)ccc2OC)c(C(N)=O)n1
Storage condition -20℃
Water Solubility Practically insoluble (0.046 g/L) (25 ºC)

 Safety Information

RIDADR NONH for all modes of transport

 FPH2Bioassay

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Name: Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: ORF 73 [Human herpesvirus 8 type M]
External Id: HMS791
Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
Name: Primary qHTS for inhibitors of NSP2Pro chikungunya virus (CHIKV)
Source: NCGC
External Id: APP-Toga-CHIKV-nsp2-p
Name: High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS1303
Name: Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: HCMV UL50
External Id: HMS1262
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 Synonyms

FPH2
4-[[[(5-Chloro-2-methoxyphenyl)amino]thioxomethyl]amino]-1-ethyl-1H-pyrazole-3-carboxamide
BRD-9424
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