SCHEMBL953788

SCHEMBL953788

CC(C)(C)OC(=O)N[C@@H](CCCO)C(=O)OCc1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
PPARA Q07869 2/20 0.55
CTSK P43235 4/20 0.55
KLK7 P49862 1/20 0.52
KLK5 Q9Y337 1/20 0.52
SYK P43405 1/20 0.52
CTSS P25774 4/20 0.52
MAPT P10636 1/20 0.51
PPARG P37231 1/20 0.50
CTSL P07711 1/20 0.50
CTSB P07858 1/20 0.50

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
SCHEMBL3906191 1.00 PPARA (0.55) PPARACTSKKLK7KLK5SYK
SCHEMBL693646 1.00 PPARA (0.55) PPARACTSKKLK7KLK5SYK
Alcohol SCHEMBL692835 0.98 CTSK (0.55) PPARACTSKKLK7KLK5SYK
SCHEMBL5970352 0.96 KLK7 (0.54) PPARACTSKKLK7KLK5SYK
SCHEMBL8615707 0.96 KLK7 (0.54) PPARACTSKKLK7KLK5SYK
SCHEMBL1094804 0.93 PPARA (0.57) PPARACTSKKLK7KLK5SYK
SCHEMBL13205156 0.93 PPARA (0.57) PPARACTSKKLK7KLK5SYK
SCHEMBL1094803 0.93 PPARA (0.57) PPARACTSKKLK7KLK5SYK
SCHEMBL7222412 0.90 SYK (0.55) PPARACTSKKLK7KLK5SYK
SCHEMBL5970655 0.90 SYK (0.55) PPARACTSKKLK7KLK5SYK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4720058-A2 BIFUNCTIONAL DEGRADERS AND USES THEREOF Casma Therapeutics, Inc. (US) 2026-04-08 EP disclosed
WO-2024249291-A2 BIFUNCTIONAL DEGRADERS AND USES THEREOF CASMA THERAPEUTICS, INC. (US) 2024-12-05 WO disclosed
US-9278997-B2 Processes for the manufacture of macrocyclic depsipeptides and new intermediates NOVARTIS AG (CH) 2016-03-08 US disclosed
US-9278997-B2 Processes for the manufacture of macrocyclic depsipeptides and new intermediates NOVARTIS AG (CH) 2016-03-08 US disclosed
US-20140080995-A1 Processes for the Manufacture of Macrocyclic Depsipeptides and New Intermediates NOVARTIS AG (CH) 2014-03-20 US disclosed
US-20140080995-A1 Processes for the Manufacture of Macrocyclic Depsipeptides and New Intermediates NOVARTIS AG (CH) 2014-03-20 US disclosed
US-8669266-B2 Quinoline-carboxamide derivatives as P2Y12 antagonists SANOFI (FR) 2014-03-11 US disclosed
US-8426420-B2 Heterocyclic pyrazole-carboxamidesas P2Y12 antagonists SANOFI (FR) 2013-04-23 US disclosed
US-20120277406-A1 Processes for the Manufacture of Macrocyclic Depsipeptides and New Intermediates NOVARTIS AG (CH) 2012-11-01 US disclosed
US-20120277406-A1 Processes for the Manufacture of Macrocyclic Depsipeptides and New Intermediates NOVARTIS AG (CH) 2012-11-01 US disclosed
US-7338947-B2 Cyclic derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB CO. (US) 2008-03-04 US disclosed
US-7183270-B2 Cyclic derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY (US) 2007-02-27 US disclosed
US-20070032541-A1 Cyclic derivatives as modulators of chemokine receptor activity CHERNEY ROBERT J 2007-02-08 US disclosed
EP-1606255-A4 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL MYERS SQUIBB CO (US) 2007-02-07 EP disclosed
EP-1606255-A2 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY Bristol-Myers Squibb Company (US) 2005-12-21 EP disclosed
US-20040186140-A1 Cyclic derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY 2004-09-23 US disclosed
WO-2004071460-A2 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL-MYERS SQUIBB COMPANY (US) 2004-08-26 WO disclosed
US-5710324-A AMINE CONTAINING COMPOUNDS MERRELL PHARMACEUTICALS INC. (US) 1998-01-20 US disclosed
US-5318992-A Administering for the treatment of hypotensive conditions and shock MERRELL DOW PHARMACEUTICALS INC. (US) 1994-06-07 US disclosed
EP-0446699-A1 Inhibitors of nitric oxide biosynthesis MERRELL PHARMACEUTICALS INC. (US) 1991-09-18 EP 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-20120277406-A1 Processes for the Manufacture of Macrocyclic Depsipeptides and New Intermediates VIP, NPPA, PTMS PPARA 4324/4885CTSK 1094/4885KLK7 1205/4885
US-20140080995-A1 Processes for the Manufacture of Macrocyclic Depsipeptides and New Intermediates VIP, NPPA, PTMS PPARA 4324/4885CTSK 1094/4885KLK7 1205/4885
US-20040186140-A1 Cyclic derivatives as modulators of chemokine receptor activity CCL11, CCR1, CCL2 PPARA 1474/4885CTSK 1779/4885KLK7 2664/4885
US-20070032541-A1 Cyclic derivatives as modulators of chemokine receptor activity CCL11, CCL2, CCR1 PPARA 1213/4885CTSK 1557/4885KLK7 2647/4885

“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.