SCHEMBL6697405

SCHEMBL6697405

Cc1nc2ncc(C(=O)NCc3ccc(Cl)cc3)c(O)c2cc1Br

nearest known ligand 0.52

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
EGLN1 Q9GZT9 1/20 0.47
CYP1A1 P04798 1/20 0.47
HPGD P15428 1/20 0.47
LMNA P02545 4/20 0.46
NR3C1 P04150 2/20 0.46
POLA1 P09884 2/20 0.46
SMN1; SMN2 Q16637 3/20 0.46
KMT2A Q03164 2/20 0.46
MEN1 O00255 1/20 0.46
ALDH1A1 P00352 1/20 0.46
TSHR P16473 1/20 0.46
ADORA2A P29274 1/20 0.44
ADORA1 P30542 1/20 0.44
THRB P10828 1/20 0.44
TP53 P04637 1/20 0.43
GALR3 O60755 1/20 0.42
NR2F2 P24468 1/20 0.42
RAB9A P51151 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
SCHEMBL6696378 0.87 EGLN1 (0.47) EGLN1CYP1A1HPGDLMNANR3C1
SCHEMBL6691160 0.85 LMNA (0.47) EGLN1CYP1A1HPGDLMNANR3C1
SCHEMBL6695156 0.84 ADORA2A (0.57) EGLN1CYP1A1HPGDLMNANR3C1
SCHEMBL6699580 0.82 EGLN1 (0.43) EGLN1CYP1A1HPGDLMNANR3C1
SCHEMBL6699267 0.79 MAPK1 (0.42) EGLN1CYP1A1HPGDLMNANR3C1
SCHEMBL6692811 0.79 KCNH2 (0.51) POLA1KMT2AMEN1ALDH1A1TSHR
SCHEMBL6202038 0.78 EGLN1 (0.54) EGLN1HPGDLMNANR3C1POLA1
SCHEMBL15336604 0.77 POLA1 (0.47) EGLN1CYP1A1HPGDLMNANR3C1
SCHEMBL6200288 0.77 AKR1B1 (0.48) EGLN1HPGDLMNANR3C1POLA1
SCHEMBL6198601 0.77 EGLN1 (0.50) EGLN1CYP1A1HPGDLMNANR3C1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040067947-A1 Method of preventing or treating atherosclerosis or restenosis WATHEN MICHAEL W 2004-04-08 US claimed
EP-1265896-A1 4-HYDROXY-1,8-NAPHTHYRIDINE-3-CARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2002-12-18 EP claimed
US-6413958-B2 FOR TREATMENT/PREVENTION OF INFECTION OF HERPES SIMPLEX VIRUS, VARICELLA ZOSTER VIRUS, HUMAN CYTOMEGALOVIRUS, OR EPSTEIN-BARR VIRUS; ENZYME INHIBITORS PHARMACIA & UPJOHN COMPANY 2002-07-02 US claimed
US-20020007066-A1 4-hydroxy-1,8-naphthyridine-3-carboxamides as antiviral agents PHARMACIA & UPJOHN COMPANY 2002-01-17 US claimed
WO-2001070742-A1 4-HYDROXY-1,8-NAPHTHYRIDINE-3-CARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2001-09-27 WO claimed
US-20040067947-A1 Method of preventing or treating atherosclerosis or restenosis WATHEN MICHAEL W 2004-04-08 US disclosed
US-6693114-B2 N-(4-CHLOROBENZYL)-6-(3-HYDROXY-1-PROPYNYL)-1-7-DIMETHYL-4-OXO-1,4 -DIHYDRO(1,8) NAPHTHYRIDINE-3-CARBOXAMIDE FOR EXAMPLE; INHIBITING VIRAL DNA POLYMERASE; TREATING HERPES VIRUS INFECTIONS PHARMACIA & UPJOHN COMPANY 2004-02-17 US disclosed
EP-1265896-A1 4-HYDROXY-1,8-NAPHTHYRIDINE-3-CARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2002-12-18 EP disclosed
EP-1265895-A1 4-OXO-1,4-DIHYDRO 1,8]NAPHTHYRIDINE-3-CARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2002-12-18 EP disclosed
US-20020177604-A1 4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxamides as antiviral agents VAILLANCOURT VALERIE A (US) 2002-11-28 US disclosed
US-6451811-B2 HERPES VIRUS PHARMACIA & UPJOHN COMPANY 2002-09-17 US disclosed
US-6413958-B2 FOR TREATMENT/PREVENTION OF INFECTION OF HERPES SIMPLEX VIRUS, VARICELLA ZOSTER VIRUS, HUMAN CYTOMEGALOVIRUS, OR EPSTEIN-BARR VIRUS; ENZYME INHIBITORS PHARMACIA & UPJOHN COMPANY 2002-07-02 US disclosed
US-20020019413-A1 4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxamides as antiviral agents PHARMACIA & UPJOHN COMPANY 2002-02-14 US disclosed
US-20020007066-A1 4-hydroxy-1,8-naphthyridine-3-carboxamides as antiviral agents PHARMACIA & UPJOHN COMPANY 2002-01-17 US disclosed
WO-2001074816-A1 4-OXO-1,4-DIHYDRO[1,8]NAPHTHYRIDINE-3-CARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2001-10-11 WO disclosed
WO-2001070742-A1 4-HYDROXY-1,8-NAPHTHYRIDINE-3-CARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2001-09-27 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 (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-20020019413-A1 4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxamides as antiviral agents IRF3, ZC3HAV1, EIF2AK2 EGLN1 1009/4885CYP1A1 1780/4885HPGD 2127/4885
US-20020177604-A1 4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxamides as antiviral agents IRF3, ZC3HAV1, EIF2AK2 EGLN1 1009/4885CYP1A1 1780/4885HPGD 2127/4885
US-20020007066-A1 4-hydroxy-1,8-naphthyridine-3-carboxamides as antiviral agents CNR1, HAVCR2, NR1H4 EGLN1 569/4885CYP1A1 936/4885HPGD 1309/4885
US-20040067947-A1 Method of preventing or treating atherosclerosis or restenosis LDLR, MSR1, NR1H2 EGLN1 1633/4885CYP1A1 2804/4885HPGD 552/4885

“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.