SCHEMBL1834561

SCHEMBL1834561

OCC1CC1c1ccccc1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2C P28335 11/20 0.63
MAOB P27338 10/20 0.63
HTR2B P41595 6/20 0.63
HTR2A P28223 4/20 0.63
MAOA P21397 7/20 0.48
KDM1A O60341 5/20 0.48
CYP2C19 P33261 4/20 0.48
CYP2B6 P20813 3/20 0.48
CYP1A2 P05177 2/20 0.48
CYP2D6 P10635 2/20 0.48
CYP2C9 P11712 2/20 0.48
LMNA P02545 2/20 0.48
TAAR1 Q96RJ0 2/20 0.48
CYP3A4 P08684 1/20 0.48
HTR1A P08908 1/20 0.48
ADRA2A P08913 1/20 0.48
CYP2A6 P11509 1/20 0.48
SLC6A2 P23975 1/20 0.48
ADRA1A P35348 1/20 0.48
DRD3 P35462 1/20 0.48

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
SCHEMBL16761697 1.00 HTR2C (0.63) HTR2CMAOBHTR2BHTR2AMAOA
SCHEMBL9043644 1.00 HTR2C (0.63) HTR2CMAOBHTR2BHTR2AMAOA
SCHEMBL7492289 1.00 HTR2C (0.63) HTR2CMAOBHTR2BHTR2AMAOA
SCHEMBL21480339 0.88 KDM1A (0.55) HTR2CMAOBHTR2BHTR2AKDM1A
SCHEMBL20208695 0.88 KDM1A (0.55) HTR2CMAOBHTR2BHTR2AKDM1A
SCHEMBL25262357 0.83 HTR2C (0.59) HTR2CMAOBHTR2BHTR2AMAOA
SCHEMBL17080568 0.78 HTR2C (0.41) HTR2CMAOBHTR2BHTR2ASLC6A2
SCHEMBL19262111 0.78 HTR2C (0.63) HTR2CHTR2BHTR2ASLC6A2SLC6A3
SCHEMBL16585035 0.78 HTR2C (0.66) HTR2CHTR2BHTR2AKDM1ASLC6A2
SCHEMBL2826042 0.78 HTR2C (0.66) HTR2CMAOBHTR2BHTR2AKDM1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014009767-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF 1-ARYL 2-AMINOMETHYL CYCLOPROPANE CARBOXYAMIDE (Z) DERIVATIVES, THEIR ISOMERS AND SALTS MICRO LABS LIMITED (IN) 2014-01-16 WO claimed
WO-2023069720-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF MONTE ROSA THERAPEUTICS, INC. (US) 2023-04-27 WO disclosed
EP-3102198-B1 ANTIDIABETIC COMPOUNDS MERCK SHARP & DOHME (US) 2020-08-26 EP disclosed
US-10059667-B2 Antidiabetic compounds MERCK SHARP & DOHME CORP. (US) 2018-08-28 US disclosed
EP-2881384-B1 PARTIALLY SATURATED NITROGEN-CONTAINING HETEROCYCLIC COMPOUND TAISHO PHARMACEUTICAL CO LTD (JP) 2018-05-30 EP disclosed
US-9822124-B2 Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors INCYTE CORPORATION (US) 2017-11-21 US disclosed
US-9822124-B2 Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors INCYTE CORPORATION (US) 2017-11-21 US disclosed
US-9822124-B2 Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors INCYTE CORPORATION (US) 2017-11-21 US disclosed
US-9617256-B2 Antibacterial agents ACHAOGEN, INC. (US) 2017-04-11 US disclosed
US-9617256-B2 Antibacterial agents ACHAOGEN, INC. (US) 2017-04-11 US disclosed
US-5089639-A N-CYCLOALKYLALKYLAMINES, PROCESS FOR THEIR PREPARATION, THEIR USE AS A MEDICAMENT AND THEIR SYNTHESIS INTERMEDIATES JOUVEINAL S.A. (FR) 1992-02-18 US disclosed
EP-0446097-A1 Substituted etylamines, process for their preparation, their use as therapeutic agents and intermediates for their synthesis JOUVEINAL S.A. (FR) 1991-09-11 EP disclosed
EP-0445013-A1 C-cycloalkyl-alkylamines, process for their preparation, their use as therapeutic agents and intermediates for their synthesis JOUVEINAL S.A. (FR) 1991-09-04 EP disclosed
EP-0444964-A1 Milbemycin ether derivatives, their preparation and their anthelmintic uses Sankyo Company Limited (JP) 1991-09-04 EP disclosed
US-5034419-A Psychological disorders or gastrointestinal disorders L'OREAL (FR) 1991-07-23 US disclosed
US-5017723-A Psychotropic Agents JOUVEINAL S.A. (FR) 1991-05-21 US disclosed
US-5010198-A Intermediates for the synthesis of benzoxazol- and benzothiazolamine derivatives, useful as anti-anoxic agents JANSSEN PHARMACEUTICA N.V. (BE) 1991-04-23 US disclosed
EP-0184257-B1 BENZOXAZOL- AND BENZOTHIAZOLAMINE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1990-07-25 EP disclosed
US-4861785-A Benzoxazol-and benzothiazolamine derivatives, useful as anti-anoxic agents JANSSEN PHARMACEUTICA N.V. (BE) 1989-08-29 US disclosed
EP-0184257-A1 Benzoxazol- and benzothiazolamine derivatives JANSSEN PHARMACEUTICA N.V. (BE) 1986-06-11 EP 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 (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-10059667-B2 Antidiabetic compounds GPR119, GLP1R, GIPR HTR2C 986/4885MAOB 4173/4885HTR2B 901/4885

“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.