SCHEMBL1976948

SCHEMBL1976948

COCC(=O)Nc1ccc(O)cc1

nearest known ligand 0.71

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
HPGD P15428 6/20 0.71
ALDH1A1 P00352 4/20 0.71
MAPT P10636 2/20 0.67
SMN1; SMN2 Q16637 2/20 0.67
ALOX12 P18054 1/20 0.67
MAPK1 P28482 1/20 0.67
HTT P42858 1/20 0.67
RAB9A P51151 2/20 0.61
NPC1 O15118 1/20 0.60
KDM4C Q9H3R0 1/20 0.59
CYP2C19 P33261 1/20 0.57
MTNR1A P48039 1/20 0.55
MTNR1B P49286 1/20 0.55
CYP1A1 P04798 1/20 0.55
KMT2A Q03164 2/20 0.54
MEN1 O00255 1/20 0.54
KDM4E B2RXH2 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
NAMPT P43490 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
SCHEMBL14962804 0.92 HPGD (0.81) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL764569 0.85 HPGD (0.71) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL22854085 0.85 HPGD (0.71) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL14075478 0.84 ALDH1A1 (0.57) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL2091479 0.83 HPGD (0.70) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL2098410 0.83 MTNR1A (0.70) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL16299514 0.83 HPGD (0.69) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL853933 0.83 HPGD (0.70) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL971460 0.83 HPGD (1.00) HPGDALDH1A1MAPTSMN1; SMN2ALOX12
SCHEMBL588524 0.82 HPGD (0.86) HPGDALDH1A1MAPTSMN1; SMN2ALOX12

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4381284-B1 LIGAND-TARGET INTERACTION ANALYSIS BY PHOTOCHEMICALLY INDUCED DYNAMIC NUCLEAR POLARIZATION (PHOTO-CIDNP) ENHANCED NMR SPECTROSCOPY ETH ZUERICH (CH) 2025-07-09 EP disclosed
US-20240345008-A1 LIGAND-TARGET INTERACTION ANALYSIS BY PHOTOCHEMICALLY INDUCED DYNAMIC NUCLEAR POLARIZATION (PHOTO-CIDNP) ENHANCED NMR SPECTROSCOPY ETH ZURICH (CH) 2024-10-17 US disclosed
EP-2332910-B1 New derivatives of azabicyclo[3.2.0]hept-3-yl, method for preparing same and pharmaceutical compositions containing them SERVIER LAB (FR) 2013-01-30 EP disclosed
US-20120283245-A1 AZABICYCLO[3.1.0]HEX-2-YL COMPOUNDS, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM LES LABORATOIRES SERVIER (FR) 2012-11-08 US disclosed
EP-2509947-A1 AZABICYCLO[3.1.0]HEX-2-YL DERIVATIVES, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME Les Laboratoires Servier (FR) 2012-10-17 EP disclosed
US-8008337-B2 Azabicyclo[3.2.0] hept-3-yl compounds, a process for their preparation and pharmaceutical compositions containing them LES LABORATOIRES SERVIER (FR) 2011-08-30 US disclosed
WO-2011070251-A1 NOVEL HEXAHYDROCYCLOPENTA[B]PYRROL DERIVATIVES, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME LES LABORATOIRES SERVIER (FR) 2011-06-16 WO disclosed
WO-2011070252-A1 AZABICYCLO[3.2.0]HEPT-6-YL DERIVATIVES AS ANTAGONISTS OF HISTAMINE H3 RECEPTOR LES LABORATOIRES SERVIER (FR) 2011-06-16 WO disclosed
WO-2011070253-A1 AZABICYCLO[3.1.0]HEX-2-YL DERIVATIVES, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME LES LABORATOIRES SERVIER (FR) 2011-06-16 WO disclosed
WO-2011070250-A1 NOVEL AZABICYCLO[3.2.0]HEPT-3-YL DERIVATIVES, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME LES LABORATOIRES SERVIER (FR) 2011-06-16 WO disclosed
EP-2332910-A1 New derivatives of azabicyclo[3.2.0]hept-3-yl, method for preparing same and pharmaceutical compositions containing them Les Laboratoires Servier (FR) 2011-06-15 EP disclosed
US-20110136886-A1 Azabicyclo[3.2.0] hept-3-yl compounds, a process for their preparation and pharmaceutical compositions containing them LES LABORATOIRES SERVIER (FR) 2011-06-09 US disclosed
US-7906547-B2 Azabicylic compounds, a process for their preparation and pharmaceutical compositions containing them LES LABORATOIRES SERVIER (FR) 2011-03-15 US disclosed
US-20090312389-A1 Azabicylic compounds, a process for their preparation and pharmaceutical compositions containing them LES LABORATOIRES SERVIER (FR) 2009-12-17 US disclosed
WO-2009150331-A1 NOVEL AZABICYCLIC DERIVATIVES, PREPARATION METHOD FOR SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME LES LABORATOIRES SERVIER (FR) 2009-12-17 WO disclosed
EP-2133333-A1 New azabicyclic derivatives, method of preparing same and pharmaceutical compositions containing them Les Laboratoires Servier (FR) 2009-12-16 EP disclosed
US-7419934-B2 Reversible thermosensitive coloring material and reversible thermosensitive recording material using the reversible thermosensitive coloring material RICOH COMPANY LIMITED (JP) 2008-09-02 US disclosed
US-20070259782-A1 REVERSIBLE THERMOSENSITIVE COLORING MATERIAL AND REVERSIBLE THERMOSENSITIVE RECORDING MATERIAL USING THE REVERSIBLE THERMOSENSITIVE COLORING MATERIAL RICOH COMPANY, LIMITED (JP) 2007-11-08 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 (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-20120283245-A1 AZABICYCLO[3.1.0]HEX-2-YL COMPOUNDS, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AGER, AZI2, HTT HPGD 1630/4885ALDH1A1 310/4885MAPT 52/4885
US-20110136886-A1 Azabicyclo[3.2.0] hept-3-yl compounds, a process for their preparation and pharmaceutical compositions containing them HRH2, HRH4, HRH3 HPGD 666/4885ALDH1A1 427/4885MAPT 2026/4885
US-20090312389-A1 Azabicylic compounds, a process for their preparation and pharmaceutical compositions containing them CHAT, MAOB, ALKBH2 HPGD 3539/4885ALDH1A1 218/4885MAPT 294/4885

“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.