SCHEMBL2884020

SCHEMBL2884020

c1cc(C2CC2)ccc1C1CC1

nearest known ligand 0.57

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ESR2 Q92731 15/20 0.57
POLB P06746 1/20 0.55
ESR1 P03372 6/20 0.50
CYP3A4 P08684 2/20 0.50
CYP2C9 P11712 2/20 0.50
SLC18A3 Q16572 1/20 0.46
SIGMAR1 Q99720 1/20 0.46
NPC1 O15118 1/20 0.44
RAB9A P51151 1/20 0.44
CYP2D6 P10635 1/20 0.43
HTR2C P28335 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
SCHEMBL5147779 0.89 ESR2 (0.54) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL24961822 0.89 NPC1 (0.56) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL900534 0.84 SLC18A3 (0.50) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL3453587 0.84 ESR2 (0.46) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL11196166 0.84 ESR2 (0.77) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL1986271 0.84 ESR2 (0.81) ESR2ESR1CYP3A4CYP2C9CYP2D6
SCHEMBL5284 0.84 SLC18A3 (0.50) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL2051518 0.84 ESR2 (0.46) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL21556845 0.84 ESR2 (0.46) ESR2POLBESR1CYP3A4CYP2C9
SCHEMBL15260520 0.82 HDAC8 (0.52) ESR2SLC18A3RAB9A

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260007684-A1 AMIDE DERIVATIVES FOR INHIBITING NLRP3 AND USES THEREOF VENTUS THERAPEUTICS U S INC (US) 2026-01-08 US disclosed
EP-1858837-B1 PROCESS FOR THE PRODUCTION OF 2-(2-AMINOPHENYL)-BICYCLOPROPANE DERIVATIVES SYNGENTA PARTICIPATIONS AG (CH) 2012-05-16 EP disclosed
US-7803827-B2 1-N-amino-2-imidazolidinones and derivatives thereof which are effective as Kv1.5 potassium channel inhibitors providing atrial-selective antiarrhythmic agents; 1-(aminosulfonylamino)-3-[2-(4-methoxyphenyl)ethyl]-4-(3,4-dimethylphenyl)-2-imidazolidinone WYETH LLC (US) 2010-09-28 US disclosed
US-7514584-B2 Process for the production of 2(2-aminophenyl)-bicylopropane derivatives SYNGENTA CROP PROTECTION, INC. (US) 2009-04-07 US disclosed
US-7504517-B2 Kv1.5 potassium channel inhibitors WYETH (US) 2009-03-17 US disclosed
US-20090069342-A1 KV1.5 POTASSIUM CHANNEL INHIBITORS WYETH (US) 2009-03-12 US disclosed
US-20080161610-A1 Process For the Production of 2(2-Aminophenyl)-Bicylopropane Derivatives SYNGENTA CROP PROTECTION, INC. (US) 2008-07-03 US disclosed
US-20070299072-A1 KV1.5 POTASSIUM CHANNEL INHIBITORS WYETH (US) 2007-12-27 US disclosed
US-20070299120-A1 KV1.5 POTASSIUM CHANNEL INHIBITORS WYETH (US) 2007-12-27 US disclosed
EP-1858837-A1 PROCESS FOR THE PRODUCTION OF 2-(2-AMINOPHENYL)-BICYCLOPROPANE DERIVATIVES Syngeta Participations AG (CH) 2007-11-28 EP disclosed
WO-2006087223-A1 PROCESS FOR THE PRODUCTION OF 2- (2-AMINOPHENYL)-BICYCLOPROPANE DERIVATIVES SYNGENTA PARTICIPATIONS AG (CH) 2006-08-24 WO disclosed
WO-2006087222-A1 PROCESS FOR THE PRODUCTION OF NITROBENZOLES SYNGENTA PARTICIPATIONS AG (CH) 2006-08-24 WO disclosed
WO-2006087221-A1 PROCESS FOR THE PRODUCTION OF NITROBENZOLES SYNGENTA PARTICIPATIONS AG (CH) 2006-08-24 WO disclosed
EP-1101756-B1 Aminopyrrolidine derivatives, processes for their preparation and pharmaceutical compositions comprising them SERVIER LAB (FR) 2003-03-19 EP disclosed
US-6300366-B1 FOR THERAPY OF CARDIOVASCULAR DISEASES, ESPECIALLY ARTERIAL HYPERTENSION, ARRHYTHMIA ADIR ET COMPAGNIE (FR) 2001-10-09 US disclosed
EP-1101756-A1 Aminopyrrolidine derivatives, processes for their preparation and pharmaceutical compositions comprising them ADIR ET COMPAGNIE (FR) 2001-05-23 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 (5 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-20070299120-A1 KV1.5 POTASSIUM CHANNEL INHIBITORS KCNJ2, KCNK5, KCNH2 ESR2 4484/4885POLB 4818/4885ESR1 4782/4885
US-20070299072-A1 KV1.5 POTASSIUM CHANNEL INHIBITORS KCNA5, KCNH1, KCNK5 ESR2 4173/4885POLB 4267/4885ESR1 4782/4885
US-20090069342-A1 KV1.5 POTASSIUM CHANNEL INHIBITORS KCNJ2, KCNK5, KCNH2 ESR2 4484/4885POLB 4818/4885ESR1 4782/4885
US-20080161610-A1 Process For the Production of 2(2-Aminophenyl)-Bicylopropane Derivatives CYP1B1, CYP4B1, MAOB ESR2 3052/4885POLB 287/4885ESR1 4668/4885
US-20260007684-A1 AMIDE DERIVATIVES FOR INHIBITING NLRP3 AND USES THEREOF NOD1, NLRP3, NOD2 ESR2 1609/4885POLB 3869/4885ESR1 3360/4885

“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.