u-73343

Base Information

Chemical Name:u-73343
CAS No.:142878-12-4
Molecular Formula:C29H42 N2 O3
Molecular Weight:466.66
Hs Code.:
European Community (EC) Number:634-320-2
UNII:S2C4J8704C
DSSTox Substance ID:DTXSID2036740
Nikkaji Number:J1.076.311H
Wikidata:Q27894098
ChEMBL ID:CHEMBL1628215
Mol file:142878-12-4.mol

Synonyms:1-(6-((17beta-3-methoxyestra-1,3,5(10)-triene-17-yl)amino)hexyl)-2,5-pyrrolidinedione;U 73343;U-73343

Suppliers and Price of u-73343

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
U 73343
10mg
$ 395.00

TRC
U-73343
2.5mg
$ 140.00

Tocris
U-73343 ≥98%(HPLC)
50
$ 682.00

Tocris
U-73343 ≥98%(HPLC)
10
$ 162.00

Sigma-Aldrich
U-73343
1mg
$ 140.00

Sigma-Aldrich
U-73343
5mg
$ 129.50

Sigma-Aldrich
U-73343
5mg
$ 200.00

ChemScene
U-73343 99.31%
5mg
$ 75.00

ChemScene
U-73343 99.31%
10mg
$ 125.00

ChemScene
U-73343 99.31%
50mg
$ 400.00

Total 13 raw suppliers

Chemical Property of u-73343

Chemical Property:

Vapor Pressure:2.37E-16mmHg at 25°C
Boiling Point:641.5°C at 760 mmHg
PKA:10.68±0.40(Predicted)
Flash Point:341.8°C
PSA：58.64000
Density:1.15g/cm³
LogP:5.54770
Storage Temp.:+15C to +30C
Solubility.:ethanol: 0.93 mg/mL
XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:9
Exact Mass:466.31954321
Heavy Atom Count:34
Complexity:725

Purity/Quality:

98%,99%, ^*data from raw suppliers

U 73343 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC12CCC3C(C1CCC2NCCCCCCN4C(=O)CCC4=O)CCC5=C3C=CC(=C5)OC
Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2NCCCCCCN4C(=O)CCC4=O)CCC5=C3C=CC(=C5)OC
Description U-73343 (142878-12-4) is a negative control for phospholipase C inhibitor U-73122 (Cat.# 10-1061).1,2 Elicits unexpected effects on rabbit parietal cells.3?Cell permeable.
Uses U-73343 is an inactive structural analog of U-73122.

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Technology Process of u-73343

u-73343

NAVIGATION