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Details

Stereochemistry RACEMIC
Molecular Formula C28H36O7
Molecular Weight 484.5812
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SC-41930

SMILES

CCCC1=C(OC)C(=CC=C1OCCCOC2=CC=C3CCC(OC3=C2CCC)C(O)=O)C(C)=O

InChI

InChIKey=ZVVCSBSDFGYRCB-UHFFFAOYSA-N
InChI=1S/C28H36O7/c1-5-8-21-23(13-10-19-11-14-25(28(30)31)35-26(19)21)33-16-7-17-34-24-15-12-20(18(3)29)27(32-4)22(24)9-6-2/h10,12-13,15,25H,5-9,11,14,16-17H2,1-4H3,(H,30,31)

HIDE SMILES / InChI

Molecular Formula C28H36O7
Molecular Weight 484.5812
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

SC-41930 has been shown to be a specific LTB4 receptor antagonist both in vitro and in vivo. SC-41930 can produce significant anti-inflammatory effects. The anti-inflammatory activity of SC-41930 could be attributed to postreceptor inhibition of inflammatory mediator production by human neutrophil and other cells in addition to antagonism of human neutrophil LTB4 receptors.

Approval Year

PubMed

PubMed

TitleDatePubMed
In vivo characterization of zymosan-induced mouse peritoneal inflammation.
1994 Jun
Phorbol ester-induced dermal inflammation in mice: evaluation of inhibitors of 5-lipoxygenase and antagonists of leukotriene B4 receptor.
1994 Sep
Blockade of human neutrophil activation by 2-[2-propyl-3-[3-[2-ethyl-4-(4-fluorophenyl)-5- hydroxyphenoxy]propoxy]phenoxy]benzoic acid (LY293111), a novel leukotriene B4 receptor antagonist.
1995 May 26
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: mice data
1 mg/kg pretriatment (-30 min) before 6-trans-LTB4 injection
Route of Administration: Oral
In Vitro Use Guide
SC-41930 was evaluated for effects on human neutrophil chemotaxis and degranulation. At concentrations up to 100 uM, SC-41930 alone exhibited no effect on neutrophil migration, but dose-dependently inhibited neutrophil chemotaxis induced by leukotriene B4 (LTB4) in a modified Boyden chamber. Concentrations of SC-41930 from 0.3 uM to 3 uM competitively inhibited LTB4-induced chemotaxis with a pA2 value of 6.35.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:52:12 GMT 2023
Edited
by admin
on Fri Dec 15 15:52:12 GMT 2023
Record UNII
EVH7O0422T
Record Status Validated (UNII)
Record Version
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Name Type Language
SC-41930
Common Name English
(±)-7-(3-(4-ACETYL-3-METHOXY-2-PROPYLPHENOXY)PROPOXY)-3,4-DIHYDRO-8-PROPYL-2H-1-BENZOPYRAN-2-CARBOXYLIC ACID
Systematic Name English
2H-1-BENZOPYRAN-2-CARBOXYLIC ACID, 7-(3-(4-ACETYL-3-METHOXY-2-PROPYLPHENOXY)PROPOXY)-3,4-DIHYDRO-8-PROPYL-
Common Name English
7-(3-(4-ACETYL-3-METHOXY-2-PROPYL-PHENOXY)PROPOXYL-3,4-DIHYDRO-8-PROPYL-2H-1-BENZOPYRAN-2-CARBOXYLIC ACID
Common Name English
CGS-24115
Code English
Classification Tree Code System Code
FDA ORPHAN DRUG 164102
Created by admin on Fri Dec 15 15:52:12 GMT 2023 , Edited by admin on Fri Dec 15 15:52:12 GMT 2023
Code System Code Type Description
FDA UNII
EVH7O0422T
Created by admin on Fri Dec 15 15:52:12 GMT 2023 , Edited by admin on Fri Dec 15 15:52:12 GMT 2023
PRIMARY
PUBCHEM
114999
Created by admin on Fri Dec 15 15:52:12 GMT 2023 , Edited by admin on Fri Dec 15 15:52:12 GMT 2023
PRIMARY
CAS
120072-59-5
Created by admin on Fri Dec 15 15:52:12 GMT 2023 , Edited by admin on Fri Dec 15 15:52:12 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY