SCHEMBL5682194

SCHEMBL5682194

CC1(C)COP(=O)(O)O[C@H]1c1ccc(Cl)cc1Cl

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.39
MAPT P10636 2/20 0.39
THRB P10828 1/20 0.39
HTT P42858 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39
USP2 O75604 1/20 0.39
KMT2A Q03164 2/20 0.36
KDM4E B2RXH2 2/20 0.36
LMNA P02545 1/20 0.36
MAPK1 P28482 1/20 0.36
DPP4 P27487 1/20 0.34
GAA P10253 3/20 0.34
TSHR P16473 1/20 0.34
AGTR1 P30556 1/20 0.34
HTR2A P28223 1/20 0.34
HTR2C P28335 1/20 0.34
HTR2B P41595 1/20 0.34
MEN1 O00255 1/20 0.34
CYP2C9 P11712 1/20 0.34
CYP2C19 P33261 1/20 0.34

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
SCHEMBL4069903 1.00 ALDH1A1 (0.39) ALDH1A1MAPTTHRBHTTNPSR1
SCHEMBL5678330 1.00 ALDH1A1 (0.39) ALDH1A1MAPTTHRBHTTNPSR1
SCHEMBL7565959 0.86 MAPT (0.41) ALDH1A1MAPTTHRBHTTNPSR1
SCHEMBL2026167 0.84 PTGS2 (0.37) ALDH1A1KMT2AKDM4EGAATSHR
SCHEMBL5680629 0.82 MAPT (0.38) ALDH1A1MAPTTHRBHTTNPSR1
SCHEMBL17485156 0.82 SLC9A1 (0.36) HTTTP53
SCHEMBL547467 0.82 HTR2A (0.35) ALDH1A1MAPTNPSR1KMT2AKDM4E
SCHEMBL5682299 0.81 MAPK1 (0.41) ALDH1A1MAPTHTTNPSR1KMT2A
SCHEMBL28194083 0.80 HTR5A (0.31) HTR2AHTR2C
SCHEMBL28194084 0.80 HTR5A (0.31) HTR2AHTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107602464-B Method for preparing biaryl quinoline antibiotics by optical resolution 宜昌人福药业有限责任公司 2020-02-18 CN claimed
CN-107602464-B Method for preparing biaryl quinoline antibiotics by optical resolution 宜昌人福药业有限责任公司 2020-02-18 CN disclosed
EP-1227085-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE NAPHTHALENE DERIVATIVE AND OPTICAL RESOLVER THEREFOR TAKEDA PHARMACEUTICAL (JP) 2006-03-15 EP disclosed
US-6800778-B1 OPTICALLY ACTIVE CYCLIC PHOSPHORUS COMPOUND USED AS REAGENT FOR OPTICAL RESOLUTION TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2004-10-05 US disclosed
EP-1227085-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE NAPHTHALENE DERIVATIVE AND OPTICAL RESOLVER THEREFOR Takeda Chemical Industries, Ltd. (JP) 2002-07-31 EP disclosed