SCHEMBL3727488

SCHEMBL3727488

COc1cc2nc(N(Cl)c3ccc(F)cc3)ncc2cc1OCCCN1CCOCC1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ EGFR P00533 11/20 0.49
▸ EHMT2 Q96KQ7 1/20 0.48
▸ EHMT1 Q9H9B1 1/20 0.48
▸ KDR P35968 4/20 0.46
▸ SRC P12931 3/20 0.46
▸ FLT4 P35916 2/20 0.46
▸ AXL P30530 2/20 0.46
▸ ERBB2 P04626 2/20 0.46
▸ MET P08581 2/20 0.46
▸ KIT P10721 2/20 0.46
▸ CIT O14578 1/20 0.46
▸ GAK O14976 1/20 0.46
▸ EPHB6 O15197 1/20 0.46
▸ ABCC4 O15439 1/20 0.46
▸ DAPK3 O43293 1/20 0.46
▸ RIPK2 O43353 1/20 0.46
▸ NR1I2 O75469 1/20 0.46
▸ RPS6KA4 O75676 1/20 0.46
▸ STK17B O94768 1/20 0.46
▸ STK10 O94804 1/20 0.46

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
SCHEMBL6266570 0.96 EGFR (0.46) EGFREHMT2EHMT1KDRSRC
SCHEMBL6268116 0.92 EHMT2 (0.57) EHMT2EHMT1TLR9TLR7
SCHEMBL5618725 0.87 EHMT2 (0.51) EGFREHMT2EHMT1KDREPHB4
SCHEMBL8438071 0.82 KDR (0.38) EGFREHMT2EHMT1KDRMET
SCHEMBL6269488 0.81 EGFR (0.42) EGFREHMT2EHMT1AXLRET
SCHEMBL8436900 0.81 EPHA2 (0.42) EHMT2EHMT1KDRMETCHEK2
SCHEMBL5084456 0.81 EGFR (0.67) EGFRKDRSRCFLT4AXL
SCHEMBL6266311 0.80 EGFR (0.44) EGFREHMT2EHMT1KDRERBB2
SCHEMBL8444662 0.80 EPHA2 (0.44) EHMT2EHMT1KDRCHEK2EPHB4
SCHEMBL27607881 0.79 KDM4E (0.58) EGFREHMT2EHMT1KDRSRC

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118076612-A Sulfur-containing heteroaromatic tricyclic KRAS inhibitors 医睿世康药业研发公司 2024-05-24 — — CN disclosed
CN-117940452-A Methods and compositions for treating cancer 基因泰克公司 2024-04-26 — — CN disclosed
CN-111936857-B Reagents and methods for predicting response to therapy 艾比克斯治疗私人有限公司 2024-04-16 — — CN disclosed
CN-117715936-A Methods and compositions for treating cancer 豪夫迈·罗氏有限公司 2024-03-15 — — CN disclosed
CN-112805267-B Carboxamide and sulfonamide derivatives as TEAD modulators 豪夫迈·罗氏有限公司 2024-03-08 — — CN disclosed
CN-117545857-A Methods and compositions for the treatment and diagnosis of cancer 基因泰克公司 2024-02-09 — — CN disclosed
CN-117440826-A Administration of treatment with anti-CD 20/anti-CD 3 bispecific antibodies 基因泰克公司 2024-01-23 — — CN disclosed
CN-114867494-B9 anti-LY 6G6D antibodies and methods of use 基因泰克公司 2024-01-12 — — CN disclosed
CN-111213059-B Diagnostic and therapeutic methods for cancer 豪夫迈·罗氏有限公司 2024-01-09 — — CN disclosed
CN-117321078-A Administration for combination therapy with anti-CD 20/anti-CD 3 bispecific antibody and anti-CD 79B antibody drug conjugates 豪夫迈·罗氏有限公司 2023-12-29 — — CN disclosed
WO-2016036873-A1 THERAPEUTIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2016-03-10 — — WO disclosed
WO-2013007765-A1 FUSED TRICYCLIC COMPOUNDS FOR USE AS INHIBITORS OF JANUS KINASES F. HOFFMANN-LA ROCHE AG (CH) 2013-01-17 — — WO disclosed
EP-2242493-A1 DERIVATIVES OF GEFITINIB Concert Pharmaceuticals Inc. (US) 2010-10-27 — — EP disclosed
WO-2009094216-A1 DERIVATIVES OF GEFITINIB CONCERT PHARMACEUTICALS INC. (US) 2009-07-30 — — WO disclosed
WO-2005065074-A2 PROTECTION OF TISSUES AND CELLS FROM CYTOTOXIC EFFECTS OF IONIZING RADIATION BY ABL INHIBITORS TEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2005-07-21 — — WO disclosed
EP-1546119-A1 PROCESS FOR THE PREPARATION OF 4- (3'CHLORO-4'-FLUOROANILINO) -7-METHOXY-6- (3-MORPHOLINOPROPOXY) QUINAZOLINE AstraZeneca AB (SE) 2005-06-29 — — EP disclosed
EP-1480650-A1 NOVEL CRYSTALLINE FORMS OF THE ANTI-CANCER COMPOUND ZD1839 AstraZeneca AB (SE) 2004-12-01 — — EP disclosed
WO-2004024703-A1 PROCESS FOR THE PREPARATION OF 4- (3’-CHLORO-4’-FLUOROANILINO) -7-METHOXY-6- (3-MORPHOLINOPROPOXY) QUINAZOLINE ASTRAZENECA AB (SE) 2004-03-25 — — WO disclosed
WO-2003072108-A1 NOVEL CRYSTALLINE FORMS OF THE ANTI-CANCER COMPOUND ZD1839 ASTRAZENECA AB (SE) 2003-09-04 — — WO disclosed
US-5770599-A RECEPTOR TYROSINE KINASE INHIBITORS including 4-(3'-chloro-4'-fluoroanilino)-7-methoxy-6-(2-morpholinoethoxy)quinazoline (gefitinib) ZENECA LIMITED (GB) 1998-06-23 — — US disclosed
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