SCHEMBL710

SCHEMBL710

CCCCc1nc(Cl)c(C=O)[nH]1

nearest known ligand 0.41

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.40
MAPK1 P28482 1/20 0.40
PARP1 P09874 1/20 0.39
GPR84 Q9NQS5 5/20 0.37
GSK3B P49841 1/20 0.36
TYMP P19971 1/20 0.34
HIF1A Q16665 1/20 0.33

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
SCHEMBL895 0.89 GLA (0.37) TYMP
SCHEMBL2762904 0.87 ALDH1A1 (0.35) ALDH1A1MAPK1PARP1GPR84GSK3B
SCHEMBL14169365 0.87 ALDH1A1 (0.38) ALDH1A1MAPK1PARP1GPR84GSK3B
SCHEMBL3027900 0.82 GAA (0.38)
SCHEMBL3735333 0.81 PARP1 (0.43) ALDH1A1MAPK1PARP1GPR84GSK3B
SCHEMBL17949542 0.81 ALDH1A1 (0.41) ALDH1A1MAPK1PARP1GPR84GSK3B
SCHEMBL14003653 0.80 ALDH1A1 (0.36) ALDH1A1MAPK1PARP1GPR84GSK3B
SCHEMBL8438737 0.79 ALDH1A1 (0.40) ALDH1A1MAPK1PARP1GPR84GSK3B
SCHEMBL1257638 0.79 ALDH1A1 (0.40) ALDH1A1MAPK1PARP1GPR84GSK3B
SCHEMBL2454194 0.76 PARP1 (0.42) ALDH1A1MAPK1PARP1GPR84GSK3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117276497-A Asphalt-based coated resin-based hard carbon composite material and preparation method and application thereof 常州烯源谷新材料科技有限公司 2023-12-22 CN claimed
CN-116735742-A High performance liquid chromatography detection method for imidazole aldehyde and related substances thereof 云南云天化股份有限公司 2023-09-12 CN claimed
CN-114605393-B Method for preparing losartan by micro-channel continuous flow 浙江工业大学 2023-06-27 CN claimed
US-11668708-B2 Method for reducing measurement error in latex agglutination immunoassay SEKISUI MEDICAL CO., LTD. (JP) 2023-06-06 US claimed
CN-114605393-A Method for preparing losartan by micro-channel continuous flow 浙江工业大学 2022-06-10 CN claimed
CN-112225702-A Preparation method of 2-n-butyl-4-chloro-5-formylimidazole 浙江花蝶染料化工有限公司 2021-01-15 CN claimed
CN-111592495-A Preparation method of 2-n-butyl-4-chloro-5-formylimidazole 上海启讯医药科技有限公司 2020-08-28 CN claimed
CN-111087388-A Hydrazone group bridged naphthalimide imidazole compound and preparation method and application thereof 西南大学 2020-05-01 CN claimed
CN-106995411-A A kind of preparation method of the formyl imidazoles of 2 normal-butyl, 4 chlorine 5 滨海三甬药业化学有限公司 2017-08-01 CN claimed
CN-101838242-B Method for synthesizing 2-normal-butyl-4-chloro-5-formylimidazole UNIV ZHEJIANG TECHNOLOGY 2015-07-15 CN claimed
EP-1871745-A2 PREPARATION OF 2-SUBSTITUTED 4-CHLORO-5-FORMYLIMIDAZOLES BY VILSMEIER REACTION OF THE CONDENSATION PRODUCT OF GLYCINE AND AN IMIDO ESTER WITH A FORMAMIDE IN THE PRESENCE OF A TRIFLATE (TRIFLUORMETHANESULPHONATE) CATALYST Disham Pharmaceuticals and Chemicals Ltd. (IN) 2008-01-02 EP claimed
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I CADILA PHARMACEUTICALS LTD. (IN) 2007-10-25 US claimed
WO-2007119246-A2 AN IMPROVED PROCESS FOR THE MANUFACTURE OF LOSARTAN POTASSIUM UNICHEM LABORATORIES LIMITED (IN) 2007-10-25 WO claimed
WO-2007020654-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF LOSARTAN SUVEN LIFE SCIENCES (IN) 2007-02-22 WO claimed
WO-2006110037-A2 PREPARATION OF 2-SUBSTITUTED 4-CHL0R0-5-F0RMYLIMIDAZ0LES BY VILSMEIER REACTION OF THE CONDENSATION PRODUCT OF GLYCINE AND AN IMIDO ESTER WITH A FORMAMIDE IN THE PRESENCE OF A TRIFLATE (TRIFLUORMETHANΞSULPHONATE) CATALYST DISHMAN PHARMACEUTICALS AND CHEMICALS LTD. (IN) 2006-10-19 WO claimed
US-7041832-B2 Processes for preparing losartan and losartan potassium TAVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2006-05-09 US claimed
WO-2006038223-A1 A PROCESS FOR PREPARATION OF 2-N-BUTYL -4-CHLORO - 1 - {[2`- (2-TRIPHENYLMETHYL - 2H - TETRAZOLE - 5- YL) - 1, 1’ - BIPHENYL-4-YL] METHYL}-LH- IMIDAZOIE-5-METHANOL (INTERMEDIATE OF LOSARTAN) MATRIX LABORATORIES LTD (IN) 2006-04-13 WO claimed
EP-1474417-B1 PROCESSES FOR PREPARING LOSARTAN AND LOSARTAN POTASSIUM TEVA PHARMA (IL) 2006-03-22 EP claimed
US-20040034077-A1 Processes for preparing losartan and losartan an potassium TEVA PHARMACEUTICALS INDUSTRIES, LTD. (IL) 2004-02-19 US claimed
CN-1369492-A Non-peptide angiotonin II receptor antagon Jw sartan compounds and its synthesizing process and application WANG JIANWU (CN) 2002-09-18 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 (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-20070249839-A1 Process for the Preparation of Losartan Potassium Form I AGTR1, REN, AGT ALDH1A1 802/4885MAPK1 1106/4885PARP1 3577/4885
US-20040034077-A1 Processes for preparing losartan and losartan an potassium REN, ACE, AGT ALDH1A1 248/4885MAPK1 856/4885PARP1 1858/4885

“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.