SCHEMBL12428872

SCHEMBL12428872

CNC(=O)c1c(F)cccc1Nc1nc(Nc2cc3c(cc2OC)CCN3C(=O)CN(C)C)nc2[nH]ccc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ IGF1R P08069 20/20 1.00
▸ MAPK8 P45983 16/20 1.00
▸ ALK Q9UM73 3/20 1.00
▸ DAPK3 O43293 2/20 1.00
▸ PRKD3 O94806 2/20 1.00
▸ ROS1 P08922 2/20 1.00
▸ FER P16591 2/20 1.00
▸ LTK P29376 2/20 1.00
▸ AXL P30530 2/20 1.00
▸ MAPK9 P45984 2/20 1.00
▸ CLK2 P49760 2/20 1.00
▸ RPS6KA3 P51812 2/20 1.00
▸ CSNK2A1 P68400 2/20 1.00
▸ PTK2 Q05397 2/20 1.00
▸ LRRK2 Q5S007 2/20 1.00
▸ TAOK1 Q7L7X3 2/20 1.00
▸ HIPK4 Q8NE63 2/20 1.00
▸ CLK4 Q9HAZ1 2/20 1.00
▸ DYRK1B Q9Y463 2/20 1.00
▸ INSR P06213 2/20 1.00

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
SCHEMBL29410234 1.00 IGF1R (1.00) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL30197710 1.00 IGF1R (1.00) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL29355553 1.00 IGF1R (1.00) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL12429998 0.97 IGF1R (0.95) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL12428871 0.96 IGF1R (0.93) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL12429882 0.95 IGF1R (0.90) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL18719947 0.95 IGF1R (0.90) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL12429889 0.94 IGF1R (0.88) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL12429891 0.94 IGF1R (0.88) IGF1RMAPK8ALKDAPK3PRKD3
SCHEMBL12429838 0.94 IGF1R (0.88) IGF1RMAPK8ALKDAPK3PRKD3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250333479-A1 NOVEL FUSION MOLECULES AND USES THEREOF FOUNDATION MEDICINE, INC. (US) 2025-10-30 — — US disclosed
US-20250333480-A1 FUSION MOLECULES AND USES THEREOF FOUNDATION MEDICINE, INC. (US) 2025-10-30 — — US disclosed
US-20240360199-A1 NOVEL FUSION MOLECULES AND USES THEREOF FOUNDATION MEDICINE, INC. (US) 2024-10-31 — — US disclosed
CN-118318033-A Cell aggregate comprising pituitary hormone-producing cells and method for producing the same 住友制药株式会社 2024-07-09 — — CN disclosed
CN-118043447-A Method for preparing cell population containing pituitary tissue and cell population 住友化学株式会社 2024-05-14 — — CN disclosed
US-11771709-B2 ALK protein degradation agent and anti-tumor application thereof SHANGHAITECH UNIVERSITY (CN) 2023-10-03 — — US disclosed
EP-4223770-A2 NOVEL FUSION MOLECULES AND USES THEREOF Foundation Medicine, Inc. (US) 2023-08-09 — — EP disclosed
US-20220169703-A1 NOVEL FUSION MOLECULES AND USES THEREOF FOUNDATION MEDICINE, INC. (US) 2022-06-02 — — US disclosed
US-20220169703-A1 NOVEL FUSION MOLECULES AND USES THEREOF FOUNDATION MEDICINE, INC. (US) 2022-06-02 — — US disclosed
US-20220117982-A1 TARGET PROTEIN DEGRADATION COMPOUNDS, THEIR ANTI-TUMOR USE, THEIR INTERMEDIATES AND USE OF INTERMEDIATES SHANGHAITECH UNIVERSITY (CN) 2022-04-21 — — US disclosed
US-20150374767-A1 Treatment of Cancer VIRTTU BIOLOGICS LIMITED (GB) 2015-12-31 — — US disclosed
WO-2015144808-A1 COMBINATIONS OF AN FGFR INHIBITOR AND AN IGF1R INHIBITOR ASTEX THERAPEUTICS LTD (GB) 2015-10-01 — — WO disclosed
WO-2014175444-A1 ANTI-NLRR1 ANTIBODY 千葉県 (JP) 2014-10-30 — — WO disclosed
WO-2014128487-A1 TREATMENT OF CANCER VIRTTU BIOLOGICS LIMITED (GB) 2014-08-28 — — WO disclosed
EP-2188292-B1 2- [ (2-{PHENYLAMINO}-1H-PYRROLO [2, 3-D]PYRIMIDIN-4-YL) AMINO]BENZAMIDE DERIVATIVES AS IGF-1R INHIBITORS FOR THE TREATMENT OF CANCER GLAXOSMITHKLINE IP DEV LTD (GB) 2013-05-29 — — EP disclosed
US-7981903-B2 2-[2-{phenylamino}-1H-pyrrolo[2,3-D]pyrimidin-4-yl)amino] benzamide derivatives as IGF-1R inhibitors for the treatment of cancer GLAXOSMITHKLINE LLC (US) 2011-07-19 — — US disclosed
US-7981903-B2 2-[2-{phenylamino}-1H-pyrrolo[2,3-D]pyrimidin-4-yl)amino] benzamide derivatives as IGF-1R inhibitors for the treatment of cancer GLAXOSMITHKLINE LLC (US) 2011-07-19 — — US disclosed
US-20100204196-A1 2-[2--1H-Pyrrolo[2,3-D]Pyrimidin-4-YL)Amino] Benzamide Derivatives As IGF-1R Inhibitors For The Treatment Of Cancer GLAXOSMITHKLINE LLC 2010-08-12 — — US disclosed
US-20100204196-A1 2-[2--1H-Pyrrolo[2,3-D]Pyrimidin-4-YL)Amino] Benzamide Derivatives As IGF-1R Inhibitors For The Treatment Of Cancer GLAXOSMITHKLINE LLC 2010-08-12 — — US disclosed
WO-2009020990-A1 2- [ (2-{PHENYLAMINO}-1H-PYRROLO [2, 3-D] PYRIMIDIN-4-YL) AMINO] BENZAMIDE DERIVATIVES AS IGF-1R INHIBITORS FOR THE TREATMENT OF CANCER SMITHKLINE BEECHAM CORPORATION (US) 2009-02-12 — — 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-20150374767-A1 Treatment of Cancer EGFR, ERBB2, MET IGF1R 27/4885MAPK8 518/4885ALK 33/4885
US-20220169703-A1 NOVEL FUSION MOLECULES AND USES THEREOF RPS27A, CD2BP2, FGB IGF1R 3025/4885MAPK8 4038/4885ALK 200/4885
US-20240360199-A1 NOVEL FUSION MOLECULES AND USES THEREOF RPS27A, CD2BP2, FGB IGF1R 3025/4885MAPK8 4038/4885ALK 200/4885
US-20100204196-A1 2-[2--1H-Pyrrolo[2,3-D]Pyrimidin-4-YL)Amino] Benzamide Derivatives As IGF-1R Inhibitors For The Treatment Of Cancer IGF1R, IGFBP2, IGFBP1 IGF1R 1/4885MAPK8 1305/4885ALK 285/4885
US-20250333479-A1 NOVEL FUSION MOLECULES AND USES THEREOF RPS27A, CD2BP2, FGB IGF1R 3025/4885MAPK8 4038/4885ALK 200/4885
US-11771709-B2 ALK protein degradation agent and anti-tumor application thereof ADRM1, VHL, MDM2 IGF1R 306/4885MAPK8 1053/4885ALK 5/4885
US-20220117982-A1 TARGET PROTEIN DEGRADATION COMPOUNDS, THEIR ANTI-TUMOR USE, THEIR INTERMEDIATES AND USE OF INTERMEDIATES UFM1, SUMO1, SUMO2 IGF1R 1585/4885MAPK8 1903/4885ALK 2497/4885
US-20250333480-A1 FUSION MOLECULES AND USES THEREOF RPS27A, CD2BP2, FGB IGF1R 3166/4885MAPK8 4114/4885ALK 171/4885

“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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