SCHEMBL820518

SCHEMBL820518

O=C(O)[C@@H]1[C@@H](O)CCN1C(=O)OCc1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.58
NPC1 O15118 1/20 0.58
RAB9A P51151 1/20 0.58
CYP2C19 P33261 1/20 0.52
AGTR2 P50052 5/20 0.51
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
NPSR1 Q6W5P4 1/20 0.49
F2 P00734 2/20 0.48
ELANE P08246 2/20 0.48
CTSG P08311 1/20 0.48
PREP P48147 1/20 0.48

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
SCHEMBL29613583 1.00 SMN1; SMN2 (0.58) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
SCHEMBL21874593 1.00 SMN1; SMN2 (0.58) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
SCHEMBL4920606 1.00 SMN1; SMN2 (0.58) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
SCHEMBL818735 1.00 SMN1; SMN2 (0.58) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
SCHEMBL16857371 0.93 SMN1; SMN2 (0.54) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL19234258 0.93 SMN1; SMN2 (0.53) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
SCHEMBL19592114 0.93 SMN1; SMN2 (0.53) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
SCHEMBL2678862 0.93 SMN1; SMN2 (0.53) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
Hydrochloric Acid SCHEMBL5409774 0.92 SMN1; SMN2 (0.52) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2
SCHEMBL13547241 0.91 SMN1; SMN2 (0.59) SMN1; SMN2NPC1RAB9ACYP2C19AGTR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4727552-A2 PASSIVE PERMEABLE PCSK9 ANTAGONIST COMPOUNDS Merck Sharp & Dohme LLC (US) 2026-04-22 EP disclosed
EP-4660303-A2 PCSK9 ANTAGONIST COMPOUNDS Merck Sharp & Dohme LLC (US) 2025-12-10 EP disclosed
EP-3810626-B1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC (US) 2025-07-23 EP disclosed
US-20250206781-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC (US) 2025-06-26 US disclosed
US-12209145-B2 PCSK9 antagonist compounds MERCK SHARP & DOHME LLC (US) 2025-01-28 US disclosed
WO-2024259310-A2 PASSIVE PERMEABLE PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC (US) 2024-12-19 WO disclosed
US-20230165932-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC 2023-06-01 US disclosed
US-20230165932-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC 2023-06-01 US disclosed
US-20230159592-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC 2023-05-25 US disclosed
US-20230159592-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC 2023-05-25 US disclosed
US-20100009957-A1 NOVEL INHIBITORS OF BETA-LACTAMASE MERCK SHARP & DOHME CORP. 2010-01-14 US disclosed
US-20100004441-A1 N-(5-Membered Aromatic Ring)-Amido Anti-Viral Compounds SCHMITZ FRANZ ULRICH 2010-01-07 US disclosed
US-7595398-B2 N-(5-membered aromatic ring)-amido anti-viral compounds SMITHKLINE BEECHAM CORPORATION (US) 2009-09-29 US disclosed
WO-2009094287-A1 IAP INHIBITORS TETRALOGIC PHARMACEUTICAL CORPORATION (US) 2009-07-30 WO disclosed
EP-1971597-A2 N-(5-MEMBERED HETEROAROMATIC RING)-AMIDO ANTI-VIRAL COMPOUNDS GENELABS TECHNOLOGIES, INC. (US) 2008-09-24 EP disclosed
US-20070265265-A1 N-(5-MEMBERED AROMATIC RING)-AMIDO ANTI-VIRAL COMPOUNDS GENELABS TECHNOLOGIES, INC. 2007-11-15 US disclosed
WO-2007070600-A2 N-(5-MEMBERED HETEROAROMATIC RING)-AMIDO ANTI-VIRAL COMPOUNDS GENELABS TECHNOLOGIES, INC. (US) 2007-06-21 WO disclosed
EP-1237862-A1 SUCCINATE COMPOUNDS, COMPOSITIONS AND METHODS OF USE AND PREPARATION Versicor, Inc. (US) 2002-09-11 EP disclosed
WO-2001044179-A1 NOVEL SUCCINATE COMPOUNDS, COMPOSITIONS AND METHODS OF USE AND PREPARATION VERSICOR, INC. (US) 2001-06-21 WO disclosed
EP-0533516-B1 Amides of 1-(alkoxybenzyl)piperazines, processes for their preparation and pharmaceutical compositions containing them ADIR (FR) 1995-02-08 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 (7 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-20100009957-A1 NOVEL INHIBITORS OF BETA-LACTAMASE MGAM, SI, MGAM2 SMN1; SMN2 3397/4885NPC1 2149/4885RAB9A 1833/4885
US-20230165932-A1 PCSK9 ANTAGONIST COMPOUNDS PCSK9, PCSK7, PCSK6 SMN1; SMN2 3778/4885NPC1 82/4885RAB9A 1128/4885
US-20230159592-A1 PCSK9 ANTAGONIST COMPOUNDS PCSK9, PCSK7, PCSK6 SMN1; SMN2 4322/4885NPC1 121/4885RAB9A 589/4885
US-12209145-B2 PCSK9 antagonist compounds PCSK9, PCSK7, PCSK6 SMN1; SMN2 4322/4885NPC1 121/4885RAB9A 589/4885
US-20100004441-A1 N-(5-Membered Aromatic Ring)-Amido Anti-Viral Compounds ZC3HAV1, ZC3HAV1L, HAVCR2 SMN1; SMN2 1431/4885NPC1 1259/4885RAB9A 487/4885
US-20250206781-A1 PCSK9 ANTAGONIST COMPOUNDS PCSK9, PCSK7, PCSK6 SMN1; SMN2 4322/4885NPC1 121/4885RAB9A 589/4885
US-20070265265-A1 N-(5-MEMBERED AROMATIC RING)-AMIDO ANTI-VIRAL COMPOUNDS ZC3HAV1, ZC3HAV1L, HAVCR2 SMN1; SMN2 1431/4885NPC1 1259/4885RAB9A 487/4885

“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.