SCHEMBL2492904

SCHEMBL2492904

CCCCCN=CN

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL4255843 1.00
SCHEMBL13302530 1.00
SCHEMBL14437434 0.97
SCHEMBL10431397 0.97 MEN1 (0.46)
SCHEMBL2660180 0.97
SCHEMBL22926500 0.97 MEN1 (0.46)
SCHEMBL4476204 0.92
SCHEMBL17887834 0.79
SCHEMBL10737278 0.79
SCHEMBL6263872 0.77 TSHR (0.41)

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113288899-B Application of heterocyclic thiol compound in preparation of antitumor drugs 浙江工业大学 2022-10-11 CN disclosed
CN-113288899-A Application of heterocyclic thiol compound in preparation of antitumor drugs 浙江工业大学 2021-08-24 CN disclosed
US-9273333-B2 Process for the preparation of intermediates of HMG-CoA reductase inhibitors MYLAN LABORATORIES LTD (IN) 2016-03-01 US disclosed
WO-2014195965-A2 AN IMPROVED PROCESS FOR THE PREPARATION OF HMG-COA REDUCTASE INHIBITOR INTERMEDIATES MYLAN LABORATORIES LTD (IN) 2014-12-11 WO disclosed
US-20140349350-A1 Novel Process for the Preparation of Intermediates of HMG-CoA Reductase Inhibitors TIANISH LABORATORIES PRIVATE LIMITED (IN) 2014-11-27 US disclosed
EP-2785851-A2 PROCESS FOR PRODUCING CHIRAL STATIN SIDE CHAIN INTERMEDIATES EMPLOYING CANDIDA ANTARCTICA LIPASE B Mylan Laboratories, Limited (IN) 2014-10-08 EP disclosed
WO-2013080219-A2 NOVEL PROCESS FOR THE PREPARATION OF INTERMEDIATES OF HMG-CoA REDUCTASE INHIBITORS MYLAN LABORATORIES LTD (IN) 2013-06-06 WO disclosed
EP-2550257-A1 PHARMACEUTICALLY ACTIVE DISUBSTITUTED TRIAZINE DERIVATIVES Lead Discovery Center GmbH (DE) 2013-01-30 EP disclosed
WO-2011116951-A1 PHARMACEUTICALLY ACTIVE DISUBSTITUTED TRIAZINE DERIVATIVES LEAD DISCOVERY CENTER GMBH (DE) 2011-09-29 WO disclosed
US-7482481-B2 Method for producing isocyanates BASF AKTIENGESELLSCHAFT (DE) 2009-01-27 US disclosed
US-7211689-B2 Method for production of isocyanates BASF AKTIENGESELLSCHAFT (DE) 2007-05-01 US disclosed
US-7064233-B2 Method for producing isocyanates BASF AKTIENGESELLSCHAFT (DE) 2006-06-20 US disclosed
US-20040267047-A1 Method for production of isocyanates BASF AKTIENGESELLSCHAFT (DE) 2004-12-30 US disclosed
US-20040260117-A1 Method for producing isocyanates BASF AKTIENGESELLSCHAFT (DE) 2004-12-23 US disclosed
US-20040249193-A1 Method for producing isocyanates BASF AKTIENGESELLSCHAFT (DE) 2004-12-09 US disclosed
US-4207334-A Acylformamidine insecticidal and miticidal compounds STAUFFER CHEMICAL COMPANY (US) 1980-06-10 US disclosed
US-4130662-A Acylformanidine insecticidal and miticidal compounds STAUFFER CHEMICAL COMPANY (US) 1978-12-19 US disclosed
US-4056570-A Acylformanidine insecticidal and miticidal compounds STAUFFER CHEMICAL COMPANY (US) 1977-11-01 US disclosed
US-3962305-A INSECTICIDES, MITICIDES STAUFFER CHEMICAL COMPANY (US) 1976-06-08 US disclosed
US-3857836-A HERBICIDAL AGENTS HOECHST AG 1974-12-31 US disclosed