SCHEMBL1014289

SCHEMBL1014289

CC(C)Sc1ccccc1N

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.54
KMT2A Q03164 4/20 0.54
NPSR1 Q6W5P4 4/20 0.54
MEN1 O00255 3/20 0.54
APOBEC3G Q9HC16 2/20 0.54
TDP1 Q9NUW8 4/20 0.49
KDM4E B2RXH2 2/20 0.49
MAP2K1 Q02750 3/20 0.44
POLB P06746 1/20 0.43
MAPK1 P28482 2/20 0.42
CYP3A4 P08684 3/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
ALOX15 P16050 2/20 0.41
CASP1 P29466 1/20 0.41
CASP7 P55210 1/20 0.41
SLC6A2 P23975 1/20 0.40
SLC6A4 P31645 1/20 0.40
SLC6A3 Q01959 1/20 0.40
CYP1A2 P05177 1/20 0.39
CYP2C9 P11712 1/20 0.39

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
Hydrochloric Acid SCHEMBL19896479 0.98 MAPT (0.52) MAPTKMT2ANPSR1MEN1APOBEC3G
Aniline SCHEMBL22169182 0.92 MAPT (0.47) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL540557 0.86 MAPT (0.54) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL17879577 0.82 MAPT (0.50) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL30548758 0.82 MAP2K7 (0.41) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL11375178 0.80 MAPT (0.48) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL11385640 0.79 MAPT (0.46) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL22085893 0.79 ALDH1A1 (0.38) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL11099046 0.79 MAPT (0.46) MAPTKMT2ANPSR1MEN1APOBEC3G
SCHEMBL11177994 0.77 MAPT (0.45) MAPTKMT2ANPSR1MEN1APOBEC3G

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2017041771-A1 PROCESS FOR THE PREPARATION OF CERITINIB USING \"IN SITU\" PREPARED 5-METHYL-2-(1 -METHYLETHOXY)-4-(4-PIPERIDINYL)-BENZENAMINE MONOHYDROCHLORIDE (1 :1 ) AS AN INTERMEDIATE ZENTIVA, K.S. (CZ) 2017-03-16 WO claimed
CN-116284001-A DCLK1 inhibitor, preparation method, pharmaceutical composition and application 中国药科大学 2023-06-23 CN disclosed
WO-2022214008-A1 HIGHLY ACTIVE HPK1 KINASE INHIBITOR 杭州阿诺生物医药科技有限公司 2022-10-13 WO disclosed
EP-2985284-B1 DICARBOXYLIC ACID BISAMIDE DERIVATIVES, USE THEREOF, PHARMACEUTICAL COMPOSITION BASED THEREON AND METHODS FOR PRODUCING DICARBOXYLIC ACID BISAMIDE DERIVATIVES TREAMID THERAPEUTICS GMBH (DE) 2021-11-03 EP disclosed
WO-2021057867-A1 CLASS OF CDK INHIBITOR BASED ON ORGANIC ARSINE, PREPARATION METHOD AND APPLICATION THEREOF 中国科学院上海有机化学研究所 2021-04-01 WO disclosed
EP-3265455-B1 PROCESS FOR PREPARING CERITINIB AND INTERMEDIATES THEREOF NOVARTIS AG (CH) 2020-07-15 EP disclosed
US-10618884-B2 Deuterated diaminopyrimidine compounds and pharmaceutical compositions comprising such compounds SUZHOU ZELGEN BIOPHARMACEUTICALS CO., LTD. (CN) 2020-04-14 US disclosed
US-20200039935-A1 Chemical Process for Preparing Pyrimidine Derivatives and Intermediates Thereof SUZHOU NOVARTIS PHARMA TECHNOLOGY CO., LTD (CN) 2020-02-06 US disclosed
WO-2019149128-A1 5-CHLORO-2,4-PYRIMIDINE DERIVATIVE USED AS ANTI-TUMOR DRUG 陆柯潮 2019-08-08 WO disclosed
EP-2990405-B1 DEUTERATED DIAMINOPYRIMIDINE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS COMPRISING SUCH COMPOUNDS SUZHOU ZELGEN BIOPHARMACEUTICALS CO LTD (CN) 2019-07-17 EP disclosed
US-4818277-A HERBICIDES E. I. DU PONT DE NEMOURS AND COMPANY (US) 1989-04-04 US disclosed
EP-0306222-A2 Benzenesulfonanilide derivatives and fungicides for agriculture and horticulture HOKKO CHEMICAL INDUSTRY CO., LTD (JP) 1989-03-08 EP disclosed
EP-0035893-B1 HERBICIDAL BENZENE- AND PYRIDINE-SULFONAMIDE DERIVATIVES E.I. DU PONT DE NEMOURS AND COMPANY (US) 1985-11-21 EP disclosed
US-4303673-A N-Propionylsarcosineanilides, process for their preparation, and pharmaceutical compositions containing them A. NATTERMANN & CIE. GMBH (DE) 1981-12-01 US disclosed
EP-0035893-A2 Herbicidal benzene- and pyridine-sulfonamide derivatives E.I. DU PONT DE NEMOURS AND COMPANY (US) 1981-09-16 EP disclosed
US-4239688-A Herbicidal N-(haloacetyl)-N-(N'-methylenepyrrolidonyl-2-mercaptoalkylanilines GAF CORPORATION (US) 1980-12-16 US disclosed
US-4203901-A Process for making N-(N'-methylenepyrrolidonyl)-2-substituted anilines GAF CORPORATION (US) 1980-05-20 US disclosed
US-4202821-A N-(N'-Methylenepyrrolidonyl)-2-substituted anilines GAF CORPORATION (US) 1980-05-13 US disclosed
US-4146688-A CHAIN EXTENSION BAYER AKTIENGESELLSCHAFT (DE) 1979-03-27 US disclosed
US-3985894-A Method of controlling rice blast with N-(alkylthiophenyl)maleimides THE DOW CHEMICAL COMPANY (US) 1976-10-12 US 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 (2 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-10618884-B2 Deuterated diaminopyrimidine compounds and pharmaceutical compositions comprising such compounds DCK, DPYD, BRAF MAPT 1055/4885KMT2A 1408/4885NPSR1 4580/4885
US-20200039935-A1 Chemical Process for Preparing Pyrimidine Derivatives and Intermediates Thereof PDXK, DCK, DPYD MAPT 3373/4885KMT2A 1186/4885NPSR1 3466/4885

“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.