SCHEMBL2866567

SCHEMBL2866567

CC(=O)c1cc(Cl)c(N)c(Cl)c1

nearest known ligand 0.48

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
HSD11B1 P28845 11/20 0.48
CA5A P35218 1/20 0.46
ALDH1A1 P00352 3/20 0.46
CYP3A4 P08684 1/20 0.46
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41
CA9 Q16790 1/20 0.41
LMNA P02545 1/20 0.39
PRKCI P41743 1/20 0.38
TTR P02766 1/20 0.38
KDM4E B2RXH2 1/20 0.37
GAA P10253 1/20 0.37

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
SCHEMBL10467015 0.89 PRKCI (0.43) HSD11B1CA5AALDH1A1CYP3A4LMNA
SCHEMBL3854731 0.87 CA5A (0.40) HSD11B1CA5AALDH1A1CYP3A4LMNA
SCHEMBL8431166 0.86 CA1 (0.47) HSD11B1CA5AALDH1A1CYP3A4CA1
SCHEMBL5166345 0.81 NPFFR2 (0.44) HSD11B1
SCHEMBL31749059 0.81 NPFFR2 (0.44) HSD11B1
SCHEMBL8934245 0.81 HSD11B1 (0.36) HSD11B1CA5AALDH1A1KDM4EGAA
SCHEMBL5981527 0.80 HSD11B1 (0.52) HSD11B1ALDH1A1CYP3A4CA1CA2
SCHEMBL7779178 0.80 CA5A (0.50) CA5AALDH1A1CYP3A4LMNATTR
SCHEMBL3002757 0.78 HSD11B1 (0.50) HSD11B1ALDH1A1CYP3A4CA1CA2
SCHEMBL3243039 0.78 TTR (0.62) CA5AALDH1A1CYP3A4LMNATTR

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
CN-108929276-B Method for preparing pyrimidine compounds from methyl ketone compounds and nitrile compounds 湖南大学 2021-08-31 CN claimed
CN-109096126-B Deuterium labeled D9Synthesis method of clenbuterol hydrochloride 东莞暨南大学研究院 2021-03-26 CN claimed
CN-105968021-A Stable isotope labeling Clenproperol compound and synthesis method thereof 上海化工研究院 2016-09-28 CN claimed
US-20240051916-A1 METHOD FOR PRODUCING N-(HETERO)ARYL (METH)ACRYLAMIDE COMPOUND FUJIFILM CORPORATION (JP) 2024-02-15 US disclosed
CN-117398332-A Keli boron Luo Ruangao 杭州中美华东制药有限公司 2024-01-16 CN disclosed
CN-117242052-A Method for producing N- (hetero) aryl (meth) acrylamide compound 富士胶片株式会社 2023-12-15 CN disclosed
WO-2022249994-A1 METHOD FOR PRODUCING N-(HETERO)ARYL(METH)ACRYLAMIDE COMPOUNDS 富士フイルム株式会社 2022-12-01 WO disclosed
CN-109912434-B Synthesis method of phenylethanolamine beta receptor agonist 上海安谱实验科技股份有限公司 2022-07-12 CN disclosed
CN-108929276-B Method for preparing pyrimidine compounds from methyl ketone compounds and nitrile compounds 湖南大学 2021-08-31 CN disclosed
CN-113061096-A Preparation method of stable isotope labeled krusel 阿尔塔(天津)标准物质研究院有限公司 2021-07-02 CN disclosed
CN-109096126-B Deuterium labeled D9Synthesis method of clenbuterol hydrochloride 东莞暨南大学研究院 2021-03-26 CN disclosed
US-4323575-A TOPICAL ANTIINFLAMMATORY AGENTS IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1982-04-06 US disclosed
US-4237048-A COLORFASTNESS; FOR DYEING NATURAL AND SYNTHETIC FIBERS BAYER AKTIENGESELLSCHAFT (DE) 1980-12-02 US disclosed
EP-0019411-A1 1-Phenyl-2-aminoethanol derivatives, processes for their manufacture and pharmaceutical compositions thereof IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1980-11-26 EP disclosed
US-4145363-A ANTIASTHMATICS YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1979-03-20 US disclosed
EP-0000809-A1 Anti-inflammatory 1-phenylethanolamine derivatives, pharmaceutical compositions thereof and processes for their manufacture IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1979-02-21 EP disclosed
US-4105655-A PHENYL-AZO-ANILINO DYESTUFF BAYER AKTIENGESELLSCHAFT (DE) 1978-08-08 US disclosed
US-4083844-A Phenylazo orthocyano phenylazo or orthocyano phenylazo phenylazo containing dyestuffs BAYER AKTIENGESELLSCHAFT (DT) 1978-04-11 US disclosed
US-4063025-A PROPHYLAXIS, ANTIASTHMATIC YAMANOUCHI PHARMACEUTICAL CO., LTD. (JA) 1977-12-13 US disclosed
US-3962209-A PROCESS FOR PREPARING AZO DYESTUFFS WITH ORTHO-AZO CYANO GROUPS BY CYANO EXCHANGE OF METAL CYANIDES AND HALO DYESTUFFS BAYER AKTIENGESELLSCHAFT (DT) 1976-06-08 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 (1 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-20240051916-A1 METHOD FOR PRODUCING N-(HETERO)ARYL (METH)ACRYLAMIDE COMPOUND NAT1, AHR, PAM HSD11B1 473/4885CA5A 3814/4885ALDH1A1 784/4885

“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.