SCHEMBL1759647

SCHEMBL1759647

CC(C)(C)c1cc(C(=O)O)ccn1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.62
SMN1; SMN2 Q16637 4/20 0.58
NPC1 O15118 1/20 0.58
RAB9A P51151 1/20 0.58
HTT P42858 2/20 0.57
ALDH1A1 P00352 4/20 0.56
MEN1 O00255 1/20 0.56
MAPK1 P28482 1/20 0.56
KMT2A Q03164 1/20 0.56
KDM4C Q9H3R0 4/20 0.55
KDM4E B2RXH2 3/20 0.55
KDM6B O15054 3/20 0.55
KDM5C P41229 3/20 0.55
KDM2A Q9Y2K7 3/20 0.55
KDM3A Q9Y4C1 3/20 0.55
KDM4A O75164 2/20 0.55
ALKBH5 Q6P6C2 2/20 0.55
FTO Q9C0B1 2/20 0.55
KDM5A P29375 2/20 0.55
KDM5B Q9UGL1 2/20 0.55

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
SCHEMBL16095006 0.87 KDM4C (0.53) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL16094544 0.87 KDM4C (0.53) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL30069005 0.87 KDM4C (0.53) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL16036217 0.85 KDM4C (0.52) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL30893039 0.85 KDM4C (0.52) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL10202654 0.85 LMNA (0.58) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL31085231 0.85 LMNA (0.58) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL11347447 0.83 LMNA (0.56) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL25701470 0.82 KDM4C (0.51) LMNASMN1; SMN2NPC1RAB9AHTT
SCHEMBL25340658 0.81 KDM4C (0.47) LMNASMN1; SMN2NPC1RAB9AHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12391663-B2 Isoindolinone compounds MONTE ROSA THERAPEUTICS AG (CH) 2025-08-19 US disclosed
US-20250017914-A1 6-AZA-QUINOLINE DERIVATIVES AND RELATED USES BLACK DIAMOND THERAPEUTICS, INC. 2025-01-16 US disclosed
US-20240261274-A1 TREATMENT OF MYC-DRIVEN CANCERS WITH GSPT1 DEGRADERS MONTE ROSA THERAPEUTICS AG (CH) 2024-08-08 US disclosed
EP-4399210-A1 6-AZA-QUINOLINE DERIVATIVES AND RELATED USES Black Diamond Therapeutics, Inc. (US) 2024-07-17 EP disclosed
CN-118159537-A 6-Aza-quinoline derivatives and related uses 黑钻治疗公司 2024-06-07 CN disclosed
US-20240158372-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF AMGEN INC. 2024-05-16 US disclosed
US-20240083869-A1 ISOINDOLINONE COMPOUNDS MONTE ROSA THERAPEUTICS AG (CH) 2024-03-14 US disclosed
US-11912682-B2 Isoindolinone compounds MONTE ROSA THERAPEUTICS, INC. (US) 2024-02-27 US disclosed
CN-117343005-A Preparation method of isonicotinic acid derivative 上海泰坦科技股份有限公司 2024-01-05 CN disclosed
CN-117242060-A Isoindolinone compounds 蒙特罗萨医疗公司 2023-12-15 CN disclosed
WO-2011057973-A1 OXAZOLINE DERIVATIVES FOR TREATMENT OF CNS DISORDERS F. HOFFMANN-LA ROCHE AG (CH) 2011-05-19 WO disclosed
US-20110112080-A1 OXAZOLINE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2011-05-12 US disclosed
EP-1615919-B1 7-([1,4]DIOXAN-2-YL)-BENZOTHIAZOLE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS HOFFMANN LA ROCHE (CH) 2007-08-22 EP disclosed
CN-1774437-A 7-([1,4]dioxan-2-yl)-benzothiazole derivatives as adenosine receptor ligands HOFFMANN LA ROCHE (CH) 2006-05-17 CN disclosed
EP-1615919-A1 7-([1,4]DIOXAN-2-YL)-BENZOTHIAZOLE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS F. HOFFMANN-LA ROCHE AG (CH) 2006-01-18 EP disclosed
US-6872833-B2 Adenosine receptor ligands HOFFMANN-LA ROCHE INC. (US) 2005-03-29 US disclosed
WO-2004089949-A1 7-([1,4]DIOXAN-2-YL)-BENZOTHIAZOLE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS F. HOFFMANN-LA ROCHE AG (CH) 2004-10-21 WO disclosed
EP-0862555-B1 SUBSTITUTED ARYL OR HETEROARYLAMIDES HAVING RETINOID-LIKE BIOLOGICAL ACTIVITY ALLERGAN INC (US) 2004-10-20 EP disclosed
US-20040204584-A1 ADENOSINE RECEPTOR LIGANDS F. HOFFMANN-LA ROCHE AG (CH) 2004-10-14 US disclosed
US-6610744-B2 Administering to a mammal a retinoid campound which binds specifically or selectively to a RAR alpha retinoid receptors in preference over RAR beta and RAR Gamma retinoid receptors, for therapy and prophylaxisof disease or condition ALLERGAN, INC. 2003-08-26 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 (8 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-20240158372-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF TNNI3, TNNT2, TNNC1 LMNA 42/4885SMN1; SMN2 126/4885NPC1 4666/4885
US-12391663-B2 Isoindolinone compounds CYP4F2, AOC2, AOC3 LMNA 1164/4885SMN1; SMN2 3197/4885NPC1 285/4885
US-20240083869-A1 ISOINDOLINONE COMPOUNDS CYP4F2, AOC2, AOC3 LMNA 1164/4885SMN1; SMN2 3197/4885NPC1 285/4885
US-20040204584-A1 ADENOSINE RECEPTOR LIGANDS ADORA1, ADORA2A, ADORA3 LMNA 3437/4885SMN1; SMN2 3519/4885NPC1 1169/4885
US-20250017914-A1 6-AZA-QUINOLINE DERIVATIVES AND RELATED USES TOP2A, TOP2B, UGT2B7 LMNA 2740/4885SMN1; SMN2 1897/4885NPC1 1080/4885
US-11912682-B2 Isoindolinone compounds CYP4F2, AOC2, AOC3 LMNA 1164/4885SMN1; SMN2 3197/4885NPC1 285/4885
US-20110112080-A1 OXAZOLINE DERIVATIVES TAAR1, HCRTR1, NPY1R LMNA 3754/4885SMN1; SMN2 2163/4885NPC1 785/4885
US-20240261274-A1 TREATMENT OF MYC-DRIVEN CANCERS WITH GSPT1 DEGRADERS MYC, MYCBP, GSPT1 LMNA 3911/4885SMN1; SMN2 3190/4885NPC1 3437/4885

“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.