SCHEMBL1248489

SCHEMBL1248489

COc1cc(OC)cc(-c2cc3cnc(N)nc3nc2NC(=O)NC(C)(C)C)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ FGFR1 P11362 20/20 1.00
▸ FGFR2 P21802 6/20 1.00
▸ FGFR4 P22455 6/20 1.00
▸ FGFR3 P22607 6/20 1.00
▸ EGFR P00533 4/20 1.00
▸ PDGFRB P09619 10/20 0.83
▸ PDGFRA P16234 10/20 0.83
▸ SRC P12931 7/20 0.82
▸ FLT1 P17948 1/20 0.68
▸ FLT4 P35916 1/20 0.68
▸ KDR P35968 1/20 0.68

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
SCHEMBL29366761 1.00 FGFR1 (1.00) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL8135892 0.90 FGFR1 (1.00) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL8130155 0.86 FGFR1 (1.00) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL22532383 0.85 FGFR1 (0.74) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL29390330 0.85 FGFR1 (0.74) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL8130610 0.84 FGFR1 (1.00) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL8127464 0.83 FGFR1 (0.82) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL30386897 0.82 FGFR1 (0.69) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL31648262 0.82 FGFR1 (0.76) FGFR1FGFR2FGFR4FGFR3EGFR
SCHEMBL8130201 0.82 FGFR1 (1.00) FGFR1FGFR2FGFR4FGFR3EGFR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112313327-B Proliferation inhibitors 千纸鹤治疗公司 2024-04-19 — — CN claimed
US-20210254014-A1 GROWTH INHIBITOR KYOTO UNIVERSITY (JP) 2021-08-19 — — US claimed
EP-3812456-A1 GROWTH INHIBITOR Kyoto University (JP) 2021-04-28 — — EP claimed
CN-112313327-A Proliferation inhibitor 国立大学法人京都大学 2021-02-02 — — CN claimed
US-20100105031-A1 METHOD FOR PREDICTION OF THE EFFICACY OF VASCULARIZATION INHIBITOR ESAI R & D MANAGEMENT CO., LTD. (JP) 2010-04-29 — — US claimed
US-20100092490-A1 METHOD FOR ASSAY ON THE EFFECT OF VASCULARIZATION INHIBITOR EISAI R&D MANAGEMENT CO., LTD. (JP) 2010-04-15 — — US claimed
EP-1925676-A1 METHOD FOR ASSAY ON THE EFFECT OF VASCULARIZATION INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-05-28 — — EP claimed
EP-1925941-A1 METHOD FOR PREDICTION OF THE EFFICACY OF VASCULARIZATION INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-05-28 — — EP claimed
EP-1797877-A1 JOINT USE OF SULFONAMIDE BASED COMPOUND WITH ANGIOGENESIS INHIBITOR Eisai Co., Ltd. (JP) 2007-06-20 — — EP claimed
US-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors EISAI CO., LTD. (JP) 2006-06-22 — — US claimed
US-20260103678-A1 BILAYER OF RETINAL PIGMENTED EPITHELIUM AND PHOTORECEPTORS AND USE THEREOF FUJIFILM Cellular Dynamics, Inc. (US) 2026-04-16 — — US disclosed
US-20260041817-A1 BIODEGRADABLE TISSUE REPLACEMENT IMPLANT AND ITS USE THE U.S.A., AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2026-02-12 — — US disclosed
EP-4680255-A1 METHODS FOR PRODUCING STABLE HUMAN CHONDROCTYES AND THEIR USE FOR PROMOTING CARTILLAGE GROWTH AND REPAIR The United States of America, as represented by the Secretary, Department of Health and Human Services (US) 2026-01-21 — — EP disclosed
EP-4346928-B1 BIODEGRADABLE TISSUE SCAFFOLD WITH SECONDARY MATRIX TO HOST WEAKLY ADHERENT CELLS US HEALTH (US) 2026-01-14 — — EP disclosed
EP-3954436-B1 METHOD FOR PRODUCING BIOTISSUE-LIKE STRUCTURE ORIZURU THERAPEUTICS INC (JP) 2026-01-07 — — EP disclosed
US-20040235870-A1 Enzyme inhibitor contains two or more ligand moieties comprising pyrimidinyl groups covalently linked together by linking groups; keratitis, diabetic retinopathy, angiogenesis, vision defects, ischemia, atherosclerosis,psoriasis, cancer, cirrhosis, diabetes, arthritis, autoimmune disease THERAVANCE BIOPHARMA R&D IP, LLC 2004-11-25 — — US disclosed
US-6750241-B2 Protein kinase inhibitors THERAVANCE, INC. 2004-06-15 — — US disclosed
US-20020177600-A1 Protein kinase inhibitors THERAVANCE BIOPHARMA R&D IP, LLC 2002-11-28 — — US disclosed
US-20020002169-A1 Protein kinase inhibitors THERAVANCE BIOPHARMA R&D IP, LLC 2002-01-03 — — US disclosed
WO-2001042243-A2 PROTEIN KINASE INHIBITORS ADVANCED MEDICINE, INC. (US) 2001-06-14 — — 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-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors FLT4, KDR, FLT1 FGFR1 30/4885FGFR2 62/4885FGFR4 49/4885
US-20020177600-A1 Protein kinase inhibitors MAP3K20, MAP3K9, MAP3K6 FGFR1 797/4885FGFR2 1381/4885FGFR4 2414/4885
US-20260103678-A1 BILAYER OF RETINAL PIGMENTED EPITHELIUM AND PHOTORECEPTORS AND USE THEREOF PAX2, ZP1, ALDH1A2 FGFR1 712/4885FGFR2 1293/4885FGFR4 1109/4885
US-20100092490-A1 METHOD FOR ASSAY ON THE EFFECT OF VASCULARIZATION INHIBITOR VEGFA, FLT4, MKI67 FGFR1 87/4885FGFR2 220/4885FGFR4 70/4885
US-20020002169-A1 Protein kinase inhibitors MAP3K20, MAP3K6, MAP4K2 FGFR1 848/4885FGFR2 1173/4885FGFR4 1995/4885
US-20260041817-A1 BIODEGRADABLE TISSUE REPLACEMENT IMPLANT AND ITS USE LGALS1, LGALS9, ALDH1A2 FGFR1 499/4885FGFR2 1047/4885FGFR4 1593/4885
US-20210254014-A1 GROWTH INHIBITOR MKI67, FGFR1, FGF2 FGFR1 2/4885FGFR2 4/4885FGFR4 7/4885
US-20040235870-A1 Enzyme inhibitor contains two or more ligand moieties comprising pyrimidinyl groups covalently linked together by linking groups; keratitis, diabetic retinopathy, angiogenesis, vision defects, ischemia, atherosclerosis,psoriasis, cancer, cirrhosis, diabetes, arthritis, autoimmune disease UACA, PRKDC, CDK2 FGFR1 739/4885FGFR2 1138/4885FGFR4 950/4885

“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.

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