SCHEMBL429230

SCHEMBL429230

CC(C)(C)OC(=O)Nc1ccsc1C(=O)O

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN2 P17706 1/20 0.57
PTPN1 P18031 1/20 0.57
ABCC1 P33527 1/20 0.54
MEN1 O00255 5/20 0.52
KMT2A Q03164 5/20 0.52
NPC1 O15118 5/20 0.52
RAB9A P51151 4/20 0.52
METAP1 P53582 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.44
LMNA P02545 2/20 0.44
RXFP1 Q9HBX9 2/20 0.43
PRNP P04156 1/20 0.43
PPARG P37231 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43
NCOR2 Q9Y618 1/20 0.43
HPGD P15428 2/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
KDM4E B2RXH2 1/20 0.42
ALDH1A1 P00352 1/20 0.42
GLA P06280 1/20 0.42

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
SCHEMBL7457637 0.88 NPSR1 (0.50) PTPN2PTPN1ABCC1NPC1METAP1
SCHEMBL2106155 0.86 NPC1 (0.66) MEN1KMT2ANPC1L3MBTL1LMNA
SCHEMBL28881226 0.85 METAP1 (0.48) PTPN2PTPN1MEN1KMT2ANPC1
SCHEMBL7462727 0.85 NPC1 (0.46) PTPN2PTPN1ABCC1KMT2ANPC1
SCHEMBL5620033 0.84 METAP1 (0.47) ABCC1MEN1KMT2ANPC1RAB9A
SCHEMBL1704198 0.83 LMNA (0.51) MEN1KMT2ANPC1RAB9AMETAP1
SCHEMBL9291119 0.82 METAP1 (0.50) MEN1KMT2ANPC1METAP1LMNA
SCHEMBL15640149 0.81 MAPK8 (0.58) MEN1KMT2ANPC1RAB9AL3MBTL1
SCHEMBL14510093 0.81 METAP1 (0.49) NPC1METAP1LMNARXFP1HPGD
SCHEMBL6242277 0.80 METAP1 (0.46) NPC1METAP1L3MBTL1LMNARXFP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240158357-A1 NOVEL QUINAZOLINONES THAT INHIBIT THE FORMATION OF TAU OLIGOMERS AND THEIR METHOD OF USE OLIGOMERIX, INC. (US) 2024-05-16 US disclosed
EP-4252856-A2 NOVEL QUINAZOLINONES THAT INHIBIT THE FORMATION OF TAU OLIGOMERS AND THEIR METHOD OF USE Oligomerix, Inc. (US) 2023-10-04 EP disclosed
EP-3558950-B1 NOVEL QUINAZOLINONES THAT INHIBIT THE FORMATION OF TAU OLIGOMERS AND THEIR METHOD OF USE OLIGOMERIX INC (US) 2023-05-10 EP disclosed
CN-114213400-B Thiophene-containing pyrimidine compound and preparation method and application thereof 贵州大学 2022-11-08 CN disclosed
US-11472776-B2 Quinazolinones that inhibit the formation of tau oligomers and their method of use OLIGOMERIX, INC. (US) 2022-10-18 US disclosed
CN-114213400-A Thiophene-containing pyrimidine compound and preparation method and application thereof 贵州大学 2022-03-22 CN disclosed
US-20190345115-A1 NOVEL QUINAZOLINONES THAT INHIBIT THE FORMATION OF TAU OLIGOMERS AND THEIR METHOD OF USE OLIGOMERIX, INC. 2019-11-14 US disclosed
CN-104822653-B N-prop-2-ynylcarboxamide derivatives and their use as TRPA1 antagonists 奥赖恩公司 2017-03-08 CN disclosed
EP-2903965-B1 N-PROP-2-YNYL CARBOXAMIDE DERIVATIVES AND THEIR USE AS TRPA1 ANTAGONISTS ORION CORP (FI) 2017-03-01 EP disclosed
US-9533952-B2 N-prop-2-ynyl carboxamide derivatives and their use as TRPA1 antagonists ORION CORPORATION (FI) 2017-01-03 US disclosed
US-20030225106-A1 Substituted alkylamine derivatives and methods of use AMGEN INC. 2003-12-04 US disclosed
EP-1358184-A1 SUBSTITUTED ALKYLAMINE DERIVATIVES AND METHODS OF USE Amgen Inc. (US) 2003-11-05 EP disclosed
US-20030125339-A1 Substituted alkylamine derivatives and methods of use AMGEN INC. 2003-07-03 US disclosed
WO-2002066470-A1 SUBSTITUTED ALKYLAMINE DERIVATIVES AND METHODS OF USE AMGEN INC. (US) 2002-08-29 WO disclosed
US-5869427-A Substituted thiophene derivative and plant disease control agent comprising the same as active ingredient MITSUI CHEMICALS, INC. (JP) 1999-02-09 US disclosed
EP-0841336-A1 Substituted thiopene derivative and plant disease control agent comprising the same as active ingredient MITSUI TOATSU CHEMICALS, Inc. (JP) 1998-05-13 EP disclosed
EP-0609371-B1 THIENOPYRAZINE-2,3-DIONES USEFUL FOR TREATING CNS DISORDERS, AND THEIR PREPARATION. NOVO NORDISK AS (DK) 1996-04-24 EP disclosed
EP-0609371-A1 THIENOPYRAZINE-2,3-DIONES AND THEIR PREPARATION AND USE. NOVO NORDISK AS (DK) 1994-08-10 EP disclosed
US-5284847-A Neurological and psychological disorders; antagonist at the glycine binding site on the N-methyl-D-aspartate receptor complex NOVO NORDISK A/S (DK) 1994-02-08 US disclosed
WO-1993008197-A1 THIENOPYRAZINE-2,3-DIONES AND THEIR PREPARATION AND USE NOVO NORDISK A/S (DK) 1993-04-29 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 (5 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-20030225106-A1 Substituted alkylamine derivatives and methods of use NAT1, PIGO, AADAC PTPN2 3095/4885PTPN1 2756/4885ABCC1 806/4885
US-20030125339-A1 Substituted alkylamine derivatives and methods of use AADAC, NAT1, PIGO PTPN2 3141/4885PTPN1 2862/4885ABCC1 609/4885
US-20190345115-A1 NOVEL QUINAZOLINONES THAT INHIBIT THE FORMATION OF TAU OLIGOMERS AND THEIR METHOD OF USE MAPT, PSEN1, APP PTPN2 3278/4885PTPN1 3370/4885ABCC1 1527/4885
US-11472776-B2 Quinazolinones that inhibit the formation of tau oligomers and their method of use MAPT, PSEN1, APP PTPN2 3089/4885PTPN1 3100/4885ABCC1 1438/4885
US-20240158357-A1 NOVEL QUINAZOLINONES THAT INHIBIT THE FORMATION OF TAU OLIGOMERS AND THEIR METHOD OF USE MAPT, PSEN1, APP PTPN2 3278/4885PTPN1 3370/4885ABCC1 1527/4885

“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.