SCHEMBL358579

SCHEMBL358579

CC(=O)Nc1cc(C)c(Br)cn1

nearest known ligand 0.53

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.53
PTK2 Q05397 1/20 0.46
CRBN Q96SW2 1/20 0.44
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
ABL1 P00519 2/20 0.43
MTOR P42345 1/20 0.43
PIK3C3 Q8NEB9 3/20 0.42
EGFR P00533 1/20 0.42
CYP1A2 P05177 1/20 0.41
GAA P10253 1/20 0.41
GCK P35557 1/20 0.40
KDM4E B2RXH2 1/20 0.40
HSP90AA1 P07900 1/20 0.40
HSP90AB1 P08238 1/20 0.40
NNMT P40261 1/20 0.40
PIK3CG P48736 1/20 0.40
MAP4K1 Q92918 1/20 0.38

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
SCHEMBL3466637 0.87 MTOR (0.43) L3MBTL1NPC1RAB9ASMN1; SMN2ABL1
SCHEMBL624251 0.86 L3MBTL1 (0.53) L3MBTL1PTK2CRBNNPC1RAB9A
SCHEMBL8328931 0.83 L3MBTL1 (0.59) L3MBTL1PTK2CRBNNPC1RAB9A
SCHEMBL4014630 0.83 GAA (0.47) L3MBTL1PTK2NPC1RAB9ASMN1; SMN2
SCHEMBL2026558 0.82 L3MBTL1 (0.53) L3MBTL1PTK2CRBNNPC1RAB9A
SCHEMBL30207707 0.81 CNR2 (0.51) L3MBTL1NPC1RAB9ASMN1; SMN2ABL1
SCHEMBL2731655 0.81 CNR2 (0.51) L3MBTL1NPC1RAB9ASMN1; SMN2ABL1
SCHEMBL20772248 0.81 L3MBTL1 (0.52) L3MBTL1PTK2NPC1RAB9ASMN1; SMN2
SCHEMBL15240729 0.81 PTK2 (0.53) L3MBTL1PTK2NPC1RAB9ASMN1; SMN2
SCHEMBL7936580 0.80 ABL1 (0.43) RAB9AABL1MTORGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101863830-B Synthesis method of 2-amino-5-bromine isonicotinic acid ZHEJIANG CHIMICA LAB CO LTD 2012-07-25 CN claimed
CN-101863830-A Synthesis method of 2-amino-5-bromine isonicotinic acid ZHEJIANG CHIMICA LAB CO LTD 2010-10-20 CN claimed
US-20250340551-A1 SMALL MOLECULE MODULATORS OF STAT6 GILEAD SCIENCES INC (US) 2025-11-06 US disclosed
US-20250325677-A1 STAT6 DEGRADERS GILEAD SCIENCES INC (US) 2025-10-23 US disclosed
US-11935803-B2 Resin composition, laminate, semiconductor wafer with resin composition layer, substrate for mounting semiconductor with resin composition layer and semiconductor device MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2024-03-19 US disclosed
CN-112004845-B Resin composition, laminate, semiconductor wafer with resin composition layer, substrate, and semiconductor device 三菱瓦斯化学株式会社 2022-05-31 CN disclosed
US-20210277221-A1 RESIN COMPOSITION, LAMINATE, SEMICONDUCTOR WAFER WITH RESIN COMPOSITION LAYER, SUBSTRATE FOR MOUNTING SEMICONDUCTOR WITH RESIN COMPOSITION LAYER AND SEMICONDUCTOR DEVICE MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2021-09-09 US disclosed
EP-3786200-A1 RESIN COMPOSITION, LAMINATE, RESIN COMPOSITION LAYER-ATTACHED SEMICONDUCTOR WAFER, SUBSTRATE FOR MOUNTING RESIN COMPOSITION LAYER-ATTACHED SEMICONDUCTOR, AND SEMICONDUCTOR DEVICE MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2021-03-03 EP disclosed
CN-112004845-A Resin composition, laminate, semiconductor wafer with resin composition layer, substrate for mounting semiconductor with resin composition layer, and semiconductor device 三菱瓦斯化学株式会社 2020-11-27 CN disclosed
US-9062046-B2 Substituted imidazoquinoline derivatives as kinase inhibitors Piramal Enterprises Limited (IN) 2015-06-23 US disclosed
CN-103788080-A Isonicotinic acid WUXI VISION PRO LTD 2014-05-14 CN disclosed
US-20090221608-A1 PYRAZOLE COMPOUNDS PFIZER INC. 2009-09-03 US disclosed
US-20090221608-A1 PYRAZOLE COMPOUNDS PFIZER INC. 2009-09-03 US disclosed
WO-2009088103-A1 PYRIDYLAMIDINE COMPOUND OR SALT THEREOF, AND AGRICULTURAL OR HORTICULTURAL FUNGICIDE COMPOSITION CONTAINING THE SAME AS ACTIVE INGREDIENT ISHIHARA SANGYO KAISHA, LTD. (JP) 2009-07-16 WO disclosed
WO-2009016460-A2 PYRAZOLE COMPOUNDS AND THEIR USE AS RAF INHIBITORS PFIZER INC. (US) 2009-02-05 WO disclosed
WO-2009016460-A2 PYRAZOLE COMPOUNDS AND THEIR USE AS RAF INHIBITORS PFIZER INC. (US) 2009-02-05 WO disclosed
EP-0530524-B1 Method of producing 2-amino-3-nitro-5-halogenopyridine ICHIKAWA GOSEI KAGAKU KK (JP) 2003-02-05 EP disclosed
US-5453512-A Bromination of acylaminopyridine with 2-acylaminopyridinium hydorbromide ICHIKAWA GOSEI CHEMICAL CO., LTD. (JP) 1995-09-26 US disclosed
US-5290943-A Halogenation of pyridine compound ICHIKAWA GOSEI CHEMICAL CO., LTD. (JP) 1994-03-01 US disclosed
EP-0530524-A1 Method of producing 2-amino-3-nitro-5-halogenopyridine ICHIKAWA GOSEI CHEMICAL CO., LTD. (JP) 1993-03-10 EP 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 (3 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-20090221608-A1 PYRAZOLE COMPOUNDS BRAF, RAF1, NRAS L3MBTL1 4096/4885PTK2 970/4885CRBN 1130/4885
US-20250325677-A1 STAT6 DEGRADERS STAT6, STAT5B, STAT1 L3MBTL1 2841/4885PTK2 3773/4885CRBN 1627/4885
US-20250340551-A1 SMALL MOLECULE MODULATORS OF STAT6 STAT6, STAT1, STAT5B L3MBTL1 2835/4885PTK2 964/4885CRBN 1488/4885

“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.