SCHEMBL145000

SCHEMBL145000

N[C@@H](CO)[C@@H](O)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.56
ADRA2A P08913 1/20 0.56
ADRA2C P18825 1/20 0.56
LMNA P02545 1/20 0.56
HIF1A Q16665 1/20 0.56
ALDH1A1 P00352 2/20 0.54
SLC6A2 P23975 1/20 0.50
SLC6A4 P31645 1/20 0.50
SLC6A3 Q01959 1/20 0.50
AOC3 Q16853 4/20 0.48
DPP4 P27487 2/20 0.44
F2 P00734 1/20 0.44

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
SCHEMBL15916220 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL605463 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL1162359 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL5043328 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL2065907 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL147622 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL3363663 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
Bromide SCHEMBL9771320 0.98 KDM4E (0.54) KDM4EADRA2AADRA2CLMNAHIF1A
Hydrochloric Acid SCHEMBL9779186 0.98 ALDH1A1 (0.57) KDM4EADRA2AADRA2CLMNAHIF1A
Benzoic Acid SCHEMBL6048463 0.87 DAO (0.48) KDM4EADRA2AADRA2CLMNAHIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025133248-A1 DIASTEREOMERIC AMINOALCOHOL AND AMINOETHER SALTS OF 2-[(4R,S)-8-FLUORO-2-[4-(3-METHOXYPHENYL)PIPERAZIN-1-YL]-3-[2-METHOXY-5-(TRIFLUOROMETHYL)PHENYL]-3,4-DIHYDROQUINAZOLIN-4-YL]ACETIC ACID AND THEIR USE FOR ENANTIOMERIC SEPARATION AIC246 AG & CO. KG (DE) 2025-06-26 WO claimed
EP-3906232-A1 PROCESS FOR THE DIFFERENTIAL SOLUBILITY-DRIVEN ASYMMETRIC TRANSFORMATION OF SUBSTITUTED 2H-CHROMENE-3-CARBOXYLIC ACIDS AskAt Inc. (JP) 2021-11-10 EP claimed
CN-113330004-A Differential solubility driven asymmetric transformation process for substituted 2H-chromene-3-carboxylic acids 株式会社AskAt 2021-08-31 CN claimed
WO-2020153279-A1 PROCESS FOR THE DIFFERENTIAL SOLUBILITY-DRIVEN ASYMMETRIC TRANSFORMATION OF SUBSTITUTED 2H-CHROMENE-3-CARBOXYLIC ACIDS ASKAT INC. (JP) 2020-07-30 WO claimed
US-20130143824-A1 COMPOSITIONS AND METHODS FOR ENHANCING APOPTOSIS GENENTECH, INC. (US) 2013-06-06 US claimed
US-20120058953-A1 COMPOSITIONS AND METHODS FOR ENHANCING APOPTOSIS GENENTECH, INC. (US) 2012-03-08 US claimed
EP-1861363-B1 METHOD OF PREPARATION OF PURE 4-PYRROLIDINOPHENYLBENZYL ETHER DERIVATIVES AS MAOB INHIBITORS HOFFMANN LA ROCHE (CH) 2011-09-28 EP claimed
US-20110039324-A1 COMPOSITIONS AND METHODS FOR ENHANCING APOPTOSIS GENENTECH, INC. (US) 2011-02-17 US claimed
EP-1397335-B1 RESOLUTION PROCESS FOR (R)-(-)-2-HYDROXY-2-(2-CHLOROPHENYL)ACETIC ACID SANOFI AVENTIS (FR) 2010-11-10 EP claimed
US-20090148921-A1 Compositions and methods for enhancing apoptosis GENENTECH, INC. (US) 2009-06-11 US claimed
US-20040242921-A1 Resolution process for (r)-(-)-2-hydroxy-2-(2-chlorophenyl) acetic acid SANOFI (FR) 2004-12-02 US claimed
EP-1457494-A1 PROCESSES FOR PREPARATION OF SULPHOSTIN AND ITS ANALOGUES OR INTERMEDIATES THEREOF Nippon Kayaku Kabushiki Kaisha (JP) 2004-09-15 EP claimed
US-20040171554-A1 Compositions and methods for enhancing apoptosis GENENTECH, INC. 2004-09-02 US claimed
EP-0783366-B1 CHROMATOGRAPHIC RESINS AND METHODS FOR USING SAME UNIV MASSEY (NZ) 2004-08-18 EP claimed
EP-1017358-B1 REDUCTION OF HAIR GROWTH GILLETTE CO (US) 2004-08-11 EP claimed
US-5939458-A APPLYING AN INHIBITOR OF AMINOACYL-TRNA SYNTHETASE TO THE SKIN GILLETTE COMPANY, THE 1999-08-17 US claimed
EP-0398288-B1 Process for preparing optically active 2-arylalkanoic acids, in particular 2-arylpropionic acids PUETTER MEDICE CHEM PHARM (DE) 1995-10-18 EP claimed
US-5380927-A Process for preparing optically active 2-aryl-alkanoic acids, in particular 2-aryl-propionic acids MEDICE CHEM.-PHARM. FABRIK PUTTER GMBH & CO. KG (DE) 1995-01-10 US claimed
EP-0398288-A2 Process for preparing optically active 2-arylalkanoic acids, in particular 2-arylpropionic acids MEDICEChem.-Pharm. Fabrik Pütter GmbH & Co. KG (DE) 1990-11-22 EP claimed
EP-0101570-B1 METHOD FOR THE RESOLUTION OF RACEMIC 2-CP-DIFLUOROMETHOXY PHENYL)-3-METHYLBUTYRIC ACID AMERICAN CYANAMID COMPANY (US) 1988-01-27 EP 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-20040242921-A1 Resolution process for (r)-(-)-2-hydroxy-2-(2-chlorophenyl) acetic acid GRHPR, HCAR2, HCAR1 KDM4E 3915/4885ADRA2A 197/4885ADRA2C 212/4885

“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.