Gsk2256294

Gsk2256294

SCHEMBL29557121

CNc1nc(C)nc(N[C@H]2CCC[C@@H](C(=O)NCc3ccc(C#N)cc3C(F)(F)F)C2)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

EPHX2

The experimentally established mechanism targets of Gsk2256294. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
EPHX2 known ✓ P34913 20/20 1.00
CYP2C9 P11712 6/20 0.49
CYP3A4 P08684 2/20 0.47
CYP2D6 P10635 1/20 0.47

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
Gsk2256294 SCHEMBL2677671 1.00 EPHX2 (1.00) EPHX2CYP2C9CYP3A4CYP2D6
Gsk2256294 SCHEMBL2677673 1.00 EPHX2 (1.00) EPHX2CYP2C9CYP3A4CYP2D6
Gsk2256294 SCHEMBL2677667 1.00 EPHX2 (1.00) EPHX2CYP2C9CYP3A4CYP2D6
Gsk2256294 SCHEMBL29667411 1.00 EPHX2 (1.00) EPHX2CYP2C9CYP3A4CYP2D6
Gsk2256294 SCHEMBL30216212 1.00 EPHX2 (1.00) EPHX2CYP2C9CYP3A4CYP2D6
SCHEMBL2677883 0.89 EPHX2 (0.80) EPHX2CYP2C9CYP3A4CYP2D6
SCHEMBL2677886 0.89 EPHX2 (0.80) EPHX2CYP2C9CYP3A4CYP2D6
SCHEMBL2677878 0.89 EPHX2 (0.80) EPHX2CYP2C9CYP3A4CYP2D6
SCHEMBL2678417 0.88 EPHX2 (0.79) EPHX2CYP2C9CYP3A4CYP2D6
SCHEMBL2676508 0.88 EPHX2 (0.79) EPHX2CYP2C9CYP3A4CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12485107-B2 Methods for the prevention or treatment of cytokine storm BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2025-12-02 US claimed
WO-2024105225-A1 SYNERGISTIC COMBINATIONS OF A SIGMA RECEPTOR 1 (S1R) ANTAGONIST AND A SOLUBLE EPOXIDE HYDROLASE INHIBITOR (SEHI) AND THEIR USE IN THE TREATMENT OF PAIN UNIVERSITAT DE BARCELONA (ES) 2024-05-23 WO claimed
US-20240082211-A1 SOLUBLE EPOXIDE HYDROLASE AS A TARGET FOR OCULAR DISEASES INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION 2024-03-14 US claimed
US-20230375561-A1 METHODS FOR IDENTIFICATION, STRATIFICATION, AND TREATMENT OF CNS DISEASES KADDURAH DAOUK RIMA F (US) 2023-11-23 US claimed
WO-2022081350-A2 METHODS FOR IDENTIFICATION, STRATIFICATION, AND TREATMENT OF CNS DISEASES DUKE UNIVERSITY (US) 2022-04-21 WO claimed
US-20260109724-A1 ANTIVIRAL COMPOUNDS GILEAD SCIENCES INC (US) 2026-04-23 US disclosed
US-20260083718-A1 PIPERIDINE UREA DERIVATIVES FOR OBESITY THERAPY ASTRIZI BIO, INC. (US) 2026-03-26 US disclosed
EP-4359402-B1 IMIDAZOLO INDAZOLE COMPOUNDS AS JAK INHIBITORS THERAVANCE BIOPHARMA R&D IP LLC (US) 2026-03-11 EP disclosed
EP-4665737-A1 PHOSPHOLIPID COMPOUNDS AND METHODS OF MAKING AND USING THE SAME GILEAD SCIENCES, INC. (US) 2025-12-24 EP disclosed
EP-4107164-B1 ANTIVIRAL COMPOUNDS GILEAD SCIENCES INC (US) 2025-12-03 EP disclosed
US-12485107-B2 Methods for the prevention or treatment of cytokine storm BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2025-12-02 US disclosed
EP-4644394-A2 ANTIVIRAL COMPOUNDS Gilead Sciences, Inc. (US) 2025-11-05 EP disclosed
CN-115087659-A Antiviral compounds 吉利德科学公司 2022-09-20 CN disclosed
US-20220289737-A1 FUSED IMIDAZO-PIPERIDINE JAK INHIBITORS THERAVANCE BIOPHARMA R&D IP, LLC (US) 2022-09-15 US disclosed
US-11426385-B2 Methods of improving cancer chemotherapy THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2022-08-30 US disclosed
WO-2022178215-A1 AMINO AMIDE TETRAHYDRO IMIDAZO PYRIDINES AS JAK INHIBITORS THERAVANCE BIOPHARMA R&D IP, LLC (US) 2022-08-25 WO disclosed
CN-110461839-B JAK inhibitors containing 4-membered heterocyclic amides 施万生物制药研发IP有限责任公司 2022-08-23 CN disclosed
US-20220218667-A1 DUAL INHIBITORS OF SOLUBLE EPOXIDE HYDROLASE AND METHODS OF USE THEREOF OROX BIOSCIENCES, INC. 2022-07-14 US disclosed
CN-110382498-B Fused imidazole-piperidine JAK inhibitors 施万生物制药研发IP有限责任公司 2022-07-12 CN disclosed
WO-2022081350-A2 METHODS FOR IDENTIFICATION, STRATIFICATION, AND TREATMENT OF CNS DISEASES DUKE UNIVERSITY (US) 2022-04-21 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 (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-20240082211-A1 SOLUBLE EPOXIDE HYDROLASE AS A TARGET FOR OCULAR DISEASES EPHX1, ALDH1A2, EPHX2 EPHX2 3/4885CYP2C9 3672/4885CYP3A4 3461/4885
US-20260109724-A1 ANTIVIRAL COMPOUNDS IRF3, IFNAR1, HAVCR2 EPHX2 3400/4885CYP2C9 1733/4885CYP3A4 155/4885
US-20260083718-A1 PIPERIDINE UREA DERIVATIVES FOR OBESITY THERAPY GLP1R, GIPR, GPR119 EPHX2 3283/4885CYP2C9 2341/4885CYP3A4 2493/4885
US-20220289737-A1 FUSED IMIDAZO-PIPERIDINE JAK INHIBITORS JAK2, JAK1, JAK3 EPHX2 3237/4885CYP2C9 1268/4885CYP3A4 1555/4885
US-12485107-B2 Methods for the prevention or treatment of cytokine storm TNF, PTGES2, IL2 EPHX2 13/4885CYP2C9 1964/4885CYP3A4 1578/4885
US-11426385-B2 Methods of improving cancer chemotherapy ALOX5, EPHX1, ALOX12 EPHX2 10/4885CYP2C9 213/4885CYP3A4 373/4885
US-20230375561-A1 METHODS FOR IDENTIFICATION, STRATIFICATION, AND TREATMENT OF CNS DISEASES SLC25A20, CPT2, NDUFAB1 EPHX2 1139/4885CYP2C9 949/4885CYP3A4 1119/4885
US-20220218667-A1 DUAL INHIBITORS OF SOLUBLE EPOXIDE HYDROLASE AND METHODS OF USE THEREOF PTGES2, PTGS2, PTGES3 EPHX2 4/4885CYP2C9 1732/4885CYP3A4 1545/4885

“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.