SCHEMBL524586

SCHEMBL524586

COc1ccc(CCNCC(=O)O)cc1

nearest known ligand 0.64

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 6/20 0.64
MEN1 O00255 5/20 0.64
ATM Q13315 2/20 0.64
SMN1; SMN2 Q16637 2/20 0.61
ALDH1A1 P00352 3/20 0.59
KDM4E B2RXH2 1/20 0.57
GAA P10253 1/20 0.57
TDP1 Q9NUW8 1/20 0.57
FFAR1 O14842 2/20 0.56
TAAR1 Q96RJ0 1/20 0.56
F2RL1 P55085 1/20 0.56
GLA P06280 1/20 0.55
FPR2 P25090 1/20 0.55
LMNA P02545 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54

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
SCHEMBL31369624 0.90 S1PR1 (0.55) KMT2AMEN1ATMSMN1; SMN2FFAR1
SCHEMBL3196104 0.89 MEN1 (0.62) KMT2AMEN1ATMSMN1; SMN2ALDH1A1
SCHEMBL9544789 0.87 SMN1; SMN2 (0.61) KMT2AMEN1ATMSMN1; SMN2ALDH1A1
SCHEMBL13113227 0.87 SMN1; SMN2 (0.66) KMT2AMEN1ATMSMN1; SMN2ALDH1A1
SCHEMBL4459745 0.85 SMN1; SMN2 (0.59) KMT2AMEN1ATMSMN1; SMN2ALDH1A1
SCHEMBL6066919 0.84 MEN1 (0.50) KMT2AMEN1ATMSMN1; SMN2ALDH1A1
Ammonia Solution, Strong SCHEMBL6066933 0.84 KMT2A (0.50) KMT2AMEN1ATMSMN1; SMN2ALDH1A1
SCHEMBL9487686 0.83 MEN1 (0.60) KMT2AMEN1ATMSMN1; SMN2ALDH1A1
SCHEMBL1807496 0.83 MEN1 (0.61) KMT2AMEN1ATMALDH1A1KDM4E
SCHEMBL13101471 0.83 KMT2A (0.56) KMT2AMEN1ATMSMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7026282-B1 Peptide antagonists of the human urokinase receptor and method for selecting them Cancerforskningsfonden AF 1989 (Fonden Til Fremme AF Exsperimentel Cancerforskning) (DK) 2006-04-11 US claimed
WO-2000001802-A2 PEPTIDE ANTAGONISTS OF THE HUMAN UROKINASE RECEPTOR AND METHOD FOR SELECTING THEM CANCERFORSKNINGSFONDEN AF 1989 (FONDEN TIL FREMME AF EKSPERIMENTEL CANCERFORSKNING) (DK) 2000-01-13 WO claimed
US-12281180-B2 Peptoid-peptide macrocycles, pharmaceutical compositions and methods of using the same NEW YORK UNIVERSITY (US) 2025-04-22 US disclosed
WO-2024040245-A1 PEPTIDE DERIVATIVES AND RELATED USES AS OREXIN AGONISTS CENTESSA PHARMACEUTICALS (OREXIA) LIMITED (GB) 2024-02-22 WO disclosed
WO-2024040237-A1 PEPTIDE DERIVATIVES AND RELATED USES AS OREXIN AGONISTS CENTESSA PHARMACEUTICALS (OREXIA) LIMITED (GB) 2024-02-22 WO disclosed
WO-2024015797-A1 PEPTIDE DERIVATIVES AND RELATED USES AS OREXIN AGONISTS CENTESSA PHARMACEUTICALS (OREXIA) LIMITED (GB) 2024-01-18 WO disclosed
WO-2023017180-A1 PEPTIDE DERIVATIVES AND RELATED USES AS OREXIN AGONISTS OREXIA THERAPEUTICS LIMITED (GB) 2023-02-16 WO disclosed
US-20130109581-A1 POSITIVELY CHARGED SPECIES AS BINDING REAGENTS IN THE SEPARATION OF PROTEIN AGGREGATES FROM MONOMERS NOVARTIS AG (CH) 2013-05-02 US disclosed
EP-1931695-B1 Prion-specific peptoid reagents NOVARTIS AG (CH) 2013-04-10 EP disclosed
EP-2496947-A1 POSITIVELY CHARGED SPECIES AS BINDING REAGENTS IN THE SEPARATION OF PROTEIN AGGREGATES FROM MONOMERS Novartis AG (CH) 2012-09-12 EP disclosed
US-20120027677-A1 Prion-specific peptoid reagents NOVARTIS AG 2012-02-02 US disclosed
WO-2011057029-A1 POSITIVELY CHARGED SPECIES AS BINDING REAGENTS IN THE SEPARATION OF PROTEIN AGGREGATES FROM MONOMERS NOVARTIS AG (CH) 2011-05-12 WO disclosed
EP-2282753-A1 ASSAY FOR PATHOGENIC CONFORMERS Novartis AG (CH) 2011-02-16 EP disclosed
US-7834144-B2 Prion-specific peptoid reagents NOVARTIS AG (CH) 2010-11-16 US disclosed
WO-2009134942-A1 ASSAY FOR PATHOGENIC CONFORMERS NOVARTIS AG. (CH) 2009-11-05 WO disclosed
EP-1931695-A1 PRION-SPECIFIC PEPTOID REAGENTS Novartis AG (CH) 2008-06-18 EP disclosed
US-20070087972-A1 Prion-specific peptoid reagents NOVARTIS AG (CH) 2007-04-19 US disclosed
WO-2007030804-A1 PRION-SPECIFIC PEPTOID REAGENTS NOVARTIS AG (CH) 2007-03-15 WO disclosed
US-7026282-B1 Peptide antagonists of the human urokinase receptor and method for selecting them Cancerforskningsfonden AF 1989 (Fonden Til Fremme AF Exsperimentel Cancerforskning) (DK) 2006-04-11 US disclosed
WO-2000001802-A2 PEPTIDE ANTAGONISTS OF THE HUMAN UROKINASE RECEPTOR AND METHOD FOR SELECTING THEM CANCERFORSKNINGSFONDEN AF 1989 (FONDEN TIL FREMME AF EKSPERIMENTEL CANCERFORSKNING) (DK) 2000-01-13 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 (3 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-20070087972-A1 Prion-specific peptoid reagents PRNP, PARL, PCNP KMT2A 4687/4885MEN1 2738/4885ATM 4712/4885
US-20120027677-A1 Prion-specific peptoid reagents PRNP, PARL, PCNP KMT2A 4687/4885MEN1 2738/4885ATM 4712/4885
US-12281180-B2 Peptoid-peptide macrocycles, pharmaceutical compositions and methods of using the same WNT1, WNT3, WNT3A KMT2A 4855/4885MEN1 1000/4885ATM 2394/4885

“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.