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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H28N4O3
Molecular Weight 468.5469
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RUBOXISTAURIN

SMILES

CN(C)C[C@@H]1CCN2C=C(C3=C2C=CC=C3)C4=C(C(=O)NC4=O)C5=CN(CCO1)C6=C5C=CC=C6

InChI

InChIKey=ZCBUQCWBWNUWSU-SFHVURJKSA-N
InChI=1S/C28H28N4O3/c1-30(2)15-18-11-12-31-16-21(19-7-3-5-9-23(19)31)25-26(28(34)29-27(25)33)22-17-32(13-14-35-18)24-10-6-4-8-20(22)24/h3-10,16-18H,11-15H2,1-2H3,(H,29,33,34)/t18-/m0/s1

HIDE SMILES / InChI

Description
Curator's Comment: The description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/23404115 | https://www.ncbi.nlm.nih.gov/pubmed/19825373 | https://www.ncbi.nlm.nih.gov/pubmed/15380221

Ruboxistaurin is an orally bioavailable, selective, potent inhibitor of protein kinase C β developed for treating diabetic retinopathy. In vitro and in vivo non-clinical models have demonstrated that Ruboxistaurin decreases PKC β activity and ameliorates many of the effects of PKC β on pathologic processes in the retina. Ruboxistaurin prevents the slowing of retinal blood flow that is observed by fluorescein video angiography in the eyes of diabetic rats. It is also reported to cause regression of retinal neovascularization produced by laser-induced major branch vein occlusions in a porcine model. Ruboxistaurin positively affected the diabetes-induced retinal blood flow abnormalities in a Phase Ib study in diabetic patients. Ruboxistaurin is in phase III clinical trials for the treatment of diabetic nephropathy and diabetic macular edema. Eli Lilly had submitted Ruboxistaurin for approval in the US and the EU; however, the company subsequently discontinued development as it was unable to demonstrate sufficient efficacy

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
5.9 nM [IC50]
360.0 nM [IC50]
300.0 nM [IC50]
52.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Synthesis of anilino-monoindolylmaleimides as potent and selective PKCbeta inhibitors.
2004 Oct 18
Docetaxel Facilitates Endothelial Dysfunction through Oxidative Stress via Modulation of Protein Kinase C Beta: The Protective Effects of Sotrastaurin.
2015 May
Patents

Patents

Sample Use Guides

32 mg/day
Route of Administration: Oral
HUVECs co-cultured with fibroblasts were cultivated in the presence or absence of various concentrations of ruboxistaurin (0.1 and 1 mkM) plus VEGF (10 ng/ml) at days 1, 4, 7 and 9. The ruboxistaurin was dissolved in dimethyl sulfoxide (DMSO, final concentration of DMSO was 0.1%). DMSO (0.1%) was added to the non-drug control (control group). At day 11, cells were fixed in 70% ethanol. The cells were incubated with diluted primary antibody (mouse anti-human CD31, 1 : 4000) for 1 h at 37 C, and with the secondary antibody (goat anti-mouse IgG alkaline phosphataseconjugated antibody, 1 : 500) for 1 h at 37 C. Visualization was achieved using 5-bromo-4-chloro-3-indolyl phosphate/nitro blue tetrazolium.
Name Type Language
RUBOXISTAURIN
INN   MART.   MI   VANDF   WHO-DD  
INN  
Official Name English
Ruboxistaurin [WHO-DD]
Common Name English
RUBOXISTAURIN [MI]
Common Name English
ruboxistaurin [INN]
Common Name English
RUBOXISTAURIN [VANDF]
Common Name English
RUBOXISTAURIN [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2089
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
Code System Code Type Description
WIKIPEDIA
RUBOXISTAURIN
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY
NCI_THESAURUS
C66524
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY
PUBCHEM
153999
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY
FDA UNII
721809WQCP
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY
DRUG CENTRAL
3533
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY
MERCK INDEX
m9693
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY Merck Index
MESH
C099154
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY
INN
8108
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
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EPA CompTox
DTXSID00168775
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
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ChEMBL
CHEMBL91829
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
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CAS
169939-94-0
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
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DRUG BANK
DB11829
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
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SMS_ID
100000089175
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
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EVMPD
SUB25202
Created by admin on Fri Dec 15 16:26:37 GMT 2023 , Edited by admin on Fri Dec 15 16:26:37 GMT 2023
PRIMARY