SCHEMBL147622

SCHEMBL147622

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
SCHEMBL145000 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL5043328 1.00 KDM4E (0.56) KDM4EADRA2AADRA2CLMNAHIF1A
SCHEMBL2065907 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 200 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113330004-B Differential solubility driven asymmetric conversion process for substituted 2H-chromene-3-carboxylic acids 株式会社AskAt 2023-11-17 CN claimed
EP-3906232-B1 PROCESS FOR THE DIFFERENTIAL SOLUBILITY-DRIVEN ASYMMETRIC TRANSFORMATION OF SUBSTITUTED 2H-CHROMENE-3-CARBOXYLIC ACIDS ASKAT INC (JP) 2023-05-10 EP 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
US-11065238-B2 Inhibitors of gangliosides metabolism for the treatment of motor neuron diseases ICM (INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE) (FR) 2021-07-20 US 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-9833768-B2 Affinity reagents for protein purification IMPOSSIBLE FOODS INC. (US) 2017-12-05 US claimed
US-20170320041-A1 AFFINITY REAGENTS FOR PROTEIN PURIFICATION IMPOSSIBLE FOODS INC. 2017-11-09 US claimed
US-9737875-B2 Affinity reagents for protein purification IMPOSSIBLE FOODS INC. (US) 2017-08-22 US 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
US-20110039324-A1 COMPOSITIONS AND METHODS FOR ENHANCING APOPTOSIS GENENTECH, INC. (US) 2011-02-17 US claimed
US-20090148921-A1 Compositions and methods for enhancing apoptosis GENENTECH, INC. (US) 2009-06-11 US claimed
EP-1590666-B1 COMPOSITIONS AND METHODS FOR ENHANCING APOPTOSIS GENENTECH INC (US) 2008-07-09 EP claimed
US-20050020834-A1 Method for preparation of sulphostin and its analogue or intermediates thereof NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2005-01-27 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-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

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-20050020834-A1 Method for preparation of sulphostin and its analogue or intermediates thereof SOST, PTMS, FGF23 KDM4E 3668/4885ADRA2A 4343/4885ADRA2C 4227/4885
US-11065238-B2 Inhibitors of gangliosides metabolism for the treatment of motor neuron diseases GBA1, SMN1; SMN2, GAA KDM4E 3898/4885ADRA2A 4123/4885ADRA2C 4133/4885
US-20170320041-A1 AFFINITY REAGENTS FOR PROTEIN PURIFICATION RAB5IF, MRPL21, RPS27A KDM4E 3795/4885ADRA2A 4513/4885ADRA2C 4433/4885

“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.