Bioymifi

Modify Date: 2025-09-25 18:49:54

Bioymifi Structure
Bioymifi structure
Common Name Bioymifi
CAS Number 1420071-30-2 Molecular Weight 494.317
Density 1.8±0.1 g/cm3 Boiling Point N/A
Molecular Formula C22H12BrN3O4S Melting Point N/A
MSDS Chinese USA Flash Point N/A
Symbol GHS07
GHS07
Signal Word Warning

 Use of Bioymifi


Bioymifi(DR5 Activator) is the first novel and potent small-molecule activatior of the TRAIL receptor DR5 in human cancer cells.IC50 value:Target: In comparison with A2C2, bioymifi was able to promote cell death without the need for the Smac mimetic in T98G cells. Notably, at a 10-μM concentration, bioymifi induced processing of caspase-3 into smaller fragments. Z-VAD inhibited these caspase-mediated cleavages. caspase-3 was rapidly activated as early as 2 h after bioymifi treatment of T98G cells. The caspase-3 activity was markedly increased after 8 h of treatment. Bioymifi induces caspase-8–dependent apoptosis.

 Names

Name 5-(5-{(Z)-[3-(4-Bromophenyl)-2-imino-4-oxo-1,3-thiazolidin-5-ylidene]methyl}-2-furyl)-1H-isoindole-1,3(2H)-dione
Synonym More Synonyms

 Bioymifi Biological Activity

Description Bioymifi(DR5 Activator) is the first novel and potent small-molecule activatior of the TRAIL receptor DR5 in human cancer cells.IC50 value:Target: In comparison with A2C2, bioymifi was able to promote cell death without the need for the Smac mimetic in T98G cells. Notably, at a 10-μM concentration, bioymifi induced processing of caspase-3 into smaller fragments. Z-VAD inhibited these caspase-mediated cleavages. caspase-3 was rapidly activated as early as 2 h after bioymifi treatment of T98G cells. The caspase-3 activity was markedly increased after 8 h of treatment. Bioymifi induces caspase-8–dependent apoptosis.
Related Catalog
References

[1]. Wang G, et al. Small-molecule activation of the TRAIL receptor DR5 in human cancer cells. Nat Chem Biol. 2013 Feb;9(2):84-9.

 Chemical & Physical Properties

Density 1.8±0.1 g/cm3
Molecular Formula C22H12BrN3O4S
Molecular Weight 494.317
Exact Mass 492.973175
LogP 4.80
Appearance of Characters yellow solid
Index of Refraction 1.791
InChIKey ULBOWKXOFOTCMU-NLDKGBHCSA-N
SMILES N=C1SC(=Cc2ccc(-c3ccc4c(c3)C(=O)NC4=O)o2)C(=O)N1c1ccc(Br)cc1
Storage condition -20℃

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
RIDADR NONH for all modes of transport

 BioymifiBioassay

View more

Name: Diffuse intrinsic pontine glioma (SU-DIPG-XVII) cell line screen of MIPE5.0 library: ...
Source: 15316
Target: N/A
External Id: s-dipg-DIPG17_CTG48h_mipe5_0-1
Name: Diffuse intrinsic pontine glioma (SU-DIPG-XIII) cell line screen of MIPE4.0 library: ...
Source: 15316
Target: N/A
External Id: s-dipg-dipg13-1
Name: qHTS drug screen for cell cycle checkpoint inhibitors in PARPi-resistant BRCA-mutant ...
Source: NCGC
External Id: FGL-PARP_PEO-CTG96h-MIPE5.0-p1
Name: Diffuse intrinsic pontine glioma (JHH-DIPG-1) cell line screen of MIPE4.0 library: vi...
Source: 15316
Target: N/A
External Id: s-dipg-dipg1-1
Name: Diffuse intrinsic pontine glioma (SU-DIPG-IV) cell line screen of MIPE4.0 library: vi...
Source: 15316
Target: N/A
External Id: s-dipg-dipg4-1
Name: Diffuse intrinsic pontine glioma (SU-DIPG-XXV) cell line screen of MIPE5.0 library: v...
Source: 15316
Target: N/A
External Id: s-dipg-DIPG25-MIPE5.0-CTF48h-p1
Name: Cellular viability qHTS for adrenocortical cancer (ACC) cell line SW-13
Source: NCGC
Target: N/A
External Id: ACC-ATC-p1-SW13-72hr
Name: Cellular viability qHTS for adrenocortical cancer (ACC) cell line NCI-H295R
Source: NCGC
Target: N/A
External Id: ACC-ATC-p1-H295R-72hr
Name: Cytotoxicity counterscreen for inhibitors of SARS-CoV-2 cell entry
Source: NCGC
Target: N/A
External Id: TRND-SARS-CoV-2-cytotox-48hr
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 Synonyms

5-(5-{(Z)-[3-(4-Bromophenyl)-2-imino-4-oxo-1,3-thiazolidin-5-ylidene]methyl}-2-furyl)-1H-isoindole-1,3(2H)-dione
Bioymifi
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