Chloroform

Chloroform

SCHEMBL3364287

ClC(Cl)Cl.ClC(Cl)Cl.O=C(O)O

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GSK3AGSK3BIMPA1

The experimentally established mechanism targets of Chloroform. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.58
CA1 P00915 1/20 0.56
CA2 P00918 1/20 0.56
CA9 Q16790 1/20 0.56
ALDH1A1 P00352 4/20 0.50
TSHR P16473 3/20 0.36
TP53 P04637 2/20 0.36
THRB P10828 1/20 0.36
RECQL P46063 1/20 0.36
HPGD P15428 2/20 0.33
HSD17B10 Q99714 2/20 0.33
TDP1 Q9NUW8 2/20 0.33
ABCB11 O95342 1/20 0.33
F2 P00734 1/20 0.33
KDM4E B2RXH2 1/20 0.33
MEN1 O00255 1/20 0.33
MAPT P10636 1/20 0.33
ALOX15 P16050 1/20 0.33
KMT2A Q03164 1/20 0.33
CYP2C19 P33261 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
Chloroform SCHEMBL8829928 1.00
Chloroform SCHEMBL27532873 1.00 LMNA (0.58) LMNACA1CA2CA9ALDH1A1
Chloroform SCHEMBL2360396 0.95
Chloroform SCHEMBL3804250 0.95
Chloroform SCHEMBL27824229 0.84
Oxalic Acid SCHEMBL28297039 0.84 LMNA (0.54) LMNACA1CA2CA9ALDH1A1
Bicarbonate SCHEMBL29569190 0.82
Chloroform SCHEMBL28055651 0.82
Chloroform SCHEMBL28940869 0.80
Acetic Acid SCHEMBL694363 0.80

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112159402-B Preparation method of rivaroxaban 南京法恩化学有限公司 2022-04-05 CN claimed
CN-112159402-A Preparation method of rivaroxaban 南京法恩化学有限公司 2021-01-01 CN claimed
CN-114149401-B Synthesis method of vinyl ethylene carbonate 苏州华一新能源科技股份有限公司 2023-03-24 CN disclosed
CN-112159402-B Preparation method of rivaroxaban 南京法恩化学有限公司 2022-04-05 CN disclosed
CN-114149401-A Synthesis method of vinyl ethylene carbonate 苏州华一新能源科技股份有限公司 2022-03-08 CN disclosed
CN-107880877-B Preparation method and application of monodisperse polymer fluorescent microspheres 上海艾瑞德生物科技有限公司 2021-02-26 CN disclosed
CN-112159402-A Preparation method of rivaroxaban 南京法恩化学有限公司 2021-01-01 CN disclosed
US-7691931-B2 Organic-inorganic hybrid material and method of preparing the organic-inorganic hybrid material, and electrophotographic photoreceptor, process cartridge, image forming apparatus and image forming method using the organic-inorganic hybrid material RICOH COMPANY LTD. (JP) 2010-04-06 US disclosed
US-20060122303-A1 Organic-inorganic hybrid material and method of preparing the organic-inorganic hybrid material, and electrophotographic photoreceptor, process cartridge, image forming apparatus and image forming method using the organic-inorganic hybrid material RICOH COMPANY, LTD. (JP) 2006-06-08 US disclosed
US-6486293-B1 Electrophotographic photoconductor and method of producing aromatic polycarbonate resin for use in the photoconductor RICOH COMPANY, LTD. (JP) 2002-11-26 US disclosed
US-6187492-B1 ELECTROCONDUCTIVE SUPPORT COATED WITH A PHOTOCONDUCTIVE CHARGE TRANSPORT LAYER OF SOLUTION POLYMERIZED COPOLYCARBONATE HAVING TRIARYLAMINE DIPHENOL UNITS AND DIHYDROXY SUBSTITUTED ARYL BENZOATE UNITS; PHOTOSENSITIVITY RICOH COMPANY, LTD. (JP) 2001-02-13 US disclosed