SCHEMBL838442

SCHEMBL838442

COc1ccc(Br)c(C)c1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.54
NPC1 O15118 1/20 0.54
RAB9A P51151 1/20 0.54
HAO1 Q9UJM8 1/20 0.51
MEN1 O00255 3/20 0.49
KMT2A Q03164 3/20 0.49
SMN1; SMN2 Q16637 1/20 0.47
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA2 P00918 2/20 0.46
CA7 P43166 2/20 0.46
CA9 Q16790 2/20 0.46
CA14 Q9ULX7 2/20 0.46
GAA P10253 1/20 0.44
ACHE P22303 2/20 0.44
CYP1A2 P05177 1/20 0.43
CYP2A6 P11509 1/20 0.43
TP53 P04637 1/20 0.42
HTR3E A5X5Y0 1/20 0.42
HTR3B O95264 1/20 0.42

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
SCHEMBL30294336 1.00 MAPT (0.54) MAPTNPC1RAB9AHAO1MEN1
SCHEMBL1257369 0.98 MAPT (0.53) MAPTNPC1RAB9AHAO1MEN1
SCHEMBL3527439 0.83 CA12 (0.48) MAPTNPC1RAB9AMEN1KMT2A
SCHEMBL29427042 0.83 CA12 (0.48) MAPTNPC1RAB9AMEN1KMT2A
SCHEMBL13614304 0.83 MAPT (0.53) MAPTNPC1RAB9AMEN1KMT2A
SCHEMBL1134723 0.82 CA1 (0.53) MAPTNPC1RAB9AMEN1KMT2A
SCHEMBL30250475 0.82 CA1 (0.53) MAPTNPC1RAB9AMEN1KMT2A
SCHEMBL7465577 0.78 LTA4H (0.53) MAPTNPC1RAB9AMEN1KMT2A
SCHEMBL6449465 0.78 CA1 (0.48) MAPTNPC1RAB9AMEN1KMT2A
SCHEMBL25405284 0.77 SMN1; SMN2 (0.53) MAPTNPC1RAB9AHAO1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114736102-B Synthesis method of 4-bromo-3-methylanisole 山东默锐科技有限公司 2024-03-12 CN claimed
CN-116178182-B Preparation method of 2-methyl-4-methoxy diphenylamine 山东默锐科技有限公司 2023-09-19 CN claimed
CN-108794307-B Micro-reaction system and method for synthesizing 4-bromo-3-methylanisole by solvent method 山东道可化学有限公司 2022-11-11 CN claimed
CN-114736102-A Synthesis method of 4-bromo-3-methylanisole 山东默锐科技有限公司 2022-07-12 CN claimed
CN-109053391-B Micro-reaction system and method for synthesizing 4-bromo-3-methylanisole by two-phase method 山东道可化学有限公司 2022-06-28 CN claimed
CN-108996524-B Method for preparing bromide salt from bromine-containing waste 寿光富康制药有限公司 2021-05-11 CN claimed
CN-111892529-A 6-chloro-5-hydroxyisoindole-1-one and synthesis method thereof 南通大学 2020-11-06 CN claimed
CN-108218676-B Method for synthesizing 4-bromo-3-methylanisole 清华大学 2020-08-18 CN claimed
US-20150344486-A1 PYRIMIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS CYCLACEL LIMITED (GB) 2015-12-03 US claimed
CN-102718692-B Preparation method of 7-bit methyl-5-bit oxygen-substituted indole compounds SUZHOU HEJIAN MEDICAL TECHNOLOGY CO LTD 2014-01-08 CN claimed
CN-101786956-B Method for deacylating N-acylated diphenylamine or ring-substituted derivatives thereof MORIS CHEMICAL CO LTD 2011-02-16 CN claimed
CN-101786956-A Method for deacylating N-acylated diphenylamine or ring-substituted derivatives thereof MORIS CHEMICAL CO LTD 2010-07-28 CN claimed
EP-2183239-A1 SULFONAMIDES AS TRPM8 MODULATORS Janssen Pharmaceutica, N.V. (BE) 2010-05-12 EP claimed
US-20090264474-A1 SULFONAMIDES AS TRPM8 MODULATORS JANSSEN PHARMACEUTICA, N.V. (BE) 2009-10-22 US claimed
WO-2009012430-A1 SULFONAMIDES AS TRPM8 MODULATORS JANSSEN PHARMACEUTICA N.V. (BE) 2009-01-22 WO claimed
EP-1055658-B1 Process for cis-1- 2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]ethyl pyrrolidine PFIZER PROD INC (US) 2003-03-12 EP claimed
US-20020042524-A1 Process for cis-1{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy] ethyl}pyrrolidine CHIU CHARLES K F (US) 2002-04-11 US claimed
US-6323345-B1 BROMINATING 2-BROMO-5-METHOXY-TOLUENE TO PROVIDE 1-BROMO-2-BROMOMETHYL-4-METHOXYBENZENE; DECARBOXYLATION, REACTING WITH ETHYLENE GLYCOL; REACTING WITH N-BUTYL LITHIUM AND 4-BENZYLOXY BENZONITRILE; HYDROLYSIS, HYDROGENATION PFIZER INC. 2001-11-27 US claimed
EP-1055658-A2 Process for cis-1- 2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]ethyl pyrrolidine Pfizer Products Inc. (US) 2000-11-29 EP claimed
US-5008464-A Anisole bromination EAST SHORT CHEMICAL COMPANY (US) 1991-04-16 US 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-20020042524-A1 Process for cis-1{2-[4-(6-methoxy-2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy] ethyl}pyrrolidine P4HA1, PAH, DNM1 MAPT 1877/4885NPC1 815/4885RAB9A 1513/4885
US-20150344486-A1 PYRIMIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS DCK, DTYMK, TK1 MAPT 2501/4885NPC1 2831/4885RAB9A 2853/4885
US-20090264474-A1 SULFONAMIDES AS TRPM8 MODULATORS TRPM8, TRPM5, TRPM2 MAPT 3324/4885NPC1 1670/4885RAB9A 818/4885

“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.