SCHEMBL518031

SCHEMBL518031

O=C(O)CCOCCOCCOCCOCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21

nearest known ligand 0.74

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FOLH1 Q04609 7/20 0.74
▸ PRSS1 P07477 2/20 0.68
▸ PRSS2 P07478 2/20 0.68
▸ PRSS3 P35030 2/20 0.68
▸ TPSAB1 Q15661 2/20 0.68
▸ F2 P00734 1/20 0.68
▸ TDP1 Q9NUW8 5/20 0.66
▸ PKM P14618 3/20 0.66
▸ MEN1 O00255 1/20 0.66
▸ ABL1 P00519 1/20 0.66
▸ LMNA P02545 1/20 0.66
▸ IDE P14735 1/20 0.66
▸ MAPK1 P28482 1/20 0.66
▸ KMT2A Q03164 1/20 0.66
▸ RIN1 Q13671 1/20 0.66
▸ L3MBTL1 Q9Y468 1/20 0.66
▸ HSP90AB1 P08238 1/20 0.58
▸ CA12 O43570 1/20 0.56
▸ CA1 P00915 1/20 0.56
▸ CA2 P00918 1/20 0.56

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
SCHEMBL30569618 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL29358108 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL31248175 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL15279176 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL17975148 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL18690250 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL31510306 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL17841934 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL13907093 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1
SCHEMBL30689887 1.00 FOLH1 (0.74) FOLH1PRSS1PRSS2PRSS3TPSAB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4713340-A2 COMPOSITIONS AND METHODS FOR PEPTIDE-BASED MODULATORS OF HUMAN PAPILLOMAVIRUS ONCOPROTEIN E6 Calico Life Sciences LLC (US) 2026-03-25 — — EP disclosed
US-20250270162-A1 KETONE INHIBITORS OF LYSINE GINGIPAIN LIGHTHOUSE PHARMACEUTICALS, INC. (US) 2025-08-28 — — US disclosed
WO-2025151487-A2 SMALL-MOLECULE INHIBITORS OF ADAR1 REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2025-07-17 — — WO disclosed
WO-2025111511-A2 REVERSIBLY REACTIVE AFFINITY SELECTION MASS SPECTROMETRY AND USES THEREOF CALICO LIFE SCIENCES LLC (US) 2025-05-30 — — WO disclosed
EP-4480541-A2 KETONE INHIBITORS OF LYSINE GINGIPAIN Lighthouse Pharmaceuticals, Inc. (US) 2024-12-25 — — EP disclosed
US-12110263-B2 Ketone inhibitors of lysine gingipain LIGHTHOUSE PHARMACEUTICALS, INC. (US) 2024-10-08 — — US disclosed
US-20240279201-A1 DUAL WNT SIGNALING PATHWAY INHIBITORS AND AMPK ACTIVATORS FOR TREATMENTS OF DISEASE UNIVERSITY OF MARYLAND, BALTIMORE 2024-08-22 — — US disclosed
EP-3512846-B1 KETONE INHIBITORS OF LYSINE GINGIPAIN LIGHTHOUSE PHARMACEUTICALS INC (US) 2024-08-14 — — EP disclosed
WO-2024124156-A1 N-HETEROCYCLIC CARBENE MONOLAYERS AS ANALYTICAL REPORTERS UNIVERSITY OF NOTRE DAME DU LAC (US) 2024-06-13 — — WO disclosed
EP-4346811-A1 DUAL WNT SIGNALING PATHWAY INHIBITORS AND AMPK ACTIVATORS FOR TREATMENTS OF DISEASE University of Maryland, Baltimore (US) 2024-04-10 — — EP disclosed
WO-2016077378-A1 SUBSTITUTED PYRROLOPYRDINES AS INHIBITORS OF BROMODOMAIN GENENTECH, INC. (US) 2016-05-19 — — WO disclosed
WO-2016077375-A1 BROMODOMAIN INHIBITORS AND USES THEREOF GENENTECH, INC. (US) 2016-05-19 — — WO disclosed
US-20140315884-A1 AMPK-ACTIVATING HETEROCYCLIC COMPOUNDS AND METHODS FOR USING THE SAME RIGEL PHARMACEUTICALS, INC. (US) 2014-10-23 — — US disclosed
US-8791136-B2 Substituted pyridine, pyridazine, pyrazine and pyrimidine compounds and methods for using the same RIGEL PHARMACEUTICALS, INC. (US) 2014-07-29 — — US disclosed
US-20130203987-A1 AMPK-ACTIVATING HETEROCYCLIC COMPOUNDS AND METHODS FOR USING THE SAME RIGEL PHARMACEUTICALS, INC. (US) 2013-08-08 — — US disclosed
EP-2598483-A1 AMPK-ACTIVATING HETEROCYCLIC COMPOUNDS AND METHODS FOR USING THE SAME Rigel Pharmaceuticals, Inc. (US) 2013-06-05 — — EP disclosed
US-8198020-B2 Contacting target cell or noncellular molecular entity with phagocytic marker and moiety that binds to a component that is present on or at surface of target cell or noncellular molecular entity, thereby increasing level or density of phagocytic marker on target cell; marker comprises phosphatidylserine POTENTIA PHARMACEUTICALS, INC. (US) 2012-06-12 — — US disclosed
US-20120028954-A1 Substituted Pyridine, Pyridazine, Pyrazine And Pyrimidine Compounds And Methods For Using The Same RIGEL PHARMACEUTICALS, INC. (US) 2012-02-02 — — US disclosed
WO-2012016217-A1 AMPK-ACTIVATING HETEROCYCLIC COMPOUNDS AND METHODS FOR USING THE SAME RIGEL PHARMACEUTICALS, INC. (US) 2012-02-02 — — WO disclosed
US-20050113297-A1 Compositions and methods for enhancing phagocytosis or phagocyte activity POTENTIA PHARMACEUTICALS, INC. 2005-05-26 — — US 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-12110263-B2 Ketone inhibitors of lysine gingipain PHYKPL, ENPEP, PREP FOLH1 280/4885PRSS1 140/4885PRSS2 389/4885
US-20120028954-A1 Substituted Pyridine, Pyridazine, Pyrazine And Pyrimidine Compounds And Methods For Using The Same AK2, PC, PRKAG2 FOLH1 3462/4885PRSS1 3397/4885PRSS2 3665/4885
US-20050113297-A1 Compositions and methods for enhancing phagocytosis or phagocyte activity CD47, ANXA11, ANXA1 FOLH1 611/4885PRSS1 382/4885PRSS2 1004/4885
US-20140315884-A1 AMPK-ACTIVATING HETEROCYCLIC COMPOUNDS AND METHODS FOR USING THE SAME PRKAG1, PRKAG2, PRKAB1 FOLH1 3645/4885PRSS1 4369/4885PRSS2 4492/4885
US-20250270162-A1 KETONE INHIBITORS OF LYSINE GINGIPAIN PHYKPL, ENPEP, PREP FOLH1 280/4885PRSS1 140/4885PRSS2 389/4885
US-20130203987-A1 AMPK-ACTIVATING HETEROCYCLIC COMPOUNDS AND METHODS FOR USING THE SAME PRKAG1, PRKAG2, PRKAB1 FOLH1 3645/4885PRSS1 4369/4885PRSS2 4492/4885
US-20240279201-A1 DUAL WNT SIGNALING PATHWAY INHIBITORS AND AMPK ACTIVATORS FOR TREATMENTS OF DISEASE PRKAB2, PRKAB1, PRKAG2 FOLH1 2503/4885PRSS1 3972/4885PRSS2 3829/4885

“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.

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