SCHEMBL919984

SCHEMBL919984

O=C(Cl)c1cc(F)c(Cl)nc1Cl

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KEAP1 Q14145 1/20 0.71
NFE2L2 Q16236 1/20 0.71
ALDH1A1 P00352 1/20 0.42
ALOX15 P16050 1/20 0.42
CASP1 P29466 2/20 0.34
CTNNB1 P35222 1/20 0.33
TCF7L2 Q9NQB0 1/20 0.33
POLB P06746 1/20 0.33
APEX1 P27695 1/20 0.33
HPGD P15428 2/20 0.33
PLAU P00749 1/20 0.32
ELANE P08246 1/20 0.32
MAPT P10636 1/20 0.32
TSHR P16473 1/20 0.32
MAOB P27338 1/20 0.32
ACKR3 P25106 1/20 0.31
MMP2 P08253 1/20 0.31
MMP9 P14780 1/20 0.31
KMO O15229 3/20 0.31
NPC1 O15118 1/20 0.31

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
SCHEMBL31048928 1.00 KEAP1 (0.71) KEAP1NFE2L2ALDH1A1ALOX15CASP1
SCHEMBL29744459 0.83 KEAP1 (1.00) KEAP1NFE2L2ALDH1A1CASP1CTNNB1
SCHEMBL113812 0.83 KEAP1 (1.00) KEAP1NFE2L2ALDH1A1CASP1CTNNB1
Hydrochloric Acid SCHEMBL919985 0.82 KEAP1 (0.96) KEAP1NFE2L2ALDH1A1CASP1CTNNB1
SCHEMBL30474526 0.82 KEAP1 (0.69) KEAP1NFE2L2CASP1POLB
SCHEMBL166218 0.82 KEAP1 (0.69) KEAP1NFE2L2CASP1POLB
SCHEMBL10518552 0.82 KEAP1 (0.69) KEAP1NFE2L2ALDH1A1CASP1CTNNB1
SCHEMBL5871710 0.80 KEAP1 (0.61) KEAP1NFE2L2CASP1CTNNB1TCF7L2
SCHEMBL20788868 0.80 KEAP1 (0.61) KEAP1NFE2L2ALDH1A1CASP1CTNNB1
SCHEMBL31048876 0.79 KEAP1 (0.65) KEAP1NFE2L2CTNNB1TCF7L2POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117732272-A Mixed matrix membrane with high stability, preparation method and application 江苏大学 2024-03-22 CN claimed
CN-115703648-A Modified zinc oxide, preparation method thereof and light-emitting diode TCL科技集团股份有限公司 2023-02-17 CN claimed
EP-0187376-A2 6,7-Disubstituted 1-cyclopropyl-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids BAYER AG (DE) 1986-07-16 EP claimed
US-20260132127-A1 NOVEL SPIRO COMPOUND MITSUBISHI TANABE PHARMA CORPORATION (JP) 2026-05-14 US disclosed
EP-4716531-A2 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS Board of Regents, The University of Texas System (US) 2026-04-01 EP disclosed
US-20260070925-A1 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS UNIV TEXAS (US) 2026-03-12 US disclosed
US-20260022118-A1 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS UNIV TEXAS (US) 2026-01-22 US disclosed
EP-4626427-A1 COMBINATIONS COMPRISING A MENIN-MLL INHIBITOR AND A BCL-2 INHIBITOR Janssen Pharmaceutica NV (BE) 2025-10-08 EP disclosed
EP-4626426-A1 COMBINATIONS COMPRISING A MENIN-MLL INHIBITOR AND AT LEAST ONE OTHER THERAPEUTIC AGENT JANSSEN Pharmaceutica NV (BE) 2025-10-08 EP disclosed
US-20250302840-A1 COMBINATION THERAPIES JANSSEN-CILAG (FR) 2025-10-02 US disclosed
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORP (US) 2025-06-12 US disclosed
US-4840954-A BACTERICIDE BAYER AKTIENGESELLSCHAFT (DE) 1989-06-20 US disclosed
EP-0302372-A1 Naphthyridine antianaerobic compounds ABBOTT LABORATORIES (US) 1989-02-08 EP disclosed
US-4738968-A 1,8-naphthyridine derivatives useful as anti-bacterial agents DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 1988-04-19 US disclosed
EP-0132845-B1 NOVEL 1,8-NAPHTHYRIDINE DERIVATIVES, AND PROCESS FOR PREPARATION THEREOF Dainippon Pharmaceutical Co., Ltd. (JP) 1988-04-13 EP disclosed
US-4649144-A Antibacterial 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid derivatives DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 1987-03-10 US disclosed
EP-0191451-A1 Novel 1,8-naphthyridine derivatives and processes for preparation thereof Dainippon Pharmaceutical Co., Ltd. (JP) 1986-08-20 EP disclosed
EP-0187376-A2 6,7-Disubstituted 1-cyclopropyl-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids BAYER AG (DE) 1986-07-16 EP disclosed
EP-0160578-A1 1,8-Naphthyridine derivatives DAIICHI SEIYAKU CO., LTD. (JP) 1985-11-06 EP disclosed
EP-0132845-A2 Novel 1,8-Naphthyridine derivatives, and process for preparation thereof Dainippon Pharmaceutical Co., Ltd. (JP) 1985-02-13 EP 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-20260070925-A1 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS NRAS, KRAS, HRAS KEAP1 88/4885NFE2L2 1005/4885ALDH1A1 4329/4885
US-20250302840-A1 COMBINATION THERAPIES MEN1, MLLT1, BMI1 KEAP1 1091/4885NFE2L2 1209/4885ALDH1A1 3293/4885
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS KRAS, NRAS, HRAS KEAP1 47/4885NFE2L2 423/4885ALDH1A1 2204/4885
US-20260132127-A1 NOVEL SPIRO COMPOUND TRHR, NR3C2, THRB KEAP1 911/4885NFE2L2 1705/4885ALDH1A1 1063/4885
US-20260022118-A1 HETEROCYCLIC COMPOUNDS AS NRAS INHIBITORS NRAS, KRAS, HRAS KEAP1 76/4885NFE2L2 1271/4885ALDH1A1 4432/4885

“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.