SCHEMBL855370

SCHEMBL855370

O=C1c2ccccc2C(=O)C1c1ccncc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 6/20 1.00
MAPT P10636 5/20 1.00
NPC1 O15118 5/20 1.00
TP53 P04637 3/20 1.00
SMN1; SMN2 Q16637 2/20 1.00
MAPK10 P53779 1/20 1.00
LMNA P02545 1/20 0.68
CYP1A2 P05177 1/20 0.68
CYP3A4 P08684 1/20 0.68
MAPK1 P28482 1/20 0.68
HTR2B P41595 1/20 0.68
KMT2A Q03164 4/20 0.59
MEN1 O00255 3/20 0.59
KDM4E B2RXH2 2/20 0.59
GAA P10253 2/20 0.59
HPGD P15428 1/20 0.58
MAOA P21397 1/20 0.58
PTGS2 P35354 1/20 0.58
ALDH1A1 P00352 2/20 0.57
CYP19A1 P11511 2/20 0.50

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
SCHEMBL6274633 0.87 RAB9A (0.76) RAB9AMAPTNPC1TP53SMN1; SMN2
SCHEMBL14768931 0.84 RAB9A (0.72) RAB9AMAPTNPC1TP53SMN1; SMN2
Phenindione SCHEMBL29388073 0.81 MAPT (1.00) RAB9AMAPTNPC1TP53SMN1; SMN2
Phenindione SCHEMBL33831 0.81 MAPT (1.00) RAB9AMAPTNPC1TP53SMN1; SMN2
SCHEMBL10559114 0.79 MAPT (0.95) RAB9AMAPTNPC1TP53SMN1; SMN2
Phenindione SCHEMBL6827577 0.79 MAPT (0.95) RAB9AMAPTNPC1TP53SMN1; SMN2
Phenindione SCHEMBL1443973 0.79 MAPT (0.95) RAB9AMAPTNPC1TP53SMN1; SMN2
SCHEMBL14940174 0.78 MAPT (0.63) RAB9AMAPTNPC1TP53SMN1; SMN2
Phenindione SCHEMBL16782144 0.77 MAPT (0.91) RAB9AMAPTNPC1TP53SMN1; SMN2
SCHEMBL6607855 0.76 MAPT (0.65) RAB9AMAPTNPC1TP53SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10768174-B2 Attachment of proteins to interfaces for use in nonlinear optical detection BLUELIGHT THERAPEUTICS, INC. (US) 2020-09-08 US disclosed
US-20200064354-A1 SYSTEMS AND METHODS FOR HIGH THROUGHPUT ANALYSIS OF CONFORMATION IN BIOLOGICAL ENTITIES QUANTA THERAPEUTICS, INC. 2020-02-27 US disclosed
US-10451630-B2 Systems and methods for high throughput analysis of conformation in biological entities Biodesy, Inc. (US) 2019-10-22 US disclosed
US-20180340940-A1 SYSTEMS AND METHODS FOR HIGH THROUGHPUT ANALYSIS OF CONFORMATION IN BIOLOGICAL ENTITIES QUANTA THERAPEUTICS, INC. 2018-11-29 US disclosed
US-20170350883-A1 ATTACHMENT OF PROTEINS TO INTERFACES FOR USE IN NONLINEAR OPTICAL DETECTION QUANTA THERAPEUTICS, INC. 2017-12-07 US disclosed
WO-2013068785-A1 INDANONE AND INDANDIONE DERIVATIVES AND HETEROCYCLIC ANALOGS ACTELION PHARMACEUTICALS LTD (CH) 2013-05-16 WO disclosed
US-8431717-B2 Process for the preparation of 5-(2-ethyl-dihydro-1H-inden-2-yl)-1H-imidazole and salts thereof JSC GRINDEKS (LV) 2013-04-30 US disclosed
EP-2225209-B1 PROCESS FOR THE PREPARATION OF 5-(2-ETHYL-DIHYDRO-1H-INDEN-2-YL)-1H-IMIDAZOLE AND SALTS THEREOF GRINDEKS JSC (LV) 2012-03-28 EP disclosed
US-20110028733-A1 PROCESS FOR THE PREPARATION OF 5-(2-ETHYL-DIHYDRO-1H-INDEN-2-YL)-1H-IMIDAZOLE AND SALTS THEREOF JSC GRINDEKS (LV) 2011-02-03 US disclosed
EP-2225209-A1 PROCESS FOR THE PREPARATION OF 5-(2-ETHYL-DIHYDRO-1H-INDEN-2-YL)-1H-IMIDAZOLE AND SALTS THEREOF Grindeks, a joint stock company (LV) 2010-09-08 EP disclosed
WO-2009071584-A1 PROCESS FOR THE PREPARATION OF 5-(2-ETHYL-DIHYDRO-1H-INDEN-2-YL)-1H-IMIDAZOLE AND SALTS THEREOF GRINDEKS, A JOINT STOCK COMPANY (LV) 2009-06-11 WO 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-20110028733-A1 PROCESS FOR THE PREPARATION OF 5-(2-ETHYL-DIHYDRO-1H-INDEN-2-YL)-1H-IMIDAZOLE AND SALTS THEREOF CYP3A5, CYP3A4, IPO5 RAB9A 2556/4885MAPT 1241/4885NPC1 396/4885

“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.