SCHEMBL2637828

SCHEMBL2637828

O=C(c1ccc(F)cc1)c1cc(Br)ccc1Cl

nearest known ligand 0.50

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.50
MAPT P10636 8/20 0.48
POLB P06746 2/20 0.46
TP53 P04637 1/20 0.46
HPGD P15428 3/20 0.44
LMNA P02545 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
NPSR1 Q6W5P4 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
CYP1A2 P05177 2/20 0.42
GAA P10253 1/20 0.42
RECQL P46063 1/20 0.42
CYP2C9 P11712 1/20 0.42
ALOX15 P16050 1/20 0.42
CASP1 P29466 1/20 0.42
CYP2C19 P33261 1/20 0.42
AKR1C3 P42330 1/20 0.41

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
SCHEMBL29740498 1.00 ALDH1A1 (0.50) ALDH1A1MAPTPOLBTP53HPGD
SCHEMBL17755 0.85 ALDH1A1 (0.51) ALDH1A1MAPTPOLBHPGDLMNA
SCHEMBL30482609 0.85 ALDH1A1 (0.51) ALDH1A1MAPTPOLBHPGDLMNA
SCHEMBL1457582 0.83 ALDH1A1 (0.50) ALDH1A1MAPTPOLBTP53HPGD
SCHEMBL499767 0.83 MAPT (0.67) ALDH1A1MAPTPOLBHPGDLMNA
SCHEMBL610759 0.83 ALDH1A1 (0.53) ALDH1A1MAPTTP53LMNARECQL
SCHEMBL27751160 0.83 MAPT (0.67) ALDH1A1MAPTPOLBHPGDLMNA
SCHEMBL17193968 0.81 CYP1A2 (0.67) ALDH1A1MAPTPOLBHPGDLMNA
SCHEMBL30494732 0.81 CYP1A2 (0.67) ALDH1A1MAPTPOLBHPGDLMNA
SCHEMBL499583 0.81 ALDH1A1 (0.47) ALDH1A1MAPTPOLBHPGDLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118619823-A Preparation method of 4-bromo-1-chloro-2- (4- (2-cyclopropyloxy ethoxy) benzyl) benzene 杭州科巢生物科技有限公司 2024-09-10 CN claimed
CN-118546055-A Preparation method of (1R, 3S, 5S) -3- (4- (5-bromo-2-chlorobenzyl) phenoxy) bicyclo [3.1.0] hexane 山东科巢生物制药有限公司 2024-08-27 CN claimed
CN-118388436-A Preparation method of englitz intermediate and englitz impurity 江苏阿尔法药业股份有限公司 2024-07-26 CN claimed
CN-116262691-A (5-bromo-2-chlorophenyl) (4-fluorophenyl) methanone 苏州小栗医药科技有限公司 2023-06-16 CN claimed
EP-1881990-B1 PROCESSES FOR PREPARING OF GLUCOPYRANOSYL-SUBSTITUTED BENZYL-BENZENE DERIVATIVES AND INTERMEDIATES THEREIN BOEHRINGER INGELHEIM INT (DE) 2016-02-17 EP claimed
US-9127034-B2 Processes for preparing of glucopyranosyl-substituted benzyl-benzene derivates and intermediates therein BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2015-09-08 US claimed
JP-4834080-B2 2011-12-07 JP claimed
US-20100240879-A1 PROCESSES FOR PREPARING OF GLUCOPYRANOSYL-SUBSTITUTED BENZYL-BENZENE DERIVATES AND INTERMEDIATES THEREIN BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2010-09-23 US claimed
CN-101193903-A Process for preparing glucopyranosyl-substituted benzylbenzene derivatives and intermediates thereof BOEHRINGER INGELHEIM INT (DE) 2008-06-04 CN claimed
EP-1881990-A1 PROCESSES FOR PREPARING OF GLUCOPYRANOSYL-SUBSTITUTED BENZYL-BENZENE DERIVATIVES AND INTERMEDIATES THEREIN Boehringer Ingelheim International GmbH (DE) 2008-01-30 EP claimed
WO-2006120208-A1 PROCESSES FOR PREPARING OF GLUCOPYRANOSYL-SUBSTITUTED BENZYL-BENZENE DERIVATIVES AND INTERMEDIATES THEREIN BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2006-11-16 WO claimed
US-20060258749-A1 Processes for preparing of glucopyranosyl-substituted benzyl-benzene derivatives and intermediates therein BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2006-11-16 US claimed
WO-2025056984-A1 A NOVEL PROCESS FOR THE PREPARATION OF BEXAGLIFLOZIN A SGLT2 INHIBITOR AND ITS INTERMEDIATES THEREOF VIJAYASRI ORGANICS PRIVATE LIMITED (IN) 2025-03-20 WO disclosed
CN-118619823-A Preparation method of 4-bromo-1-chloro-2- (4- (2-cyclopropyloxy ethoxy) benzyl) benzene 杭州科巢生物科技有限公司 2024-09-10 CN disclosed
CN-118546055-A Preparation method of (1R, 3S, 5S) -3- (4- (5-bromo-2-chlorobenzyl) phenoxy) bicyclo [3.1.0] hexane 山东科巢生物制药有限公司 2024-08-27 CN disclosed
CN-118388436-A Preparation method of englitz intermediate and englitz impurity 江苏阿尔法药业股份有限公司 2024-07-26 CN disclosed
CN-101193903-A Process for preparing glucopyranosyl-substituted benzylbenzene derivatives and intermediates thereof BOEHRINGER INGELHEIM INT (DE) 2008-06-04 CN disclosed
EP-1881990-A1 PROCESSES FOR PREPARING OF GLUCOPYRANOSYL-SUBSTITUTED BENZYL-BENZENE DERIVATIVES AND INTERMEDIATES THEREIN Boehringer Ingelheim International GmbH (DE) 2008-01-30 EP disclosed
WO-2006120208-A1 PROCESSES FOR PREPARING OF GLUCOPYRANOSYL-SUBSTITUTED BENZYL-BENZENE DERIVATIVES AND INTERMEDIATES THEREIN BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2006-11-16 WO disclosed
US-20060258749-A1 Processes for preparing of glucopyranosyl-substituted benzyl-benzene derivatives and intermediates therein BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2006-11-16 US disclosed

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

For each of this compound's patents that has machine-readable text (2 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-20060258749-A1 Processes for preparing of glucopyranosyl-substituted benzyl-benzene derivatives and intermediates therein UGGT1, B3GAT3, B4GALT1 ALDH1A1 273/4885MAPT 4699/4885POLB 1080/4885
US-20100240879-A1 PROCESSES FOR PREPARING OF GLUCOPYRANOSYL-SUBSTITUTED BENZYL-BENZENE DERIVATES AND INTERMEDIATES THEREIN UGGT1, B3GAT3, B4GALT1 ALDH1A1 200/4885MAPT 4669/4885POLB 1337/4885

“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.