Saxagliptin Anhydrous

Saxagliptin Anhydrous

SCHEMBL8269188

N#CC1C[C@@H]2C[C@@H]2N1C(=O)C(N)C12CC3CC(CC(O)(C3)C1)C2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DPP4

The experimentally established mechanism targets of Saxagliptin Anhydrous. 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
▸ DPP4 known ✓ P27487 20/20 1.00
▸ CYP3A4 P08684 2/20 1.00
▸ DPP8 Q6V1X1 2/20 1.00
▸ DPP9 Q86TI2 2/20 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
Saxagliptin Anhydrous SCHEMBL988028 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL882684 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL17642049 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL988030 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL17168 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL23752173 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL8269720 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL14763515 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL1624269 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9
Saxagliptin Anhydrous SCHEMBL15579932 1.00 DPP4 (1.00) DPP4CYP3A4DPP8DPP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3315124-A1 BILAYER TABLET FORMULATIONS Astrazeneca AB (SE) 2018-05-02 — — EP disclosed
US-20120276600-A1 Process For Preparing Dipeptidyl Peptidase IV Inhibitors And Intermediates Therefor BRISTOL-MYERS SQUIBB COMPANY (US) 2012-11-01 — — US disclosed
EP-2505578-A2 Methods and Compounds for Producing Dipeptidyl Peptidase IV Inhibitors and Intermediates thereof Bristol-Myers Squibb Company (US) 2012-10-03 — — EP disclosed
EP-2505579-A2 Methods and compounds for producing dipeptidyl peptidase iv inhibitors and intermediates thereof Bristol-Myers Squibb Company (US) 2012-10-03 — — EP disclosed
US-8278462-B2 Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof BRISTOL-MYERS SQUIBB COMPANY (US) 2012-10-02 — — US disclosed
US-8222009-B2 Process for preparing dipeptidyl peptidase IV inhibitors and intermediates therefor BRISTOL-MYERS SQUIBB COMPANY (US) 2012-07-17 — — US disclosed
US-20100291642-A1 Process For Preparing Dipeptidyl Peptidase IV Inhibitors And Intermediates Therefor BRISTOL-MYERS SQUIBB COMPANY (US) 2010-11-18 — — US disclosed
US-20100274025-A1 METHODS AND COMPOUNDS FOR PRODUCING DIPEPTIDYL PEPTIDASE IV INHIBITORS AND INTERMEDIATES THEREOF BRISTOL-MYERS SQUIBB COMPANY (US) 2010-10-28 — — US disclosed
US-7741082-B2 Process for preparing dipeptidyl peptidase IV inhibitors and intermediates therefor BRISTOL-MYERS SQUIBB COMPANY (US) 2010-06-22 — — US disclosed
US-7705033-B2 Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof BRISTOL-MYERS SQUIBB COMPANY (US) 2010-04-27 — — US disclosed
US-7611880-B2 Enzymatic ammonolysis process for the preparation of intermediates for DPP IV inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2009-11-03 — — US disclosed
US-20090018311-A1 METHODS AND COMPOUNDS FOR PRODUCING DIPEPTIDYL PEPTIDASE IV INHIBITORS AND INTERMEDIATES THEREOF BRISTOL-MYERS SQUIBB COMPANY (US) 2009-01-15 — — US disclosed
US-7420079-B2 Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof BRISTOL-MYERS SQUIBB COMPANY (US) 2008-09-02 — — US disclosed
WO-2006020664-A2 AMMONOLYSIS PROCESS FOR THE PREPARATION OF INTERMEDIATES FOR DPP IV INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2006-02-23 — — WO disclosed
WO-2005115982-A1 PROCESS FOR PRODUCING A DIPEPTIDYL PEPTIDASE IV INHIBITOR BRISTOL-MYERS SQUIBB COMPANY (US) 2005-12-08 — — WO disclosed
WO-2005106011-A2 PROCESS FOR PREPARING DIPEPTIDYL IV INHIBITORS AND INTERMEDIATES THEREFOR BRISTOL-MYERS SQUIBB COMPANY (US) 2005-11-10 — — WO disclosed
US-20050222242-A1 Process for preparing a dipeptidyl peptidase IV inhibitor and intermediates employed therein ASTRAZENECA AB (SE) 2005-10-06 — — US disclosed
WO-2004052850-A2 METHODS AND COMPOUNDS PRODUCING DIPEPTIDYL PEPTIDASE IV INHIBITORS AND INTERMEDIATES THEREOF BRISTOL-MYERS SQUIBB COMPANY (US) 2004-06-24 — — 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 (4 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-20100274025-A1 METHODS AND COMPOUNDS FOR PRODUCING DIPEPTIDYL PEPTIDASE IV INHIBITORS AND INTERMEDIATES THEREOF DPP4, DPP3, DPP8 DPP4 1/4885CYP3A4 92/4885DPP8 3/4885
US-20050222242-A1 Process for preparing a dipeptidyl peptidase IV inhibitor and intermediates employed therein DPP4, DPP8, DPP7 DPP4 1/4885CYP3A4 130/4885DPP8 2/4885
US-20090018311-A1 METHODS AND COMPOUNDS FOR PRODUCING DIPEPTIDYL PEPTIDASE IV INHIBITORS AND INTERMEDIATES THEREOF DPP4, DPP3, DPP8 DPP4 1/4885CYP3A4 92/4885DPP8 3/4885
US-20120276600-A1 Process For Preparing Dipeptidyl Peptidase IV Inhibitors And Intermediates Therefor DNPEP, DPP4, DPP8 DPP4 2/4885CYP3A4 663/4885DPP8 3/4885

“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.

Send feedback