venetoclax
CHEBI:CHEBI_133021
Definition
A member of the class of pyrrolopyridines that is a potent inhibitor of the antiapoptotic protein B-cell lymphoma 2. It is used for treamtment of chronic lymphocytic leukemia with 17p deletion.
Chemical Information
- Molecular Formula
- C45H50ClN7O7S
- Molecular Mass
- 868.442
- Charge
- 0
- SMILES
- C1N(CCN(C1)C2=CC=C(C(NS(C3=CC=C(C(=C3)[N+](=O)[O-])NCC4CCOCC4)(=O)=O)=O)C(=C2)OC=5C=C6C(=NC5)NC=C6)CC=7CCC(CC7C=8C=CC(=CC8)Cl)(C)C
- InChI
- InChI=1S/C45H50ClN7O7S/c1-45(2)15-11-33(39(26-45)31-3-5-34(46)6-4-31)29-51-17-19-52(20-18-51)35-7-9-38(42(24-35)60-36-23-32-12-16-47-43(32)49-28-36)44(54)50-61(57,58)37-8-10-40(41(25-37)53(55)56)48-27-30-13-21-59-22-14-30/h3-10,12,16,23-25,28,30,48H,11,13-15,17-22,26-27,29H2,1-2H3,(H,47,49)(H,50,54)
- InChIKey
- LQBVNQSMGBZMKD-UHFFFAOYSA-N
Alternative Names
- 4-{4-[(4'-chloro-5,5-dimethyl[3,4,5,6-tetrahydro[1,1'-biphenyl]]-2-yl)methyl]piperazin-1-yl}-N-(3-nitro-4-{[(oxan-4-yl)methyl]amino}benzene-1-sulfonyl)-2-[(1H-pyrrolo[2,3-b]pyridin-5-yl)oxy]benzamide
- ABT 199
- ABT-199
- ABT199
- GDC 0199
- Venclexta
- venetoclax
Treatment Applications
-
pemphigus gestationisView Disease →
DOID:0040098
-
Frasier syndromeView Disease →
DOID:0050438
-
mantle cell lymphomaView Disease →
DOID:0050746
-
janus kinase-3 deficiencyView Disease →
DOID:0060008
-
recombinase activating gene 1 deficiencyView Disease →
DOID:0060011
-
recombinase activating gene 2 deficiencyView Disease →
DOID:0060012
-
CD3epsilon deficiencyView Disease →
DOID:0060017
-
CD3gamma deficiencyView Disease →
DOID:0060018
-
DNA ligase IV deficiencyView Disease →
DOID:0060021
-
CD40 ligand deficiencyView Disease →
DOID:0060022
-
immunoglobulin alpha deficiencyView Disease →
DOID:0060025
-
acute promyelocytic leukemiaView Disease →
DOID:0060318
-
Galloway-Mowat syndrome 1View Disease →
DOID:0060364
-
chromosome 10q23 deletion syndromeView Disease →
DOID:0060389
-
distal 10q deletion syndromeView Disease →
DOID:0060390
-
chromosome 15q24 deletion syndromeView Disease →
DOID:0060395
-
chromosome 16p12.1 deletion syndromeView Disease →
DOID:0060399
-
chromosome 17p13.1 deletion syndromeView Disease →
DOID:0060402
-
chromosome 17q11.2 deletion syndromeView Disease →
DOID:0060403
-
chromosome 17q12 deletion syndromeView Disease →
DOID:0060404
-
chromosome 17q23.1-q23.2 deletion syndromeView Disease →
DOID:0060405
-
chromosome 18p deletion syndromeView Disease →
DOID:0060406
-
chromosome 1p36 deletion syndromeView Disease →
DOID:0060410
-
chromosome 1q41-q42 deletion syndromeView Disease →
DOID:0060412
-
chromosome 2p12-p11.2 deletion syndromeView Disease →
DOID:0060414
-
chromosome 2q31.2 deletion syndromeView Disease →
DOID:0060416
-
3p deletion syndromeView Disease →
DOID:0060417
-
chromosome 3q13.31 deletion syndromeView Disease →
DOID:0060418
-
chromosome 3q29 microdeletion syndromeView Disease →
DOID:0060419
-
chromosome 4q21 deletion syndromeView Disease →
DOID:0060420
-
chromosome 5q12 deletion syndromeView Disease →
DOID:0060421
-
chromosome 6pter-p24 deletion syndromeView Disease →
DOID:0060422
-
chromosome 6q24-q25 deletion syndromeView Disease →
DOID:0060424
-
chromosome 8q21.11 deletion syndromeView Disease →
DOID:0060425
-
SATB2-associated syndromeView Disease →
DOID:0060428
-
chromosome 16p13.3 duplication syndromeView Disease →
DOID:0060431
-
chromosome 17p13.3 duplication syndromeView Disease →
DOID:0060432
-
chromosome 17q12 duplication syndromeView Disease →
DOID:0060433
-
chromosome 17q21.31 duplication syndromeView Disease →
DOID:0060434
-
Hermansky-Pudlak syndrome 2View Disease →
DOID:0060540
-
Hermansky-Pudlak syndrome 4View Disease →
DOID:0060542
-
Hermansky-Pudlak syndrome 7View Disease →
DOID:0060545
-
Hermansky-Pudlak syndrome 8View Disease →
DOID:0060546
-
3MC syndrome 2View Disease →
DOID:0060576
-
cerebral cavernous malformation 3View Disease →
DOID:0060671
-
X-linked lymphoproliferative syndrome 1View Disease →
DOID:0060705
-
X-linked lymphoproliferative syndrome 2View Disease →
DOID:0060706
-
lymphoproliferative syndrome 1View Disease →
DOID:0060707
-
lymphoproliferative syndrome 2View Disease →
DOID:0060708
-
Smith-Magenis syndromeView Disease →
DOID:0060768
-
Potocki-Lupski syndromeView Disease →
DOID:0060853
-
obsolete Koolen-De Vries syndromeView Disease →
DOID:0070076
-
obsolete Noonan syndrome 3View Disease →
DOID:0070103
-
obsolete Noonan syndrome 10View Disease →
DOID:0070110
-
childhood acute myeloid leukemiaView Disease →
DOID:0070323
-
microcephaly and chorioretinopathy 2View Disease →
DOID:0080106
-
chronic neutrophilic leukemiaView Disease →
DOID:0080187
-
syndromic X-linked mental retardation 35View Disease →
DOID:0080241
-
orofaciodigital syndrome XVIView Disease →
DOID:0080254
-
Joubert syndrome 29View Disease →
DOID:0080276
-
Joubert syndrome 33View Disease →
DOID:0080279
-
obsolete X-linked recessive diseaseView Disease →
DOID:0080341
-
blepharocheilodontic syndrome 1View Disease →
DOID:0080345
-
Meier-Gorlin syndrome 5View Disease →
DOID:0080516
-
agammaglobulinemia 5View Disease →
DOID:0080588
-
alopecia-mental retardation syndrome 2View Disease →
DOID:0080629
-
B-lymphoblastic leukemia/lymphomaView Disease →
DOID:0080630
-
B-cell acute lymphoblastic leukemiaView Disease →
DOID:0080638
-
medulloblastoma non-WNT/non-SHH group 4View Disease →
DOID:0080708
-
Fanconi renotubular syndrome 2View Disease →
DOID:0080758
-
plasmablastic lymphomaView Disease →
DOID:0080779
-
childhood acute megakaryoblastic leukemiaView Disease →
DOID:0080794
-
core binding factor acute myeloid leukemiaView Disease →
DOID:0080796
-
acute myeloid leukemiaView Disease →
DOID:9119
-
chromosome 2q37 deletion syndromeView Disease →
DOID:0111704
-
immunodeficiency 16View Disease →
DOID:0111935
-
immunodeficiency 22View Disease →
DOID:0111937
-
immunodeficiency 24View Disease →
DOID:0111938
-
immunodeficiency 37View Disease →
DOID:0111939
-
immunodeficiency 46View Disease →
DOID:0111948
-
immunodeficiency 11AView Disease →
DOID:0111957
-
immunodeficiency 15BView Disease →
DOID:0111959
-
immunodeficiency 15AView Disease →
DOID:0111960
-
immunodeficiency 26View Disease →
DOID:0111961
-
immunodeficiency 19View Disease →
DOID:0111972
-
immunodeficiency 17View Disease →
DOID:0111973
-
immunodeficiency 49View Disease →
DOID:0111979
-
immunodeficiency 64View Disease →
DOID:0111980
-
immunodeficiency 56View Disease →
DOID:0111982
-
immunodeficiency 53View Disease →
DOID:0111992
-
immunodeficiency 61View Disease →
DOID:0111999
-
X-linked dyserythropoietic anemiaView Disease →
DOID:0112156
-
focal segmental glomerulosclerosis 3View Disease →
DOID:0112245
-
brain small vessel disease 3View Disease →
DOID:0112315
-
pontocerebellar hypoplasia type 16View Disease →
DOID:0112333
-
prolymphocytic leukemiaView Disease →
DOID:1039
-
acute biphenotypic leukemiaView Disease →
DOID:9953
-
chronic lymphocytic leukemiaView Disease →
DOID:1040
-
Cri-Du-Chat syndromeView Disease →
DOID:12580
-
X-linked agammaglobulinemiaView Disease →
DOID:14179
-
Down syndromeView Disease →
DOID:14250
-
Rubinstein-Taybi syndromeView Disease →
DOID:1933
-
monoclonal paraproteinemiaView Disease →
DOID:2346
-
myxoid liposarcomaView Disease →
DOID:5363
-
plasma cell leukemiaView Disease →
DOID:9513
-
Pelger-Huet anomalyView Disease →
DOID:9631
-
null-cell leukemiaView Disease →
DOID:9954
-
cranioectodermal dysplasia 2View Disease →
DOID:0080804
-
cranioectodermal dysplasia 3View Disease →
DOID:0080805
-
cranioectodermal dysplasia 4View Disease →
DOID:0080806
-
mammary analogue secretory carcinomaView Disease →
DOID:0080808
-
pericytoma with t(7;12)View Disease →
DOID:0080896
-
astroblastoma, MN1-alteredView Disease →
DOID:0080904
-
alopecia-mental retardation syndrome 4View Disease →
DOID:0080950
-
acute myeloid leukemia with BCR-ABL1View Disease →
DOID:0080976
-
Cowden syndrome 5View Disease →
DOID:0081001
-
mixed phenotype acute leukemia, B/myeloidView Disease →
DOID:0081038
-
mixed phenotype acute leukemia, T/myeloidView Disease →
DOID:0081039
-
B-cell prolymphocytic leukemiaView Disease →
DOID:0081041
-
frontonasal dysplasia 3View Disease →
DOID:0081047
-
BN2 diffuse large B-cell lymphomaView Disease →
DOID:0081064
-
EZB diffuse large B-cell lymphomaView Disease →
DOID:0081065
-
MCD diffuse large B-cell lymphomaView Disease →
DOID:0081066
-
A53 diffuse large B-cell lymphomaView Disease →
DOID:0081069
-
EZB-MYC+ diffuse large B-cell lymphomaView Disease →
DOID:0081070
-
EZB-MYC- diffuse large B-cell lymphomaView Disease →
DOID:0081071
-
acute promyelocytic leukemia with PML-RARAView Disease →
DOID:0081081
-
acute myeloid leukemia with mutated NPM1View Disease →
DOID:0081089
-
acute myeloid leukemia with mutated RUNX1View Disease →
DOID:0081091
-
acute myeloid leukemia with mutated CEBPAView Disease →
DOID:0081095
-
Baraitser-Winter syndrome 2View Disease →
DOID:0081113
-
agammaglobulinemia 2View Disease →
DOID:0081135
-
agammaglobulinemia 3View Disease →
DOID:0081137
-
agammaglobulinemia 6View Disease →
DOID:0081138
-
agammaglobulinemia 7View Disease →
DOID:0081139
-
agammaglobulinemia 8AView Disease →
DOID:0081140
-
agammaglobulinemia 9View Disease →
DOID:0081141
-
agammaglobulinemia 8BView Disease →
DOID:0081143
-
common variable immunodeficiency 2View Disease →
DOID:0081145
-
common variable immunodeficiency 3View Disease →
DOID:0081146
-
common variable immunodeficiency 4View Disease →
DOID:0081147
-
common variable immunodeficiency 5View Disease →
DOID:0081148
-
common variable immunodeficiency 6View Disease →
DOID:0081149
-
common variable immunodeficiency 7View Disease →
DOID:0081150
-
common variable immunodeficiency 8View Disease →
DOID:0081151
-
common variable immunodeficiency 11View Disease →
DOID:0081153
-
common variable immunodeficiency 13View Disease →
DOID:0081155
-
common variable immunodeficiency 14View Disease →
DOID:0081156
-
acromesomelic dysplasia-3View Disease →
DOID:0081237
-
EWSR1-negative small round cell tumorView Disease →
DOID:0081249
-
pulmonary venoocclusive disease 1View Disease →
DOID:0081268
-
embryonal tumor with multilayered rosettesView Disease →
DOID:0081286
-
grade I lymphomatoid granulomatosisView Disease →
DOID:0081308
-
chromosome 5q deletion syndromeView Disease →
DOID:0090016
-
hereditary neutrophiliaView Disease →
DOID:0090120
-
Bardet-Biedl syndrome 9View Disease →
DOID:0110131
-
Charcot-Marie-Tooth disease axonal type 2XView Disease →
DOID:0110176
-
dilated cardiomyopathy 1WView Disease →
DOID:0110446
-
Warburg micro syndrome 2View Disease →
DOID:0110717
-
hereditary spastic paraplegia 34View Disease →
DOID:0110785
-
Usher syndrome type 1GView Disease →
DOID:0110834
-
Usher syndrome type 1JView Disease →
DOID:0110836
-
Joubert syndrome 27View Disease →
DOID:0110996
-
Joubert syndrome 7View Disease →
DOID:0111002
-
familial hypobetalipoproteinemia 1View Disease →
DOID:0111062
-
angioimmunoblastic T-cell lymphomaView Disease →
DOID:0111147
-
Ruijs-Aalfs syndromeView Disease →
DOID:0111264
Drug Classification
-
N-arylpiperazineView Class →
CHEBI:46848
-
N-sulfonylcarboxamideView Class →
CHEBI:90852
-
aromatic etherView Class →
CHEBI:35618
-
N-alkylpiperazineView Class →
CHEBI:46845
-
monochlorobenzenesView Class →
CHEBI:83403
-
C-nitro compoundView Class →
CHEBI:35716
-
pyrrolopyridineView Class →
CHEBI:46771
-
oxanesView Class →
CHEBI:46942
-
t99715
-
t99762
-
t100583
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
- DRON_00010000
- 1747556
- oboInOwl#hasDbXref
- Wikipedia:Venetoclax
- core#notation
- CHEBI:133021
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
- rdf-schema#range
- https://w3id.org/def/predibionto#has_drug_113895
- oboInOwl#hasOBONamespace
- chebi_ontology
- DRON_00010000
- 1747556
- oboInOwl#hasDbXref
- Wikipedia:Venetoclax
- oboInOwl#id
- CHEBI:133021
- core#notation
- CHEBI:133021
- RO_0000087
- http://purl.obolibrary.org/obo/CHEBI_68495
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/chebi#3_STAR
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- has_treatment
- http://purl.obolibrary.org/obo/DOID_0081412
- owl#annotatedSource
- t100692
- owl#someValuesFrom
- t3003361
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_side_effect1981