SCHEMBL2961144

SCHEMBL2961144

CC(C)(C)n1nc(Br)c2c(N)ncnc21

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SRC P12931 12/20 0.58
ABL1 P00519 7/20 0.58
RET P07949 5/20 0.57
PRKD3 O94806 5/20 0.57
PRKD2 Q9BZL6 5/20 0.57
KDR P35968 4/20 0.57
RIPK2 O43353 3/20 0.57
FYN P06241 3/20 0.57
CSNK1D P48730 3/20 0.57
EGFR P00533 3/20 0.57
KDM4E B2RXH2 2/20 0.57
ALDH1A1 P00352 2/20 0.57
LMNA P02545 2/20 0.57
LCK P06239 2/20 0.57
YES1 P07947 2/20 0.57
LYN P07948 2/20 0.57
PDGFRA P16234 2/20 0.57
PRKACA P17612 2/20 0.57
FRK P42685 2/20 0.57
HTT P42858 2/20 0.57

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
SCHEMBL13019650 0.83 SRC (0.64) SRCABL1RETPRKD3PRKD2
SCHEMBL15929311 0.80 SRC (0.61) SRCABL1RETPRKD3PRKD2
SCHEMBL3782929 0.80 SRC (0.58) SRCABL1RETPRKD3PRKD2
SCHEMBL22521563 0.80 KDM4E (0.63) SRCABL1RETPRKD3PRKD2
SCHEMBL15471369 0.80 SRC (0.58) SRCABL1RETPRKD3PRKD2
SCHEMBL23055859 0.80 SRC (0.58) SRCABL1RETPRKD3PRKD2
SCHEMBL13019664 0.79 SRC (0.57) SRCABL1RETPRKD3PRKD2
SCHEMBL14617301 0.78 SRC (0.89) SRCABL1RETPRKD3PRKD2
SCHEMBL24735059 0.78 SRC (0.56) SRCABL1RETPRKD3PRKD2
SCHEMBL3788404 0.78 SRC (0.57) SRCABL1RETPRKD3PRKD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250243202-A1 Compounds Useful as RET Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2025-07-31 US disclosed
US-20250236624-A1 Heterocyclic Compounds as RET Kinase Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2025-07-24 US disclosed
WO-2025137605-A1 COMPOUNDS FOR TARGETED DEGRADATION OF PROTO-ONCOGENE TYROSINE PROTEIN KINASE RECEPTOR C4 THERAPEUTICS, INC. (US) 2025-06-26 WO disclosed
CN-115785100-B Compounds useful as RET inhibitors 癌症研究科技有限公司 2025-01-07 CN disclosed
CN-117958271-B Benzoxazole-like compounds and their use for the preparation of products for increasing plant resistance by closing stomata 北京大学现代农业研究院 2024-08-13 CN disclosed
CN-115650985-B Heterocyclic compounds as RET kinase inhibitors 癌症研究科技有限公司 2024-08-02 CN disclosed
CN-117958271-A Benzoxazole-like compounds and their use in the preparation of products for increasing plant resistance by closing stomata 北京大学现代农业研究院 2024-05-03 CN disclosed
US-20240132504-A1 Compounds Useful as RET Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2024-04-25 US disclosed
US-20240116938-A1 Heterocyclic Compounds as RET Kinase Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2024-04-11 US disclosed
US-20230339954-A1 Heterocyclic Compounds as RET Kinase Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2023-10-26 US disclosed
WO-2009062118-A2 MODULATION OF PROTEIN TRAFFICKING FOLDRX PHARMACEUTICALS, INC. (US) 2009-05-14 WO disclosed
EP-2007373-A2 INHIBITION OF ALPHA-SYNUCLEIN TOXICITY Foldrx Pharmaceuticals, Inc. (US) 2008-12-31 EP disclosed
EP-1973917-A2 PROTEIN KINASE INHIBITORS Abbott Laboratories (US) 2008-10-01 EP disclosed
WO-2007126841-A2 INHIBITION OF ALPHA-SYNUCLEIN TOXICITY FOLDRX PHARMACEUTICALS, INC. (US) 2007-11-08 WO disclosed
WO-2007126841-A2 INHIBITION OF ALPHA-SYNUCLEIN TOXICITY FOLDRX PHARMACEUTICALS, INC. (US) 2007-11-08 WO disclosed
US-20070203143-A1 PROTEIN KINASE INHIBITORS ABBVIE INC. 2007-08-30 US disclosed
WO-2007079164-A2 PROTEIN KINASE INHIBITORS ABBOTT LABORATORIES (US) 2007-07-12 WO disclosed
EP-1730148-A2 AMINOBENZOXAZOLES AS THERAPEUTIC AGENTS Abbott Laboratories (US) 2006-12-13 EP disclosed
US-20060025383-A1 Aminobenzoxazoles as therapeutic agents ABBOTT LABORATORIES 2006-02-02 US disclosed
WO-2005074603-A2 AMINOBENZOXAZOLES AS THERAPEUTIC AGENTS ABBOTT LABORATORIES (US) 2005-08-18 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 (7 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-20060025383-A1 Aminobenzoxazoles as therapeutic agents ABL1, MAP3K19, MAP3K20 SRC 116/4885ABL1 1/4885RET 848/4885
US-20250236624-A1 Heterocyclic Compounds as RET Kinase Inhibitors RET, REL, BCR SRC 21/4885ABL1 23/4885RET 1/4885
US-20250243202-A1 Compounds Useful as RET Inhibitors RET, BCR, REL SRC 23/4885ABL1 25/4885RET 1/4885
US-20230339954-A1 Heterocyclic Compounds as RET Kinase Inhibitors RET, REL, BCR SRC 21/4885ABL1 23/4885RET 1/4885
US-20240132504-A1 Compounds Useful as RET Inhibitors RET, BCR, REL SRC 23/4885ABL1 25/4885RET 1/4885
US-20240116938-A1 Heterocyclic Compounds as RET Kinase Inhibitors RET, HIPK4, HIPK3 SRC 24/4885ABL1 13/4885RET 1/4885
US-20070203143-A1 PROTEIN KINASE INHIBITORS PACSIN2, MAP3K20, PHKG1 SRC 106/4885ABL1 60/4885RET 510/4885

“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.