SCHEMBL3103486

SCHEMBL3103486

NCC(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc2ccccc2c1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 2/20 0.58
MAOA P21397 1/20 0.58
HDAC8 Q9BY41 5/20 0.53
HDAC3 O15379 2/20 0.53
HDAC4 P56524 2/20 0.53
HDAC1 Q13547 2/20 0.53
HDAC7 Q8WUI4 2/20 0.53
HDAC2 Q92769 2/20 0.53
HDAC10 Q969S8 2/20 0.53
HDAC11 Q96DB2 2/20 0.53
HDAC6 Q9UBN7 2/20 0.53
HDAC9 Q9UKV0 2/20 0.53
HDAC5 Q9UQL6 2/20 0.53
TRHDE Q9UKU6 1/20 0.52
SMN1; SMN2 Q16637 2/20 0.51
MEN1 O00255 2/20 0.50
CYP1A2 P05177 2/20 0.50
KMT2A Q03164 2/20 0.50
FCER2 P06734 2/20 0.50
KDM4E B2RXH2 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
SCHEMBL29802269 1.00 KDM1A (0.58) KDM1AMAOAHDAC8HDAC3HDAC4
SCHEMBL17329292 1.00 KDM1A (0.58) KDM1AMAOAHDAC8HDAC3HDAC4
SCHEMBL7860801 0.83 LTA4H (0.51) KDM1AMAOAHDAC8HDAC3HDAC4
SCHEMBL7859203 0.82 LTA4H (0.55) KDM1AMAOATRHDESMN1; SMN2FCER2
SCHEMBL12856056 0.82 MEN1 (0.54) KDM1AMAOATRHDEMEN1KMT2A
SCHEMBL13865248 0.82 MEN1 (0.54) KDM1AMAOATRHDEMEN1KMT2A
SCHEMBL9489894 0.81 MEN1 (0.49) HDAC4HDAC1SMN1; SMN2MEN1CYP1A2
SCHEMBL2306692 0.81 PIN1 (0.50) FCER2
SCHEMBL1614525 0.80 BACE1 (0.54) HDAC8SMN1; SMN2MEN1CYP1A2KMT2A
SCHEMBL5145729 0.80 BACE1 (0.54) HDAC8SMN1; SMN2MEN1CYP1A2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240409935-A1 Atg8ylation coordinates stress granule formation and mTOR inactivation in response to lysosomal damage UNM RAINFOREST INNOVATIONS (US) 2024-12-12 US claimed
US-20210069295-A1 GALECTINS CONTROL MTOR IN RESPONSE TO ENDOMEMBRANE DAMAGE AND PROVIDE A MECHANISM AND TARGET FOR THE TREATMENT OF AUTOPHAGY-RELATED DISEASES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2021-03-11 US claimed
EP-4731259-A1 A NANOFORMULATION FOR THERAPEUTIC USE Council of Scientific and Industrial Research (IN) 2026-04-29 EP disclosed
US-12216121-B2 Methods and compositions for spacial and temporal measurement of catalytic activity THE UNIVERSITY OF CHICAGO (US) 2025-02-04 US disclosed
US-20250027956-A1 Improved Gamma-Secretase Inhibitor Screening Assays KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2025-01-23 US disclosed
US-20240409935-A1 Atg8ylation coordinates stress granule formation and mTOR inactivation in response to lysosomal damage UNM RAINFOREST INNOVATIONS (US) 2024-12-12 US disclosed
US-12133720-B2 Methods and compositions for restoring homeostatic capacity of a subject Palo Alto Investors LP (US) 2024-11-05 US disclosed
EP-4433828-A1 IMPROVED GAMMA-SECRETASE INHIBITOR SCREENING ASSAYS VIB VZW (BE) 2024-09-25 EP disclosed
US-11819498-B2 Methods and compositions for treating autophagy related disease states and conditions utilizing AMPK activation UNM RAINFOREST INNOVATIONS (US) 2023-11-21 US disclosed
WO-2023089062-A1 IMPROVED GAMMA-SECRETASE INHIBITOR SCREENING ASSAYS VIB VZW (BE) 2023-05-25 WO disclosed
US-20220315548-A1 SMALL MOLECULE AGONISTS OF MUCOLIPIN 1 AND USES THEREOF NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES 2022-10-06 US disclosed
US-20020022003-A1 METHOD AND COMPOSITION FOR THE TREATMENT OF CANCER BY THE ENZYMANTIC CONVERSION OF SOLUBLE RADIOACTIVE TOXIC PRECIPITATES IN THE CANCER ROSE SAMUEL (US) 2002-02-21 US disclosed
US-5668112-A Hydrophobic peptide esters and amides BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYS. (US) 1997-09-16 US disclosed
EP-0604416-A1 IDENTIFYING MEMBRANOLYTIC COMPOUNDS AND PRECURSORS THEREOF THE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1994-07-06 EP disclosed
US-5304474-A Deactivation of killer cells or cytotoxic lymphocytes BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1994-04-19 US disclosed
WO-1993005394-A1 IDENTIFYING MEMBRANOLYTIC COMPOUNDS AND PRECURSORS THEREOF BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1993-03-18 WO disclosed
EP-0255341-B1 REAGENT FOR TESTING PERIODONTAL DISEASES SUNSTAR KABUSHIKI KAISHA (JP) 1993-02-03 EP disclosed
US-5137811-A Method for diagnosing periodontal diseases with a substrate specific for aminopeptidase activity of periodontopathic bacteria SUNSTAR KABUSHIKI KAISHA (JP) 1992-08-11 US disclosed
US-5068223-A Dipeptides and derivatives used to deplete cytotoxic lymphocytes BOARD OF REGENTS, UNIVERSITY OF TEXAS SYSTEM 1991-11-26 US disclosed
EP-0255341-A2 Reagent for testing periodontal diseases SUNSTAR KABUSHIKI KAISHA (JP) 1988-02-03 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 (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-20220315548-A1 SMALL MOLECULE AGONISTS OF MUCOLIPIN 1 AND USES THEREOF MCOLN1, MCOLN2, MCOLN3 KDM1A 2664/4885MAOA 3355/4885HDAC8 1020/4885
US-12216121-B2 Methods and compositions for spacial and temporal measurement of catalytic activity RNGTT, SCLY, RNASEL KDM1A 3541/4885MAOA 1579/4885HDAC8 2700/4885
US-20240409935-A1 Atg8ylation coordinates stress granule formation and mTOR inactivation in response to lysosomal damage LAMTOR3, MLST8, ATG7 KDM1A 3286/4885MAOA 4752/4885HDAC8 243/4885

“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.