Sotagliflozin

Sotagliflozin

SCHEMBL1038287

CCOc1ccc(Cc2cc([C@@H]3O[C@H](SC)[C@@H](O)[C@H](O)[C@H]3O)ccc2Cl)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC5A1SLC5A2

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
SLC5A1 known ✓ P13866 14/20 1.00
SLC5A2 known ✓ P31639 14/20 1.00
ADRA2A P08913 1/20 0.73
SLC5A11 Q8WWX8 1/20 0.73

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
Sotagliflozin SCHEMBL17036778 1.00 SLC5A1 (1.00) SLC5A1SLC5A2ADRA2ASLC5A11
Sotagliflozin SCHEMBL19512410 1.00 SLC5A1 (1.00) SLC5A1SLC5A2ADRA2ASLC5A11
Sotagliflozin SCHEMBL10267817 1.00 SLC5A1 (1.00) SLC5A1SLC5A2ADRA2ASLC5A11
Sotagliflozin SCHEMBL29433934 1.00 SLC5A1 (1.00) SLC5A1SLC5A2ADRA2ASLC5A11
Sotagliflozin SCHEMBL19853184 1.00 SLC5A1 (1.00) SLC5A1SLC5A2ADRA2ASLC5A11
Sotagliflozin SCHEMBL23731430 1.00 SLC5A1 (1.00) SLC5A1SLC5A2ADRA2ASLC5A11
SCHEMBL16234522 0.92 SLC5A2 (0.85) SLC5A1SLC5A2ADRA2ASLC5A11
SCHEMBL23077583 0.91 SLC5A1 (0.83) SLC5A1SLC5A2
SCHEMBL1036755 0.91 SLC5A2 (0.83) SLC5A1SLC5A2ADRA2ASLC5A11
SCHEMBL20787163 0.89 SLC5A1 (1.00) SLC5A1SLC5A2

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 1895 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4724042-A1 METHOD FOR IMPROVING THE INGESTION OF A LIQUID OR VISCOUS SUBSTANCE Ceva Santé Animale (FR) 2026-04-15 EP claimed
EP-4719430-A1 COMBINATION TREATMENT AND/OR PREVENTION OF RENAL DISEASES AND/OR HYPERTENSION IN NON-HUMAN MAMMALS COMPRISING ONE OR MORE SGLT-2 INHIBITORS AND TELMISARTAN Boehringer Ingelheim Vetmedica GmbH (DE) 2026-04-08 EP claimed
EP-4719429-A1 COMBINATION TREATMENT AND/OR PREVENTION OF CARDIAC DISEASES IN NON-HUMAN MAMMALS COMPRISING ONE OR MORE SGLT-2 INHIBITORS AND PIMOBENDAN AND/OR TELMISARTAN Boehringer Ingelheim Vetmedica GmbH (DE) 2026-04-08 EP claimed
US-20260076956-A1 METHODS FOR REGRESSING OR REVERSING FIBROSIS AND/OR LIVER CIRRHOSIS IN A SUBJECT IN NEED THEREOF USING HIGH-DOSE NIACIN, OR A NIACIN ANALOG THEREOF US GOV VETERANS AFFAIRS (US) 2026-03-19 US claimed
US-12577269-B2 Continuous process for preparing the crystalline form II of sotagliflozin LEXICON PHARMACEUTICALS, INC. (US) 2026-03-17 US claimed
US-20260069559-A1 COMBINATIONS OF RXFP1 MODULATORS AND SGLT2 INHIBITORS ASTRAZENECA AB (SE) 2026-03-12 US claimed
EP-4701626-A1 AMORPHOUS OBICETRAPIB AND SGLT2 INHIBITOR COMBINATION NewAmsterdam Pharma B.V. (NL) 2026-03-04 EP claimed
CN-121575079-A SGLT1/2 double-target inhibitor, screening method and application thereof, and diabetes treatment drug 广东药科大学 2026-02-27 CN claimed
US-12551484-B2 Methods of treatment and/or prevention of major adverse cardiovascular events (MACE) with a combination of a BET bromodomain inhibitor and a sodium dependent glucose transport 2 inhibitor RESVERLOGIX CORP. (CA) 2026-02-17 US claimed
EP-4691459-A1 COMBINATION FORMULATION COMPRISING SACUBITRIL-VALSARTAN AND SGLT-2 INHIBITOR HAVING IMPROVED STABILITY AND DISSOLUTION RATE Hanmi Pharm. Co., Ltd. (KR) 2026-02-11 EP claimed
US-8217156-B2 Solid forms of (2S,3R,4R,5S,6R)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-(methylthio)tetrahydro-2H-pyran-3,4,5-triol and methods of their use LEXICON PHARMACEUTICALS, INC. (US) 2012-07-10 US claimed
US-20120172320-A1 COMPOSITIONS COMPRISING AND METHODS OF USING INHIBITORS OF SODIUM-GLUCOSE COTRANSPORTERS 1 AND 2 PATHEON INC. (CA) 2012-07-05 US claimed
JP-2011528366-A 2011-11-17 JP claimed
WO-2011109333-A1 6 -BENZYLPHENYL- 2 - SULFURTERAHYDROPYRAN-3, 4, 5 -TRIOL DERIVATIVES AS INHIBITORS OF SODIUM -GLUCOSE COTRANS PORTERS 1 AND 2 FOR USE IN DIABETIC PATIENTS LEXICON PHARMACEUTICALS, INC. (US) 2011-09-09 WO claimed
US-20110218159-A1 METHODS OF USING INHIBITORS OF SODIUM-GLUCOSE COTRANSPORTERS 1 AND 2 LEXICON PHARMACEUTICALS, INC. 2011-09-08 US claimed
US-20110077212-A1 THERAPEUTIC USES OF SGLT2 INHIBITORS THERACOS, INC. (US) 2011-03-31 US claimed
EP-2089361-B1 INHIBITORS OF SODIUM GLUCOSE CO-TRANSPORTER 2 AND METHODS OF THEIR USE LEXICON PHARMACEUTICALS INC (US) 2011-01-26 EP claimed
US-7781577-B2 2-[4-Chloro-3-(4-hydroxy-benzyl)-phenyl]-6-methoxy-tetrahydro-pyran-3,4,5-triol; 2-[4-Chloro-3-(4-ethoxy-benzyl)-phenyl]-3,4,5-trihydroxy-piperidine-1-carboxylic acid methyl ester; (2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-methoxytetrahydro-2H-thiopyran-3,4,5-triol; antidibetic, antiobesity agents LEXICON PHARMACEUTICALS, INC. (US) 2010-08-24 US claimed
WO-2010009197-A1 SOLID FORMS OF (2S,3R,4R,5S,6R)-2-(4-CHLORO-3-(4-ETHOXYBENZYL)PHENYL)-6-(METHYLTHIO)TETRAHYDRO-2H-PYRAN-3,4,5-TRIOL AND METHODS OF THEIR USE LEXICON PHARMACEUTICALS, INC. (US) 2010-01-21 WO claimed
US-20100016422-A1 SOLID FORMS OF (2S,3R,4R,5S,6R)-2-(4-CHLORO-3-(4-ETHOXYBENZYL)PHENYL)-6-(METHYLTHIO)TETRAHYDRO-2H-PYRAN-3,4,5-TRIOL AND METHODS OF THEIR USE OXFORD FINANCE LLC, AS COLLATERAL AGENT 2010-01-21 US claimed

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

For each of this compound's patents that has machine-readable text (8 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-20260069559-A1 COMBINATIONS OF RXFP1 MODULATORS AND SGLT2 INHIBITORS RXFP1, RXFP2, RXFP4 SLC5A1 5/4885SLC5A2 6/4885ADRA2A 617/4885
US-20120172320-A1 COMPOSITIONS COMPRISING AND METHODS OF USING INHIBITORS OF SODIUM-GLUCOSE COTRANSPORTERS 1 AND 2 SLC5A2, SLC5A1, SLC2A2 SLC5A1 2/4885SLC5A2 1/4885ADRA2A 557/4885
US-20110077212-A1 THERAPEUTIC USES OF SGLT2 INHIBITORS SLC5A2, SLC5A1, PPARG SLC5A1 2/4885SLC5A2 1/4885ADRA2A 157/4885
US-20100016422-A1 SOLID FORMS OF (2S,3R,4R,5S,6R)-2-(4-CHLORO-3-(4-ETHOXYBENZYL)PHENYL)-6-(METHYLTHIO)TETRAHYDRO-2H-PYRAN-3,4,5-TRIOL AND METHODS OF THEIR USE TPMT, PYGL, PNPO SLC5A1 354/4885SLC5A2 233/4885ADRA2A 2928/4885
US-20260076956-A1 METHODS FOR REGRESSING OR REVERSING FIBROSIS AND/OR LIVER CIRRHOSIS IN A SUBJECT IN NEED THEREOF USING HIGH-DOSE NIACIN, OR A NIACIN ANALOG THEREOF COL1A1, COL2A1, FN1 SLC5A1 551/4885SLC5A2 669/4885ADRA2A 1254/4885
US-12551484-B2 Methods of treatment and/or prevention of major adverse cardiovascular events (MACE) with a combination of a BET bromodomain inhibitor and a sodium dependent glucose transport 2 inhibitor SLC5A2, SLC5A1, BRD4 SLC5A1 2/4885SLC5A2 1/4885ADRA2A 858/4885
US-12577269-B2 Continuous process for preparing the crystalline form II of sotagliflozin SLC5A2, SLC5A1, GCK SLC5A1 2/4885SLC5A2 1/4885ADRA2A 539/4885
US-20110218159-A1 METHODS OF USING INHIBITORS OF SODIUM-GLUCOSE COTRANSPORTERS 1 AND 2 SLC5A2, SLC5A1, SLC2A2 SLC5A1 2/4885SLC5A2 1/4885ADRA2A 457/4885

“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.