SCHEMBL177518

SCHEMBL177518

CNC(=O)c1cc(Cl)ccn1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4C Q9H3R0 1/20 0.62
ALDH1A1 P00352 1/20 0.54
MAPT P10636 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
RAB9A P51151 5/20 0.54
NPC1 O15118 4/20 0.54
CASP3 P42574 1/20 0.50
SENP8 Q96LD8 1/20 0.50
SENP7 Q9BQF6 1/20 0.50
SENP6 Q9GZR1 1/20 0.50
GRM5 P41594 2/20 0.48
GAA P10253 1/20 0.46
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
KDR P35968 2/20 0.46
RAF1 P04049 1/20 0.46
SCN10A Q9Y5Y9 1/20 0.46
GRM4 Q14833 1/20 0.45
HDAC6 Q9UBN7 1/20 0.45
CYP1A2 P05177 1/20 0.45

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
SCHEMBL30155195 1.00 KDM4C (0.62) KDM4CALDH1A1MAPTL3MBTL1RAB9A
Hydrochloric Acid SCHEMBL700397 0.98 KDM4C (0.60) KDM4CALDH1A1MAPTL3MBTL1RAB9A
SCHEMBL14480939 0.88 KDM4C (0.57) KDM4CALDH1A1MAPTL3MBTL1RAB9A
Tetrahydrofuran SCHEMBL28241044 0.88 KDM4C (0.51) KDM4CALDH1A1MAPTL3MBTL1RAB9A
SCHEMBL28426040 0.84 ALDH1A1 (0.51) KDM4CALDH1A1MAPTL3MBTL1RAB9A
SCHEMBL18135104 0.83 GAA (0.56) KDM4CRAB9AGRM5GAAMEN1
SCHEMBL6386120 0.82 KDM4C (0.52) KDM4CALDH1A1MAPTL3MBTL1RAB9A
SCHEMBL1054692 0.81 KDM4C (0.58) KDM4CALDH1A1MAPTL3MBTL1RAB9A
SCHEMBL163711 0.81 KDR (0.48) KDM4CALDH1A1MAPTRAB9ANPC1
SCHEMBL25992871 0.81 KDR (0.51) KDM4CRAB9ANPC1GRM5GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120082897-A Preparation method for electrochemically synthesizing N-substituted pyridine-2-formamide 九洲药业(杭州)有限公司 2025-06-03 CN claimed
CN-119241427-A Method for comprehensively and efficiently synthesizing anticancer drug regorafenib 董帅圻 2025-01-03 CN claimed
CN-118108667-A Preparation method of regorafenib 南京法恩化学有限公司 2024-05-31 CN claimed
CN-114957111-B Preparation method of N-methyl-4-chloropyridine-2-formamide 扬州市普林斯医药科技有限公司 2024-02-09 CN claimed
CN-117447395-A Method for preparing sorafenib key intermediate by utilizing micro-channel continuous flow 山东安弘制药有限公司 2024-01-26 CN claimed
CN-117285460-A Method for preparing regorafenib intermediate by using continuous flow reaction technology 重庆药友制药有限责任公司 2023-12-26 CN claimed
CN-114957111-A Preparation method of N-methyl-4-chloropyridine-2-formamide 扬州市普林斯医药科技有限公司 2022-08-30 CN claimed
CN-114539141-A Preparation method of sorafenib 南京焕然生物科技有限公司 2022-05-27 CN claimed
US-10822305-B2 Process for the preparation of 4-(4-amino-3-fluorophenoxy)-N-methylpyyridine-2-carboxamide BAYER HEALTHCARE LLC (US) 2020-11-03 US claimed
CN-108997209-B Preparation method of regorafenib 山东罗欣药业集团恒欣药业有限公司 2020-08-04 CN claimed
WO-2015049698-A2 PROCESS FOR REGORAFENIB HETERO RESEARCH FOUNDATION (IN) 2015-04-09 WO claimed
US-20130210865-A1 SORAFENIB DIMETHYL SULPHOXIDE SOLVATE RANBAXY LABORATORIES LIMITED (IN) 2013-08-15 US claimed
US-8445687-B2 Process for the preparation of a RAF kinase inhibitor and intermediates for use in the process CIPLA LIMITED (IN) 2013-05-21 US claimed
EP-2528899-A2 SORAFENIB DIMETHYL SULPHOXIDE SOLVATE Ranbaxy Laboratories Limited (IN) 2012-12-05 EP claimed
CN-102311384-A Preparation method of sorafenib XIANGZHEN BIOTECHNOLOGY CO LTD 2012-01-11 CN claimed
WO-2011092663-A2 4-(4-{3-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]UREIDO}PHENOXY)-N2-METHYLPYRIDINE-2-CARBOXAMIDE DIMETHYL SULPHOXIDE SOLVATE RANBAXY LABORATORIES LIMITED (IN) 2011-08-04 WO claimed
US-20100311980-A1 Process for the Preparation of a RAF Kinase Inhibitor and Intermediates for Use in the Process CIPLA LIMITED (IN) 2010-12-09 US claimed
EP-2195286-A2 PROCESS FOR THE PREPARATION OF A RAF KINASE INHIBITOR AND INTERMEDIATES FOR USE IN THE PROCESS Cipla Limited (IN) 2010-06-16 EP claimed
WO-2009034308-A2 PROCESS FOR THE PREPARATION OF A RAF KINASE INHIBITOR AND INTERMEDIATES FOR USE IN THE PROCESS CIPLA LIMITED (IN) 2009-03-19 WO claimed
CN-101302193-A Entironment-friendly preparation of sorafenib intermediate SHANGHAI HWASUN LIFE SCIENCE C (CN) 2008-11-12 CN claimed

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-20130210865-A1 SORAFENIB DIMETHYL SULPHOXIDE SOLVATE SRMS, SRM, BRAF KDM4C 114/4885ALDH1A1 796/4885MAPT 2270/4885
US-20100311980-A1 Process for the Preparation of a RAF Kinase Inhibitor and Intermediates for Use in the Process BRAF, RAF1, ARAF KDM4C 2789/4885ALDH1A1 2911/4885MAPT 3477/4885
US-10822305-B2 Process for the preparation of 4-(4-amino-3-fluorophenoxy)-N-methylpyyridine-2-carboxamide DNPEP, NPEPPS, TET3 KDM4C 10/4885ALDH1A1 1840/4885MAPT 683/4885

“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.