STAT3 inhibitor
CHEBI:CHEBI_87183
Definition
An inhibitor of signal transducer and activator of transcription 3 (STAT3)
Alternative Names
- signal transducer and activator of transcription 3 inhibitor
- signal transducer and activator of transcription 3 inhibitors
- STAT3 inhibitors
Treatment Applications
-
severe congenital neutropenia 8View Disease →
DOID:0112135
-
severe congenital neutropenia 4View Disease →
DOID:0112136
-
spermatogenic failure 52View Disease →
DOID:0112270
-
spermatogenic failure 51View Disease →
DOID:0112273
-
X-linked spermatogenic failure 3View Disease →
DOID:0112274
-
pontocerebellar hypoplasia type 1FView Disease →
DOID:0112331
-
spermatogenic failure 54View Disease →
DOID:0112335
-
spermatogenic failure 56View Disease →
DOID:0112336
-
spermatogenic failure 57View Disease →
DOID:0112338
-
spermatogenic failure 61View Disease →
DOID:0112350
-
spermatogenic failure 62View Disease →
DOID:0112351
-
spermatogenic failure 58View Disease →
DOID:0112352
-
spermatogenic failure 65View Disease →
DOID:0112354
-
spermatogenic failure 63View Disease →
DOID:0112356
-
spermatogenic failure 59View Disease →
DOID:0112357
-
spondylocostal dysostosis 3View Disease →
DOID:0112361
-
spondylocostal dysostosis 2View Disease →
DOID:0112362
-
spondylocostal dysostosis 1View Disease →
DOID:0112365
-
Coffin-Siris syndrome 8View Disease →
DOID:0112367
-
Coffin-Siris syndrome 7View Disease →
DOID:0112369
-
Coffin-Siris syndrome 12View Disease →
DOID:0112370
-
Coffin-Siris syndrome 10View Disease →
DOID:0112371
-
Coffin-Siris syndrome 11View Disease →
DOID:0112372
-
juvenile spinal muscular atrophyView Disease →
DOID:12376
-
Werdnig-Hoffmann diseaseView Disease →
DOID:13137
-
Machado-Joseph diseaseView Disease →
DOID:1440
-
adult spinal muscular atrophyView Disease →
DOID:0050529
-
pseudo-TORCH syndrome 1View Disease →
DOID:0050656
-
X-linked severe combined immunodeficiencyView Disease →
DOID:0060013
-
MASA syndromeView Disease →
DOID:0060246
-
lethal congenital contracture syndrome 1View Disease →
DOID:0060559
-
sclerosteosis 1View Disease →
DOID:0060756
-
patterned macular dystrophy 3View Disease →
DOID:0060865
-
facioscapulohumeral muscular dystrophy 3View Disease →
DOID:0060917
-
facioscapulohumeral muscular dystrophy 4View Disease →
DOID:0060918
-
Seckel syndrome 9View Disease →
DOID:0070005
-
Seckel syndrome 6View Disease →
DOID:0070006
-
Seckel syndrome 1View Disease →
DOID:0070007
-
Seckel syndrome 10View Disease →
DOID:0070008
-
Seckel syndrome 8View Disease →
DOID:0070009
-
Seckel syndrome 4View Disease →
DOID:0070010
-
Seckel syndrome 7View Disease →
DOID:0070011
-
Seckel syndrome 5View Disease →
DOID:0070012
-
Seckel syndrome 2View Disease →
DOID:0070013
-
Coffin-Siris syndrome 1View Disease →
DOID:0070042
-
Coffin-Siris syndrome 3View Disease →
DOID:0070045
-
Coffin-Siris syndrome 4View Disease →
DOID:0070046
-
Meckel syndrome 3View Disease →
DOID:0070117
-
Meckel syndrome 4View Disease →
DOID:0070118
-
Meckel syndrome 5View Disease →
DOID:0070119
-
Meckel syndrome 6View Disease →
DOID:0070120
-
Meckel syndrome 7View Disease →
DOID:0070121
-
Meckel syndrome 8View Disease →
DOID:0070122
-
autosomal dominant cutis laxa 1View Disease →
DOID:0070130
-
autosomal recessive cutis laxa type ICView Disease →
DOID:0070139
-
hereditary sensory neuropathy type 1FView Disease →
DOID:0070154
-
hereditary sensory neuropathy type 1DView Disease →
DOID:0070156
-
hereditary sensory neuropathy type 1EView Disease →
DOID:0070158
-
spermatogenic failure 2View Disease →
DOID:0070164
-
spermatogenic failure 18View Disease →
DOID:0070165
-
spermatogenic failure 6View Disease →
DOID:0070167
-
spermatogenic failure 3View Disease →
DOID:0070168
-
spermatogenic failure 8View Disease →
DOID:0070169
-
spermatogenic failure 12View Disease →
DOID:0070171
-
spermatogenic failure 15View Disease →
DOID:0070172
-
spermatogenic failure 7View Disease →
DOID:0070173
-
spermatogenic failure 17View Disease →
DOID:0070174
-
spermatogenic failure 4View Disease →
DOID:0070176
-
spermatogenic failure 10View Disease →
DOID:0070178
-
spermatogenic failure 14View Disease →
DOID:0070179
-
spermatogenic failure 11View Disease →
DOID:0070180
-
spermatogenic failure 23View Disease →
DOID:0070181
-
spermatogenic failure 13View Disease →
DOID:0070182
-
spermatogenic failure 16View Disease →
DOID:0070184
-
X-linked spermatogenic failure 2View Disease →
DOID:0070185
-
Y-linked spermatogenic failure 1View Disease →
DOID:0070186
-
Y-linked spermatogenic failure 2View Disease →
DOID:0070187
-
spermatogenic failure 1View Disease →
DOID:0070188
-
X-linked spermatogenic failure 1View Disease →
DOID:0070189
-
Loeys-Dietz syndrome 4View Disease →
DOID:0070233
-
primary autosomal recessive microcephaly 7View Disease →
DOID:0070278
-
primary autosomal recessive microcephaly 5View Disease →
DOID:0070280
-
primary autosomal recessive microcephaly 8View Disease →
DOID:0070282
-
primary autosomal recessive microcephaly 1View Disease →
DOID:0070285
-
primary autosomal recessive microcephaly 3View Disease →
DOID:0070286
-
primary autosomal recessive microcephaly 9View Disease →
DOID:0070292
-
multiple epiphyseal dysplasia 7View Disease →
DOID:0070302
-
diphthamide deficiency syndrome 1View Disease →
DOID:0070477
-
diphthamide deficiency syndrome 2View Disease →
DOID:0070478
-
schwannomatosis 1View Disease →
DOID:0070480
-
schwannomatosis 2View Disease →
DOID:0070481
-
aortic valve disease 2View Disease →
DOID:0080334
-
ST2 diffuse large B-cell lymphomaView Disease →
DOID:0081068
-
split hand-foot malformation 1View Disease →
DOID:0090021
-
split hand-foot malformation 5View Disease →
DOID:0090022
-
split hand-foot malformation 4View Disease →
DOID:0090023
-
split hand-foot malformation 3View Disease →
DOID:0090025
-
split hand-foot malformation 6View Disease →
DOID:0090026
-
split hand-foot malformation 2View Disease →
DOID:0090027
-
cortical dysplasia-focal epilepsy syndromeView Disease →
DOID:0090130
-
achromatopsia 3View Disease →
DOID:0110008
-
achromatopsia 7View Disease →
DOID:0110009
-
achromatopsia 4View Disease →
DOID:0110010
-
age related macular degeneration 10View Disease →
DOID:0110022
-
age related macular degeneration 11View Disease →
DOID:0110023
-
age related macular degeneration 13View Disease →
DOID:0110025
-
asphyxiating thoracic dystrophy 1View Disease →
DOID:0110085
-
asphyxiating thoracic dystrophy 2View Disease →
DOID:0110086
-
asphyxiating thoracic dystrophy 3View Disease →
DOID:0110087
-
asphyxiating thoracic dystrophy 4View Disease →
DOID:0110088
-
asphyxiating thoracic dystrophy 5View Disease →
DOID:0110089
-
atopic dermatitis 4View Disease →
DOID:0110100
-
atopic dermatitis 6View Disease →
DOID:0110102
-
atopic dermatitis 7View Disease →
DOID:0110103
-
atopic dermatitis 8View Disease →
DOID:0110104
-
atopic dermatitis 9View Disease →
DOID:0110105
-
atrial heart septal defect 1View Disease →
DOID:0110106
-
Bartter disease type 4bView Disease →
DOID:0110146
-
Charcot-Marie-Tooth disease type 1CView Disease →
DOID:0110151
-
Charcot-Marie-Tooth disease type 2A1View Disease →
DOID:0110154
-
dilated cardiomyopathy 1HHView Disease →
DOID:0110448
-
long QT syndrome 3View Disease →
DOID:0110646
-
long QT syndrome 11View Disease →
DOID:0110652
-
Oguchi disease-1View Disease →
DOID:0110712
-
Oguchi disease-2View Disease →
DOID:0110713
-
congenital stationary night blindness 1GView Disease →
DOID:0110714
-
hereditary spastic paraplegia 10View Disease →
DOID:0110763
-
hereditary spastic paraplegia 13View Disease →
DOID:0110766
-
hereditary spastic paraplegia 3AView Disease →
DOID:0110791
-
hereditary spastic paraplegia 4View Disease →
DOID:0110792
-
Usher syndrome type 1FView Disease →
DOID:0110832
-
Usher syndrome type 1KView Disease →
DOID:0110837
-
Usher syndrome type 3BView Disease →
DOID:0110842
-
congenital stationary night blindness 1FView Disease →
DOID:0110864
-
congenital stationary night blindness 1BView Disease →
DOID:0110865
-
congenital stationary night blindness 1HView Disease →
DOID:0110866
-
congenital stationary night blindness 1CView Disease →
DOID:0110867
-
congenital stationary night blindness 1DView Disease →
DOID:0110868
-
congenital stationary night blindness 1EView Disease →
DOID:0110869
-
congenital stationary night blindness 1AView Disease →
DOID:0110870
-
hereditary spherocytosis type 1View Disease →
DOID:0110916
-
hereditary spherocytosis type 2View Disease →
DOID:0110917
-
hereditary spherocytosis type 3View Disease →
DOID:0110918
-
hereditary spherocytosis type 4View Disease →
DOID:0110919
-
hereditary spherocytosis type 5View Disease →
DOID:0110920
-
autosomal dominant sensory ataxia 1View Disease →
DOID:0111170
-
familial hemiplegic migraine 1View Disease →
DOID:0111181
-
familial hemiplegic migraine 3View Disease →
DOID:0111183
-
facioscapulohumeral muscular dystrophy 1View Disease →
DOID:0111192
-
facioscapulohumeral muscular dystrophy 2View Disease →
DOID:0111193
-
centronuclear myopathy 5View Disease →
DOID:0111222
-
centronuclear myopathy 4View Disease →
DOID:0111224
-
vestibular schwannomatosisView Disease →
DOID:0111252
-
restrictive cardiomyopathy 1View Disease →
DOID:0111425
-
restrictive cardiomyopathy 3View Disease →
DOID:0111427
-
Li-Fraumeni syndrome 1View Disease →
DOID:0111503
-
dehydrated hereditary stomatocytosis 1View Disease →
DOID:0111576
-
ectodermal dysplasia 11BView Disease →
DOID:0111654
-
ectodermal dysplasia 6View Disease →
DOID:0111659
-
ectodermal dysplasia 10BView Disease →
DOID:0111665
-
X-linked deafness 5View Disease →
DOID:0111741
-
cerebellar ataxia type 47View Disease →
DOID:0111743
-
syndactyly type 1View Disease →
DOID:0111816
-
syndactyly type 3View Disease →
DOID:0111817
-
syndactyly type 4View Disease →
DOID:0111818
-
X-linked spinocerebellar ataxia 1View Disease →
DOID:0111829
-
X-linked spinocerebellar ataxia 2View Disease →
DOID:0111830
-
X-linked spinocerebellar ataxia 3View Disease →
DOID:0111831
-
X-linked spinocerebellar ataxia 4View Disease →
DOID:0111832
-
X-linked spinocerebellar ataxia 5View Disease →
DOID:0111833
-
spermatogenic failure 30View Disease →
DOID:0111913
-
spermatogenic failure 35View Disease →
DOID:0111914
-
spermatogenic failure 33View Disease →
DOID:0111915
-
spermatogenic failure 28View Disease →
DOID:0111916
-
spermatogenic failure 25View Disease →
DOID:0111920
-
spermatogenic failure 36View Disease →
DOID:0111921
-
spermatogenic failure 31View Disease →
DOID:0111922
-
spermatogenic failure 42View Disease →
DOID:0111923
-
spermatogenic failure 26View Disease →
DOID:0111924
-
spermatogenic failure 32View Disease →
DOID:0111925
-
spermatogenic failure 39View Disease →
DOID:0111926
-
immunodeficiency 31BView Disease →
DOID:0111944
-
immunodeficiency 31AView Disease →
DOID:0111945
-
immunodeficiency 36View Disease →
DOID:0111949
-
immunodeficiency 10View Disease →
DOID:0111970
-
Sotos syndrome 1View Disease →
DOID:0112103
-
severe congenital neutropenia 7View Disease →
DOID:0112129
-
severe congenital neutropenia 2View Disease →
DOID:0112131
-
severe congenital neutropenia 5View Disease →
DOID:0112132
-
severe congenital neutropenia 3View Disease →
DOID:0112133
-
severe congenital neutropenia 6View Disease →
DOID:0112134
Drug Classification
-
inhibitorView Class →
CHEBI:35222
-
biochemical roleView Class →
CHEBI:52206
Important Medical Information
⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.
- Always consult with a healthcare professional before starting, stopping, or modifying any medication.
- Side effects may vary and this list may not be comprehensive.
- Drug interactions may occur with other medications.
Additional Identifiers
- core#notation
- CHEBI:87183
- oboInOwl#hasDbXref
- Wikipedia:STAT3
Additional References
🔍 Click on any linked disease name to learn more about the conditions this medication is used to treat, or explore related drug classifications for more information about similar medications.
Additional Attributes
- oboInOwl#hasOBONamespace
- chebi_ontology
- oboInOwl#id
- CHEBI:87183
- core#notation
- CHEBI:87183
- oboInOwl#hasDbXref
- Wikipedia:STAT3
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/chebi#3_STAR
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#range
- https://w3id.org/def/predibionto#has_drug_106644
- RO_0000087
- http://purl.obolibrary.org/obo/CHEBI_7553
- owl#someValuesFrom
- t286809
- owl#annotatedSource
- t314319