SCHEMBL8240347

SCHEMBL8240347

CCCN(Cc1ccccc1)Cc1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
HRH3 Q9Y5N1 1/20 0.61
RORC P51449 4/20 0.58
CNR2 P34972 1/20 0.53
BCHE P06276 4/20 0.53
TSHR P16473 3/20 0.52
ALDH1A1 P00352 1/20 0.52
HSD17B10 Q99714 1/20 0.50
DRD2 P14416 1/20 0.49
OPRM1 P35372 1/20 0.49
DRD3 P35462 1/20 0.49
OPRD1 P41143 1/20 0.49
OPRK1 P41145 1/20 0.49
KDM4E B2RXH2 1/20 0.48
AOC3 Q16853 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
Hydrochloric Acid SCHEMBL3183297 0.98 HRH3 (0.59) HRH3RORCCNR2BCHETSHR
SCHEMBL330083 0.95 HRH3 (0.68) HRH3RORCCNR2BCHETSHR
Hydrochloric Acid SCHEMBL17710415 0.93 HRH3 (0.65) HRH3RORCCNR2BCHETSHR
Water SCHEMBL28117059 0.93 HRH3 (0.65) HRH3RORCCNR2BCHETSHR
SCHEMBL20145799 0.91 HRH3 (0.57) HRH3RORCCNR2BCHETSHR
SCHEMBL9286253 0.91 HRH3 (0.57) HRH3RORCCNR2BCHETSHR
Hydrochloric Acid SCHEMBL11571118 0.89 HRH3 (0.55) HRH3RORCCNR2BCHETSHR
SCHEMBL3156308 0.88 MAPT (0.62) HRH3RORCCNR2BCHEAOC3
SCHEMBL9485158 0.87 MAPT (0.61) HRH3RORCBCHETSHRHSD17B10
SCHEMBL3372139 0.87 HRH3 (0.53) HRH3RORCCNR2BCHETSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10472565-B2 Low temperature activator systems and methods for chemiluminescent reactions CYALUME TECHNOLOGIES, INC. (US) 2019-11-12 US claimed
EP-3004286-B1 BROAD TEMPERATURE PERFORMANCE CHEMILUMINESCENT SYSTEMS AND METHODS CYALUME TECH INC (US) 2019-08-28 EP claimed
EP-3004286-A1 BROAD TEMPERATURE PERFORMANCE CHEMILUMINESCENT SYSTEMS AND METHODS Cyalume Technologies, Inc (US) 2016-04-13 EP claimed
US-9115305-B2 Broad temperature performance chemiluminescent systems and methods CYALUME TECHNOLOGIES, INC. (US) 2015-08-25 US claimed
US-20140356975-A1 LOW TEMPERATURE ACTIVATOR SYSTEMS AND METHODS FOR CHEMILUMINESCENT REACTIONS Cyalume Technologies (US) 2014-12-04 US claimed
WO-2014194332-A1 BROAD TEMPERATURE PERFORMANCE CHEMILUMINESCENT SYSTEMS AND METHODS Cyalume Technologies (US) 2014-12-04 WO claimed
US-20140353559-A1 BROAD TEMPERATURE PERFORMANCE CHEMILUMINESCENT SYSTEMS AND METHODS Cyalume Technologies (US) 2014-12-04 US claimed
WO-2024026338-A1 N-HETEROCYLIC GPCR RECEPTOR AGONISTS, PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME, AND METHODS FOR THEIR USE CARMOT THERAPEUTICS, INC. (US) 2024-02-01 WO disclosed
EP-3872064-B1 FLUORINATED IMIDE SALT COMPOUND AND SURFACTANT MITSUBISHI MAT ELECTRONIC CHEMICALS CO LTD (JP) 2023-09-20 EP disclosed
US-20230079107-A1 COMPOSITIONS AND METHODS FOR THE TREATMENT OF HUMAN IMMUNODEFICIENCY VIRUS CIDARA THERAPEUTICS, INC. 2023-03-16 US disclosed
CN-108778997-B Method for the rapid calcination of zeolitic materials 巴斯夫欧洲公司 2023-01-17 CN disclosed
CN-112996772-B Fluorine-containing imide salt compound and surfactant 三菱材料电子化成株式会社 2022-10-28 CN disclosed
US-11414381-B2 Fluorinated imide salt compound and surfactant MITSUBISHI MATERIALS ELECTRONIC CHEMICALS CO., LTD. (JP) 2022-08-16 US disclosed
US-4234723-A COMPLEXES WITH HYDROXYBENZOATE ANIONS AND AMINE LIGANDS, PHOTOSTABILITY CIBA-GEIGY CORPORATION (US) 1980-11-18 US disclosed
US-4231921-A COMPLEX OF A METAL WITH PIPERIDINE WITH ONE ENOLATE GROUP, POLYMERS CIBA-GEIGY CORPORATION (US) 1980-11-04 US disclosed
US-4186267-A LIGHT STABILIZERS FOR POLYOLEFINS CIBA-GEIGY CORPORATION (US) 1980-01-29 US disclosed
EP-0000700-A1 Metal complexes with a chelating anion comprising a phenolate group, their preparation and their use as light stabilizers, especially for polymeric substances CIBA-GEIGY AG (CH) 1979-02-21 EP disclosed
EP-0000487-A1 Compounds containing enol groups, metal chelates made therefrom, their preparation and use as light stabilizers, especially for polymeric substances. CIBA-GEIGY AG (CH) 1979-02-07 EP disclosed
US-4046788-A ORTHO- OR PARA-HYDROXYBENZOATE ANIONS, AMINE LIGAND CIBA-GEIGY CORPORATION (US) 1977-09-06 US disclosed
US-3948852-A Nickel stabilisers for synthetic polymers CIBA-GEIGY CORPORATION (US) 1976-04-06 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-11414381-B2 Fluorinated imide salt compound and surfactant NHERF1, AFF1, SCN1A HRH3 2766/4885RORC 3724/4885CNR2 4187/4885
US-20230079107-A1 COMPOSITIONS AND METHODS FOR THE TREATMENT OF HUMAN IMMUNODEFICIENCY VIRUS FCGR3B, FCGR1A, FCGR2A HRH3 1600/4885RORC 3919/4885CNR2 2783/4885

“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.