SCHEMBL265044

SCHEMBL265044

OCCc1cc(C(F)(F)F)cc(C(F)(F)F)c1

nearest known ligand 0.48

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 2/20 0.48
DAO P14920 2/20 0.44
CES2 O00748 1/20 0.43
DHODH Q02127 1/20 0.42
TACR1 P25103 8/20 0.41
TAAR1 Q96RJ0 1/20 0.39
RXRA P19793 1/20 0.39
RXRB P28702 1/20 0.39
RXRG P48443 1/20 0.39
MTOR P42345 1/20 0.39
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39

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
SCHEMBL1295021 0.87 RXRA (0.41) IDO1DAODHODHTACR1TAAR1
SCHEMBL80590 0.86 IDO1 (0.45) IDO1DAOCES2DHODHTACR1
SCHEMBL3985022 0.86 NOTUM (0.41) IDO1DAODHODHTACR1TAAR1
SCHEMBL12398665 0.86 IDO1 (0.41) IDO1DAODHODHTACR1TAAR1
SCHEMBL10316301 0.86 NOS1 (0.42) IDO1DAODHODHTACR1TAAR1
SCHEMBL24214278 0.81 MRGPRX4 (0.50) CES2DHODHTACR1RXRARXRB
SCHEMBL31736118 0.81 DAO (0.36) IDO1DAOCES2DHODHTACR1
SCHEMBL15738902 0.80 IDO1 (0.44) IDO1DAOCES2DHODHTACR1
SCHEMBL265486 0.80 IDO1 (0.52) IDO1DAOCES2TACR1RXRA
SCHEMBL156739 0.79 TAAR1 (0.67) IDO1DAODHODHTAAR1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106399398-B Biological preparation method of (R) -3, 5-bis (trifluoromethyl) phenethyl alcohol 上海医药工业研究院 2024-07-09 CN claimed
CN-117778341-A Immobilized carbonyl reductase based on protein tag self-assembly and application of immobilized carbonyl reductase in continuous catalysis preparation of aprepitant intermediate 浙江工业大学 2024-03-29 CN claimed
CN-113388627-A Reductase LX05 gene, genetic engineering bacterium containing gene and application of gene 湖南科技大学 2021-09-14 CN claimed
CN-112048538-A Method for preparing (S) - [3, 5-bis (trifluoromethyl) phenyl ] ethanol by using Verticillium terrestris 浙江工业大学 2020-12-08 CN claimed
CN-107326049-A Recombinate ketoreductase and prepare (R) -3,5- two(Trifluoromethyl)Application in benzyl carbinol 尚科生物医药(上海)有限公司 2017-11-07 CN claimed
EP-2970927-A1 IMMOBILIZED KETOREDUCTASES AND PROCESS FOR MAKING AND USING IMMOBILIZED KETOREDUCTASE Merck Sharp & Dohme Corp. (US) 2016-01-20 EP claimed
CN-103773724-B Rhodococcus XS1012 and preparing the application in chiral alcohol JIANG University OF TECHNOLOGY (CN) 2016-01-20 CN claimed
WO-2014150633-A1 IMMOBILIZED KETOREDUCTASES AND PROCESS FOR MAKING AND USING IMMOBILIZED KETOREDUCTASE MERCK SHARP & DOHME CORP. (US) 2014-09-25 WO claimed
CN-103773724-A Rhodococcus erythropolis XS1012 and application thereof in preparation of chiral alcohol UNIV ZHEJIANG TECHNOLOGY 2014-05-07 CN claimed
JP-2006521344-A 2006-09-21 JP claimed
EP-1622872-A1 1,2,4-SUBSTITUERTE 1,2,3,4-TETRAHYDRO-AND 1,2 DIHYDRO-QUINOLINE AND 1,2,3,4-TETRAHYDRO-QUINOXALINE DERIVATIVES AS CETP INHIBITORS FOR THE TREATMENT OF ATHEROSCLEROSIS AND OBESITY Pfizer Products Inc. (US) 2006-02-08 EP claimed
WO-2004094353-A1 PROCESS FOR THE MANUFACTURE OF 3,5-BIS(TRIFLUOROMETHYL)PHENYL-1-HYDROXYETHANE AND DERIVATIVE THEREOF MITENI S.P.A. (IT) 2004-11-04 WO claimed
WO-2004094358-A1 PROCESS FOR THE MANUFACTURE OF 3,5-BIS(TRIFLUOROMETHYL)ACETOPHENONE MITENI S.P.A. (IT) 2004-11-04 WO claimed
US-20040204450-A1 Quinoline and quinoxaline compounds PFIZER INC 2004-10-14 US claimed
WO-2004085401-A1 1,2,4-SUBSTITUTED 1,2,3,4-TETRAHYDRO-AND 1,2 DIHYDRO-QUINOLINE AND 1,2,3,4-TETRAHYDRO-QUINOXALINE DERIVATIVES AS CETP INHIBITORS FOR THE TREATMENT OF ATHEROSCLEROSIS AND OBESITY PFIZER PRODUCTS INC. (US) 2004-10-07 WO claimed
EP-1292583-A4 PROCESS FOR THE SYNTHESIS OF (2R, 2-ALPHA-R)-4-BENZYL-2- 1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHOXY]-1,4-OXAZIN-3-ONE MERCK & CO INC (US) 2004-02-25 EP claimed
EP-1292583-A1 PROCESS FOR THE SYNTHESIS OF (2R, 2-ALPHA-R)-4-BENZYL-2- 1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHOXY]-1,4-OXAZIN-3-ONE Merck & Co., Inc. (US) 2003-03-19 EP claimed
EP-1196364-A1 PROCESS FOR THE SYNTHESIS OF (R)-1-(3,5-BIS(TRIFLUOROMETHYL)-PHENYL)ETHAN-1-OL BY ASYMMETRIC TRANSFER HYDROGENATION Merck & Co., Inc. (US) 2002-04-17 EP claimed
WO-2001094323-A1 PROCESS FOR THE SYNTHESIS OF (2R, 2-ALPHA-R)-4-BENZYL-2-[1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHOXY]-1,4-OXAZIN-3-ONE MERCK & CO., INC. (US) 2001-12-13 WO claimed
WO-2001002326-A1 PROCESS FOR THE SYNTHESIS OF (R)-1-(3,5-BIS(TRIFLUOROMETHYL)-PHENYL)ETHAN-1-OL BY ASYMMETRIC TRANSFER HYDROGENATION MERCK & CO., INC. (US) 2001-01-11 WO 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 (1 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-20040204450-A1 Quinoline and quinoxaline compounds LDLR, APOB, PON1 IDO1 1293/4885DAO 2279/4885CES2 487/4885

“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.