SCHEMBL1477487

SCHEMBL1477487

Cc1nc2ccc(Cl)nc2c(=O)[nH]1

nearest known ligand 0.50

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 6/20 0.50
TYMS P04818 7/20 0.49
TNKS2 Q9H2K2 1/20 0.47
ADORA3 P0DMS8 3/20 0.44
KDM4E B2RXH2 2/20 0.44
LMNA P02545 1/20 0.44
HSD17B10 Q99714 1/20 0.44
ALDH1A1 P00352 2/20 0.44
NPC1 O15118 1/20 0.44
USP2 O75604 1/20 0.44
GLA P06280 1/20 0.44
GAA P10253 1/20 0.44
MAPT P10636 1/20 0.44
HPGD P15428 1/20 0.44
RAB9A P51151 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
IP6K1 Q92551 1/20 0.41

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
SCHEMBL29560266 1.00 PARP1 (0.50) PARP1TYMSTNKS2ADORA3KDM4E
SCHEMBL12912283 0.81 PARP1 (0.50) PARP1TYMSTNKS2ADORA3KDM4E
SCHEMBL826249 0.79 TYMS (0.49) TYMS
SCHEMBL3605662 0.77 KDM4E (0.49) ADORA3KDM4ELMNAHSD17B10ALDH1A1
SCHEMBL12891201 0.76 PARP1 (0.45) PARP1TYMSTNKS2ADORA3KDM4E
SCHEMBL9432425 0.76 KDM4C (0.50) PARP1TNKS2ADORA3KDM4EGLA
SCHEMBL22716291 0.74 PARP1 (0.45) PARP1TYMSTNKS2ADORA3KDM4E
SCHEMBL29439655 0.74 PARP1 (0.45) PARP1TYMSTNKS2ADORA3KDM4E
SCHEMBL30889000 0.73 ALDH1A1 (0.48) PARP1TYMSTNKS2KDM4ELMNA
SCHEMBL12909163 0.73 ALDH1A1 (0.48) PARP1TYMSTNKS2KDM4ELMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100144740-A1 SYNERGISTIC COMBINATIONS OF VR-1 ANTAGONISTS AND COX-2 INHIBITORS NOVARTIS AG (CH) 2010-06-10 US claimed
EP-2178562-A1 SYNERGISTIC COMBINATIONS OF VR-1 ANTAGONISTS AND COX-2 INHIBITORS Novartis Ag (CH) 2010-04-28 EP claimed
WO-2009010529-A1 SYNERGISTIC COMBINATIONS OF VR-1 ANTAGONISTS AND COX-2 INHIBITORS NOVARTIS AG (CH) 2009-01-22 WO claimed
US-20040138454-A1 Fused pyridine derivatives for use as vanilloid receptor antagonists for treating pain CULSHAW ANDREW JAMES (GB) 2004-07-15 US claimed
EP-1377576-A2 PYRIDINE DERIVATIVES Novartis AG (CH) 2004-01-07 EP claimed
WO-2002076946-A2 FUSED PYRIDINE DERIVATIVES FOR USE AS VANILLOID RECEPTOR ANTAGONISTS FOR TREATING PAIN. NOVARTIS AG (CH) 2002-10-03 WO claimed
CN-114269756-B 4-Oxo-3, 4-dihydropyrido [3,4-D ] pyrimidine compounds that inhibit EIF4E 效应疗法股份有限公司 2024-05-14 CN disclosed
US-20220274979-A1 2-METHYL-AZA-QUINAZOLINES BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2022-09-01 US disclosed
WO-2021003157-A1 EIF4E-INHIBITING 4-OXO-3,4-DIHYDROPYRIDO[3,4-D]PYRIMIDINE COMPOUNDS EFFECTOR THERAPEUTICS, INC. (US) 2021-01-07 WO disclosed
WO-2019201848-A1 2-METHYL-AZA-QUINAZOLINES BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2019-10-24 WO disclosed
US-8618120-B2 Synergistic combinations of VR-1 antagonists and COX-2 inhibitors NOVARTIS AG (CH) 2013-12-31 US disclosed
US-8338435-B2 Substituted pyrido(3,2-D) pyrimidines and pharmaceutical compositions for treating viral infections GILEAD SCIENCES, INC. (US) 2012-12-25 US disclosed
US-7915264-B2 Drugs for treating pain formed by arylation NOVARTIS AG (CH) 2011-03-29 US disclosed
EP-1377576-A2 PYRIDINE DERIVATIVES Novartis AG (CH) 2004-01-07 EP disclosed
US-6537999-B2 Furopyrimidines and pyrrolopyrimidines; treating cancer, and secondary infections caused by Pneumocystis carinii and Toxoplasmosis gondii in immunocompromised patients. DUQUESNE UNIVERSITY OF THE HOLY GHOST 2003-03-25 US disclosed
WO-2002076946-A2 FUSED PYRIDINE DERIVATIVES FOR USE AS VANILLOID RECEPTOR ANTAGONISTS FOR TREATING PAIN. NOVARTIS AG (CH) 2002-10-03 WO disclosed
US-6420370-B1 ANTITUMOR, ANTIBIOTIC, ANTIMALARIAL, ANTIFUNGAL OR ANTIPROTOZOAL AGENTS, OR AS SYNERGISTIC AGENTS ENZYME INHIBITORS DUQUESNE UNIVERSITY OF THE HOLY GHOST 2002-07-16 US disclosed
US-20020052384-A1 Novel pyrimidine derivatives and methods of making and using these derivatives GANGJEE ALEEM (US) 2002-05-02 US disclosed
US-6103727-A RESISTING AND TREATING PNEUNOCYSTIS CARINII AND TOXOPLASMOSIS GONDII INFECTIONS IN IMMUNOCOMPROMISED PATIENTS; AUTOMIMMUNE DISEASES; AIDS; ANTICARCINOGENIC,-TUMOR,-PROTAZOA AGENTS; MALARIA; FUNGICIDES; SYNERGISTIC WITH SULFONAMIDES DUQUESNE UNIVERSITY OF THE HOLY GHOST (US) 2000-08-15 US disclosed
US-6096750-A Furopyrimidines and methods of making and using the same derivatives DUQUESNE UNIVERSITY OF THE HOLY GHOST (US) 2000-08-01 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 (4 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-20040138454-A1 Fused pyridine derivatives for use as vanilloid receptor antagonists for treating pain TRPV1, OPRL1, OPRK1 PARP1 2409/4885TYMS 2287/4885TNKS2 2132/4885
US-20220274979-A1 2-METHYL-AZA-QUINAZOLINES AZI2, DNMT1, TPMT PARP1 195/4885TYMS 217/4885TNKS2 223/4885
US-20100144740-A1 SYNERGISTIC COMBINATIONS OF VR-1 ANTAGONISTS AND COX-2 INHIBITORS TRPV2, TRPV1, TRPV3 PARP1 2405/4885TYMS 2931/4885TNKS2 1516/4885
US-20020052384-A1 Novel pyrimidine derivatives and methods of making and using these derivatives TYMP, TYMS, DPYD PARP1 507/4885TYMS 2/4885TNKS2 276/4885

“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.