SCHEMBL2380939

SCHEMBL2380939

C[C@@H](O)CCCO

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
SCHEMBL50388 1.00
SCHEMBL54852 1.00
1,4-Butanediol SCHEMBL8983355 0.97 TDP1 (0.44)
SCHEMBL27787445 0.97
SCHEMBL28299896 0.97
1,5-Pentanediol SCHEMBL6905317 0.94 ALDH1A1 (0.43)
1,6-Hexanediol SCHEMBL7211787 0.94 ALDH1A1 (0.43)
SCHEMBL17686274 0.91 TDP1 (0.40)
SCHEMBL41064 0.90
SCHEMBL3401418 0.90

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115490708-B Sulfonamide macrocyclic derivative, preparation method and application thereof 苏州亚盛药业有限公司 2025-01-24 CN disclosed
CN-115490708-A Sulfonamide macrocyclic derivatives, and preparation method and application thereof 苏州亚盛药业有限公司 2022-12-20 CN disclosed
US-8450354-B2 Substituted imidazo[1,2-b]pyridazine derivatives, pharmaceutical compositions, and methods of use as β-secretase inhibitors HIGH POINT PHARMACEUTICALS, LLC (US) 2013-05-28 US disclosed
EP-2549874-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE AS BETA-SECRETASE INHIBITORS High Point Pharmaceuticals, LLC (US) 2013-01-30 EP disclosed
US-20110237570-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE AS BETA-SECRETASE INHIBITORS HIGH POINT PHARMACEUTICALS, LLC (US) 2011-09-29 US disclosed
US-7807426-B2 Processes for producing optically active 1-substituted 2-methylpyrrolidine KANEKA CORPORATION (JP) 2010-10-05 US disclosed
EP-1735324-B1 PREPARATION OF P-CHIROGENIC PHOSPHOLANES AND THEIR USE IN ASYMETRIC SYNTHESIS WARNER LAMBERT CO (US) 2008-08-20 EP disclosed
US-7390931-B2 Preparation of P-chirogenic phospholanes and their use in asymmetric synthesis PFIZER INC. (US) 2008-06-24 US disclosed
US-20070292926-A1 Processes for Producing Optically Active 1-Substituted 2-Methylpyrrolidine and Intermediate Therefor KANEKA CORPORATION (JP) 2007-12-20 US disclosed
US-20070149781-A1 Process for preparing bisphospholane ligands DEGUSSA AG (DE) 2007-06-28 US disclosed
EP-1735324-A1 PREPARATION OF P-CHIROGENIC PHOSPHOLANES AND THEIR USE IN ASYMETRIC SYNTHESIS Warner-Lambert Company LLC (US) 2006-12-27 EP disclosed
EP-1715054-A1 PROCESSES FOR PRODUCING OPTICALLY ACTIVE 1-SUBSTITUTED 2-METHYLPYRROLIDINE AND INTERMEDIATE THEREFOR KANEKA CORPORATION (JP) 2006-10-25 EP disclosed
WO-2005095424-A1 PREPARATION OF P-CHIROGENIC PHOSPHOLANES AND THEIR USE IN ASYMETRIC SYNTHESIS WARNER-LAMBERT COMPANY LLC (US) 2005-10-13 WO disclosed
US-20050222464-A1 Preparation of P-chirogenic phospholanes and their use in asymmetric synthesis HOGE GARRETT S II 2005-10-06 US disclosed
US-6103517-A ECONOMICAL, SIMPLE PRODUCTION OF SECONDARY ALCOHOL CONTAINING ASSYMETRIC CARBON HAVING SUBSTITUTED METHYL GROUP AND HAVING ALKOXY AS TERMINAL GROUP BY ASSYMETRIC TRANSESTERIFICATION USING VINYL PROPIONATE AND LIPASE FROM CANDIDA ANTARCIA MITSUBISHI GAS CHEMICAL COMPANY (JP) 2000-08-15 US disclosed