Canagliflozin Anhydrous

Canagliflozin Anhydrous

SCHEMBL16421559

Cc1ccc([C@@H]2OC(CO)[C@@H](O)[C@H](O)C2O)cc1Cc1ccc(-c2ccc(F)cc2)s1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC5A2

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

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
SLC5A2 known ✓ P31639 20/20 1.00
SLC5A1 P13866 6/20 1.00
ABCB11 O95342 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
SLC6A4 P31645 1/20 1.00
SLC6A3 Q01959 1/20 1.00

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
Canagliflozin Anhydrous SCHEMBL19293442 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL157162 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL16075101 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL19493514 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL873848 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL19493519 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL24037935 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL13695263 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL15888791 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4
Canagliflozin Anhydrous SCHEMBL19293553 1.00 SLC5A2 (1.00) SLC5A2SLC5A1ABCB11ADORA3SLC6A4

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170247359-A1 PROCESS FOR THE PREPARATION OF CANAGLIFLOZIN MYLAN LABORATORIES LTD (IN) 2017-08-31 US disclosed
US-20170247359-A1 PROCESS FOR THE PREPARATION OF CANAGLIFLOZIN MYLAN LABORATORIES LTD (IN) 2017-08-31 US disclosed
US-20160250221-A1 INHIBITORS OF FAPP2 AND USES THEREOF FONDAZIONE TELETHON (IT) 2016-09-01 US disclosed
US-20160250221-A1 INHIBITORS OF FAPP2 AND USES THEREOF FONDAZIONE TELETHON (IT) 2016-09-01 US disclosed
WO-2016041530-A1 COMPLEXES OF CANAGLIFLOZIN AND CYCLODEXTRINS ZENTIVA, K.S. (CZ) 2016-03-24 WO disclosed
WO-2015011284-A2 INHIBITORS OF FAPP2 AND USES THEREOF FONDAZIONE TELETHON (IT) 2015-01-29 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 (2 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-20160250221-A1 INHIBITORS OF FAPP2 AND USES THEREOF GBA2, GBA1, ACER2 SLC5A2 2100/4885SLC5A1 3068/4885ABCB11 4187/4885
US-20170247359-A1 PROCESS FOR THE PREPARATION OF CANAGLIFLOZIN SLC5A2, SLC5A1, SLC2A4 SLC5A2 1/4885SLC5A1 2/4885ABCB11 665/4885

“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.