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Details

Stereochemistry ABSOLUTE
Molecular Formula C29H42N2O3
Molecular Weight 466.6554
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of U-73343

SMILES

[H][C@@]12CC[C@H](NCCCCCCN3C(=O)CCC3=O)[C@@]1(C)CC[C@]4([H])C5=C(CC[C@@]24[H])C=C(OC)C=C5

InChI

InChIKey=CJHWFIUASFBCKN-ZRJUGLEFSA-N
InChI=1S/C29H42N2O3/c1-29-16-15-23-22-10-8-21(34-2)19-20(22)7-9-24(23)25(29)11-12-26(29)30-17-5-3-4-6-18-31-27(32)13-14-28(31)33/h8,10,19,23-26,30H,3-7,9,11-18H2,1-2H3/t23-,24-,25+,26+,29+/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: GO:0004630 | phospholipase D activity
PubMed

PubMed

TitleDatePubMed
The putative phospholipase C inhibitor U73122 and its negative control, U73343, elicit unexpected effects on the rabbit parietal cell.
1997 Sep
U73122 and U73343 inhibit receptor-mediated phospholipase D activation downstream of phospholipase C in CHO cells.
1998 Apr 10
Inhibitory effects of U73122 and U73343 on Ca2+ influx and pore formation induced by the activation of P2X7 nucleotide receptors in mouse microglial cell line.
2005 Nov 15
Name Type Language
U-73343
Common Name English
1-(6-(((17.BETA.)-3-METHOXYESTRA-1,3,5(10)-TRIEN-17-YL)AMINO)HEXYL)-2,5-PYRROLIDINEDIONE
Systematic Name English
1-(6-((17BETA-3-METHOXYESTRA-1,3,5(10)-TRIEN-17-YL)-AMINO)HEXYL-2,5-PYRROLIDINE-DIONE
Common Name English
2,5-PYRROLIDINEDIONE, 1-(6-(((17.BETA.)-3-METHOXYESTRA-1,3,5(10)-TRIEN-17-YL)AMINO)HEXYL)-
Systematic Name English
Code System Code Type Description
FDA UNII
S2C4J8704C
Created by admin on Sat Dec 16 09:02:47 GMT 2023 , Edited by admin on Sat Dec 16 09:02:47 GMT 2023
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PUBCHEM
114825
Created by admin on Sat Dec 16 09:02:47 GMT 2023 , Edited by admin on Sat Dec 16 09:02:47 GMT 2023
PRIMARY
CAS
142878-12-4
Created by admin on Sat Dec 16 09:02:47 GMT 2023 , Edited by admin on Sat Dec 16 09:02:47 GMT 2023
PRIMARY
EPA CompTox
DTXSID2036740
Created by admin on Sat Dec 16 09:02:47 GMT 2023 , Edited by admin on Sat Dec 16 09:02:47 GMT 2023
PRIMARY