SCHEMBL2833792

SCHEMBL2833792

NCc1c(N)cccc1Cl

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 4/20 0.54
TSHR P16473 2/20 0.50
DPP4 P27487 2/20 0.50
PNMT P11086 3/20 0.48
NR4A2 P43354 1/20 0.48
ALDH1A1 P00352 1/20 0.48
CYP3A4 P08684 2/20 0.40
PIK3CA P42336 1/20 0.40
AKR1B1 P15121 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.39
MEN1 O00255 1/20 0.37
LMNA P02545 1/20 0.37
HTR1A P08908 1/20 0.37
ADRA2A P08913 1/20 0.37
CYP2D6 P10635 1/20 0.37
CYP2C9 P11712 1/20 0.37
ADRA2B P18089 1/20 0.37
ADRA2C P18825 1/20 0.37
MAOA P21397 1/20 0.37
ADRA1D P25100 1/20 0.37

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
SCHEMBL30528615 1.00 TAAR1 (0.54) TAAR1TSHRDPP4PNMTNR4A2
SCHEMBL110460 0.85 TAAR1 (0.64) TAAR1TSHRDPP4PNMTCYP3A4
SCHEMBL11758388 0.83 TSHR (0.52) TAAR1TSHRDPP4PNMTNR4A2
Hydrochloric Acid SCHEMBL7895201 0.82 TAAR1 (0.61) TAAR1TSHRDPP4PNMTCYP3A4
Hydrochloric Acid SCHEMBL460781 0.79 CYP3A4 (0.43) TAAR1TSHRDPP4PNMTALDH1A1
SCHEMBL1372359 0.79 TSHR (0.48) TAAR1TSHRDPP4PNMTNR4A2
SCHEMBL2911470 0.79 TSHR (0.48) TAAR1TSHRDPP4PNMTNR4A2
SCHEMBL3791097 0.79 ALDH1A1 (0.52) TAAR1TSHRDPP4PNMTNR4A2
SCHEMBL11571234 0.79 TSHR (0.48) TAAR1TSHRDPP4PNMTNR4A2
SCHEMBL29701394 0.79 ALDH1A1 (0.52) TAAR1TSHRDPP4PNMTNR4A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101203244-A Compositions of rennin inhibitor and insulin secernent or insulin sensitizer NOVARTIS AG (CH) 2008-06-18 CN claimed
CN-101163504-A Combination therapy XENON PHARMACEUTICALS INC (CA) 2008-04-16 CN claimed
CN-115925642-B Synthesis method of 1, 4-benzodiazepine Zhuo Zahuan derivative 枣庄学院 2025-02-07 CN disclosed
US-20240018125-A1 CYCLIC ISOTHIOUREA DERIVATIVES AS CXCR4 MODULATORS ERMIUM THERAPEUTICS (FR) 2024-01-18 US disclosed
EP-4217353-A1 CYCLIC ISOTHIOUREA DERIVATIVES AS CXCR4 MODULATORS Ermium Therapeutics (FR) 2023-08-02 EP disclosed
CN-115925642-A Synthesis method of 1, 4-benzodiazepine heterocyclic derivative 枣庄学院 2023-04-07 CN disclosed
WO-2022064075-A1 CYCLIC ISOTHIOUREA DERIVATIVES AS CXCR4 MODULATORS ERMIUM THERAPEUTICS (FR) 2022-03-31 WO disclosed
CN-111925334-B Synthetic method of 5H-1, 4-benzodiazepine compound 扬州大学 2021-11-23 CN disclosed
CN-111925334-A Synthetic method of 5H-1, 4-benzodiazepine compound 扬州大学 2020-11-13 CN disclosed
US-9174984-B2 Chemical compounds GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2015-11-03 US disclosed
US-9174984-B2 Chemical compounds GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2015-11-03 US disclosed
US-20060252779-A1 (3,4-Dihydro-quinazolin-2-yl)-(2-aryloxy-ethyl)-amine HOFFMANN-LA ROCHE INC. 2006-11-09 US disclosed
WO-2006108773-A1 (3,4-DIHYDRO-QUINAZOLIN-2-YL)-INDAN-1-YL-AMINES F. HOFFMANN-LA ROCHE AG (CH) 2006-10-19 WO disclosed
US-20060229323-A1 (3,4-Dihydro-quinazolin-2-yl)-indan-1-yl-amines F. HOFFMANN-LA ROCHE AG (CH) 2006-10-12 US disclosed
US-20060211716-A1 (3,4-Dihydro-quinazolin-2-yl)-aryl-amines F. HOFFMAN-LA ROCHE AG, A SWISS COMPANY (CH) 2006-09-21 US disclosed
WO-2006097391-A1 USE OF 2 -ANILINO - 3 , 4 -DIHYDRO - QUINAZOLINES AS 5HT5A RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2006-09-21 WO disclosed
US-20060035909-A1 2,6,9-trisubstituted 8-azapurines such as 2-(4-aminocyclohexylamino)-6-benzylamino-9-isopropyl-8-azapurine, used as cyclin-dependent kinase inhibitors, in the treatment of skin disorders, viral infections, cancer, arthritis, lupus, diabetes, multiple sclerosis, restenosis, polycystic kidney disease, gout UNIVERZITA PALACKEHO V OLOMOUCI (CZ) 2006-02-16 US disclosed
US-20050080097-A1 Pyrazolo[4,3-D]pyrimidines, processes for their preparation and methods for therapy USTAV EXPERIMENTALNI BOTANIKY AV CR (INSTITUTE OF EXPERIMENTAL BOTANY ACADEMY OF 2005-04-14 US disclosed
US-20050043328-A1 Heterocyclic compound based on n6-substituted adenine, methods, of their preparation, their use for preparation of drugs, cosmetic preparations and growth regulators, pharmaceutical preparations, cosmetic preparations and growth regulators containing these compounds USTAV EPERIMENTALNI BOTANIKY AKADEMI VED CESKE REPUBILIKY (CZ) 2005-02-24 US disclosed
EP-1348707-A1 Pyrazolo[4,3-d]pyrimidines, processes for their preparation and methods for therapy Ustav Experimentalni Botaniky AV CR (Institute of Experimental Botany Academy of Sciences of the Czech Republic) (CZ) 2003-10-01 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 (7 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-20060211716-A1 (3,4-Dihydro-quinazolin-2-yl)-aryl-amines HTR5A, HTR1A, HTR2C TAAR1 74/4885TSHR 317/4885DPP4 1008/4885
US-20060229323-A1 (3,4-Dihydro-quinazolin-2-yl)-indan-1-yl-amines HTR5A, HTR1A, HTR1E TAAR1 71/4885TSHR 108/4885DPP4 2648/4885
US-20050080097-A1 Pyrazolo[4,3-D]pyrimidines, processes for their preparation and methods for therapy CBR3, DHFR, AKR1C3 TAAR1 705/4885TSHR 51/4885DPP4 3429/4885
US-20050043328-A1 Heterocyclic compound based on n6-substituted adenine, methods, of their preparation, their use for preparation of drugs, cosmetic preparations and growth regulators, pharmaceutical preparations, cosmetic preparations and growth regulators containing these compounds ATIC, UMPS, CCNB1 TAAR1 3350/4885TSHR 1625/4885DPP4 4483/4885
US-20060252779-A1 (3,4-Dihydro-quinazolin-2-yl)-(2-aryloxy-ethyl)-amine HTR5A, NPY5R, HTR3A TAAR1 50/4885TSHR 148/4885DPP4 1321/4885
US-20240018125-A1 CYCLIC ISOTHIOUREA DERIVATIVES AS CXCR4 MODULATORS CXCR4, CXCR1, CXCL12 TAAR1 2787/4885TSHR 1575/4885DPP4 3718/4885
US-20060035909-A1 2,6,9-trisubstituted 8-azapurines such as 2-(4-aminocyclohexylamino)-6-benzylamino-9-isopropyl-8-azapurine, used as cyclin-dependent kinase inhibitors, in the treatment of skin disorders, viral infections, cancer, arthritis, lupus, diabetes, multiple sclerosis, restenosis, polycystic kidney disease, gout CDK8, CDK6, CDK1 TAAR1 1013/4885TSHR 2431/4885DPP4 1706/4885

“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.