Valbenazine

Valbenazine

SCHEMBL871303

COc1cc2c(cc1OC)C1CC(OC(=O)[C@@H](N)C(C)C)C(CC(C)C)CN1CC2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC18A2

The experimentally established mechanism targets of Valbenazine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
SLC18A2 known ✓ Q05940 9/20 0.65
HTR1A P08908 1/20 1.00
TBXA2R P21731 1/20 1.00
PTGS1 P23219 1/20 1.00
OPRM1 P35372 1/20 1.00
KCNH2 Q12809 1/20 1.00
HTR2A P28223 1/20 0.65

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Valbenazine SCHEMBL17557525 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL17565511 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL15932979 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL23119371 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL872246 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL23771726 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL20049776 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL19024486 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL17565518 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2
Valbenazine SCHEMBL871304 1.00 HTR1A (1.00) HTR1ATBXA2RPTGS1OPRM1KCNH2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 39 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10919892-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) NEUROCRINE BIOSCIENCES, INC. (US) 2021-02-16 US claimed
US-10906902-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) NEUROCRINE BIOSCIENCES, INC. (US) 2021-02-02 US claimed
US-10906903-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) NEUROCRINE BIOSCIENCES, INC. (US) 2021-02-02 US claimed
US-20200347057-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) AGNO PHARMA USA 2020-11-05 US claimed
US-20200347055-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) NEUROCRINE BIOSCIENCES, INC. 2020-11-05 US claimed
US-20200347056-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) NEUROCRINE BIOSCIENCES, INC. 2020-11-05 US claimed
US-20200347054-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) NEUROCRINE BIOSCIENCES, INC. 2020-11-05 US claimed
EP-3394057-B1 SYNTHETIC METHOD FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]LSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) NEUROCRINE BIOSCIENCES INC (US) 2022-03-30 EP disclosed
US-20210087191-A1 SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-a]ISOQUINOLIN-2-OL COMPOUNDS, THEIR SYNTHESIS, AND USE THEREOF DISPERSOL TECHNOLOGIES, LLC 2021-03-25 US disclosed
US-10919892-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) NEUROCRINE BIOSCIENCES, INC. (US) 2021-02-16 US disclosed
US-10906902-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) NEUROCRINE BIOSCIENCES, INC. (US) 2021-02-02 US disclosed
US-10906903-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) NEUROCRINE BIOSCIENCES, INC. (US) 2021-02-02 US disclosed
US-20200347054-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) NEUROCRINE BIOSCIENCES, INC. 2020-11-05 US disclosed
US-8039627-B2 Substituted 3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-A]isoquinolin-2-ol compounds and methods relating thereto NEUROCRINE BIOSCIENCES, INC. (US) 2011-10-18 US disclosed
US-8039627-B2 Substituted 3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-A]isoquinolin-2-ol compounds and methods relating thereto NEUROCRINE BIOSCIENCES, INC. (US) 2011-10-18 US disclosed
US-8039627-B2 Substituted 3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-A]isoquinolin-2-ol compounds and methods relating thereto NEUROCRINE BIOSCIENCES, INC. (US) 2011-10-18 US disclosed
US-20080167337-A1 SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A]ISOQUINOLIN-2-OL COMPOUNDS AND METHODS RELATING THERETO NEUROCRINE BIOSCIENCES, INC. 2008-07-10 US disclosed
US-20080167337-A1 SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A]ISOQUINOLIN-2-OL COMPOUNDS AND METHODS RELATING THERETO NEUROCRINE BIOSCIENCES, INC. 2008-07-10 US disclosed
US-20080167337-A1 SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A]ISOQUINOLIN-2-OL COMPOUNDS AND METHODS RELATING THERETO NEUROCRINE BIOSCIENCES, INC. 2008-07-10 US disclosed
WO-2008058261-A1 SUBSTITUTED 3-ISOBUTYL-9, 10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A] ISOQUINOLIN-2-OL COMPOUNDS AND METHODS RELATING THERETO NEUROCRINE BIOSCIENCES, INC. (US) 2008-05-15 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (9 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20200347054-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) CYP2S1, CYP26B1, UGT2B7 SLC18A2 3816/4885HTR1A 202/4885TBXA2R 781/4885
US-20200347055-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) CYP2S1, CYP26B1, UGT2B7 SLC18A2 3816/4885HTR1A 202/4885TBXA2R 781/4885
US-20200347056-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) CYP2S1, CYP26B1, UGT2B7 SLC18A2 3816/4885HTR1A 202/4885TBXA2R 781/4885
US-20210087191-A1 SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-a]ISOQUINOLIN-2-OL COMPOUNDS, THEIR SYNTHESIS, AND USE THEREOF SLC6A2, SLC18A2, SLC6A3 SLC18A2 2/4885HTR1A 35/4885TBXA2R 831/4885
US-20080167337-A1 SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A]ISOQUINOLIN-2-OL COMPOUNDS AND METHODS RELATING THERETO SLC18A2, SLC6A2, SLC18A3 SLC18A2 1/4885HTR1A 85/4885TBXA2R 569/4885
US-20200347057-A1 SYNTHETIC METHODS FOR PREPARATION OF (S)-(2R,3R,11BR)-3-ISOBUTYL-9,10-DIMETHOXY-2,3,4,6,7,11B-HEXAHYDRO-1H-PYRIDO[2,1,-A]lSOQUINOLIN-2-YL 2-AMINO-3-METHYLBUTANOATE DI(4-METHYLBENZENESULFONATE) CYP2S1, CYP26B1, UGT2B7 SLC18A2 3816/4885HTR1A 202/4885TBXA2R 781/4885
US-10919892-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) CYP2S1, CYP26B1, CYP4B1 SLC18A2 3847/4885HTR1A 148/4885TBXA2R 1018/4885
US-10906903-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) CYP2S1, CYP26B1, CYP4B1 SLC18A2 3928/4885HTR1A 179/4885TBXA2R 1101/4885
US-10906902-B2 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) CYP2S1, CYP26B1, CYP4B1 SLC18A2 3708/4885HTR1A 138/4885TBXA2R 914/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.