307543-71-1,MFCD02332975
Catalog No.:AA00BF1Y

307543-71-1 | STF 083010

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$6.00   $4.00
- +
5mg
98%
in stock  
$12.00   $8.00
- +
10mg
98%
in stock  
$22.00   $16.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00BF1Y
Chemical Name:
STF 083010
CAS Number:
307543-71-1
Molecular Formula:
C15H11NO3S2
Molecular Weight:
317.3827
MDL Number:
MFCD02332975
SMILES:
O=C1C=Cc2c(/C/1=C/NS(=O)(=O)c1cccs1)cccc2
Properties
Computed Properties
 
Complexity:
486  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
1  
Formal Charge:
0  
Heavy Atom Count:
21  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
3.7  

Upstream Synthesis Route

[1]Patent:WO2014/176348,2014,A1,.Locationinpatent:Page/Pagecolumn51;52

Downstream Synthesis Route

[1]Patent:WO2014/176348,2014,A1.Locationinpatent:Page/Pagecolumn51;52

Literature

Title: Gap junctional intercellular communication and endoplasmic reticulum stress regulate chronic cadmium exposure induced apoptosis in HK-2 cells.

Journal: Toxicology letters 20180515

Title: Papandreou I, et al. Identification of an Ire1alpha endonuclease specific inhibitor with cytotoxic activity against human multiple myeloma. Blood. 2011 Jan 27;117(4):1311-4.

Title: Chien W, et al. Selective inhibition of unfolded protein response induces apoptosis in pancreatic cancer cells. Oncotarget. 2014 Jul 15;5(13):4881-94.

Title: Namba T, et al. Loss of p53 enhances the function of the endoplasmic reticulum through activation of the IRE1α/XBP1 pathway. Oncotarget. 2015 Aug 21;6(24):19990-20001.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 307543-71-1
Historical Records
Tags:307543-71-1 Molecular Formula|307543-71-1 MDL|307543-71-1 SMILES|307543-71-1 STF 083010
Catalog No.: AA00BF1Y
307543-71-1,MFCD02332975
307543-71-1 | STF 083010
Pack Size: 1mg
Purity: 98%
in stock
$6.00 $4.00
Pack Size: 5mg
Purity: 98%
in stock
$12.00 $8.00
Pack Size: 10mg
Purity: 98%
in stock
$22.00 $16.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00BF1Y
Chemical Name: STF 083010
CAS Number: 307543-71-1
Molecular Formula: C15H11NO3S2
Molecular Weight: 317.3827
MDL Number: MFCD02332975
SMILES: O=C1C=Cc2c(/C/1=C/NS(=O)(=O)c1cccs1)cccc2
Properties
Complexity: 486  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 1  
Formal Charge: 0  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 3.7  
Upstream Synthesis Route
6339-87-3    708-06-5    307543-71-1 

[1]Patent:WO2014/176348,2014,A1,.Locationinpatent:Page/Pagecolumn51;52

Downstream Synthesis Route
6339-87-3    708-06-5    307543-71-1 

[1]Patent:WO2014/176348,2014,A1.Locationinpatent:Page/Pagecolumn51;52

Literature fold

Title: Gap junctional intercellular communication and endoplasmic reticulum stress regulate chronic cadmium exposure induced apoptosis in HK-2 cells.

Journal: Toxicology letters20180515

Title: Papandreou I, et al. Identification of an Ire1alpha endonuclease specific inhibitor with cytotoxic activity against human multiple myeloma. Blood. 2011 Jan 27;117(4):1311-4.

Title: Chien W, et al. Selective inhibition of unfolded protein response induces apoptosis in pancreatic cancer cells. Oncotarget. 2014 Jul 15;5(13):4881-94.

Title: Namba T, et al. Loss of p53 enhances the function of the endoplasmic reticulum through activation of the IRE1α/XBP1 pathway. Oncotarget. 2015 Aug 21;6(24):19990-20001.

Building Blocks More >
21744-83-2
21744-83-2
2-Methyl-1,4-benzoxazin-3-one
AA00BF63 | MFCD04141926
2538-87-6
2538-87-6
3-(4-Hydroxyphenyl)acrylaldehyde
AA00BFCL | MFCD00599378
28140-37-6
28140-37-6
1,2-O-(1-Ethoxyethylidene)-beta-d-mannopyranose triacetate
AA00BFK5 | MFCD01863564
220731-04-4
220731-04-4
tert-Butyl 5-aminopyridin-2-ylcarbamate
AA00BG17 | MFCD25948963
218157-81-4
218157-81-4
6-(1H-Pyrrol-1-yl)nicotinonitrile
AA00BGDL | MFCD00828638
3002-77-5
3002-77-5
2-Methyl-1,10-phenanthroline
AA00BGU4 | MFCD06643855
309713-15-3
309713-15-3
Ethyl 2-amino-4-(4-chlorophenyl)-1H-pyrrole-3-carboxylate
AA00BGYD | MFCD00244763
268729-12-0
268729-12-0
Fmoc-o-tert-butyl-d-trans-4-hydroxyproline
AA00BHGO | MFCD00798649
3105-97-3
3105-97-3
1-((2-(Diethylamino)ethyl)amino)-4-(hydroxymethyl)-9H-thioxanthen-9-one
AA00BHRK | MFCD00083383
2856-79-3
2856-79-3
Benzeneacetic acid, .alpha.-broMo-2-chloro-, ethyl ester
AA00BI36 | MFCD18429752
Submit
© 2017 AA BLOCKS, INC. All rights reserved.