SCHEMBL1471041

SCHEMBL1471041

C[C@@H]1CN(Cc2ccccc2)CCN1

nearest known ligand 0.58

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
SIGMAR1 Q99720 2/20 0.58
ACHE P22303 2/20 0.54
LTA4H P09960 1/20 0.53
CYP1A2 P05177 1/20 0.49
CYP3A4 P08684 1/20 0.49
CYP2D6 P10635 1/20 0.49
CYP2C19 P33261 1/20 0.49
ALDH1A1 P00352 1/20 0.49
MC4R P32245 1/20 0.49
MLNR O43193 3/20 0.47
LMNA P02545 1/20 0.47
POLB P06746 1/20 0.47
BCHE P06276 1/20 0.46
BACE1 P56817 1/20 0.46
XIAP P98170 1/20 0.46
BIRC2 Q13490 1/20 0.46
FUCA1 P04066 2/20 0.46

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
SCHEMBL1307820 1.00 SIGMAR1 (0.58) SIGMAR1ACHELTA4HCYP1A2CYP3A4
SCHEMBL1826258 1.00 SIGMAR1 (0.58) SIGMAR1ACHELTA4HCYP1A2CYP3A4
Hydrochloric Acid SCHEMBL18788467 0.98 SIGMAR1 (0.56) SIGMAR1ACHELTA4HCYP1A2CYP3A4
Dimethylamine SCHEMBL6787869 0.95 LTA4H (0.53) SIGMAR1ACHELTA4HCYP1A2CYP3A4
SCHEMBL12469761 0.90 CYP2D6 (0.54) SIGMAR1ACHELTA4HCYP1A2CYP3A4
SCHEMBL17763473 0.85 ACHE (0.67) SIGMAR1ACHEALDH1A1MC4RLMNA
SCHEMBL17830169 0.85 ACHE (0.67) SIGMAR1ACHEALDH1A1MC4RLMNA
SCHEMBL13330940 0.85 CXCR4 (0.53) ACHECYP3A4ALDH1A1MLNRLMNA
SCHEMBL3158803 0.85 MLNR (0.49) SIGMAR1CYP3A4ALDH1A1MLNRXIAP
SCHEMBL17495605 0.85 ACHE (0.67) SIGMAR1ACHEALDH1A1MC4RLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240067625-A1 SMALL-MOLECULE MODULATORS OF THE ORPHAN NUCLEAR RECEPTOR TLX BAYLOR COLLEGE OF MEDICINE (US) 2024-02-29 US disclosed
WO-2022140643-A1 SMALL-MOLECULE MODULATORS OF THE ORPHAN NUCLEAR RECEPTOR TLX BAYLOR COLLEGE OF MEDICINE (US) 2022-06-30 WO disclosed
EP-1805158-B1 SULFONYL-SUBSTITUTED BICYCLIC COMPOUNDS AS MODULATORS OF PPAR KALYPSYS INC (US) 2018-06-27 EP disclosed
US-20170174703-A1 QUINOLINE DERIVATIVES AS SMO INHIBITORS GUANGDONG ZHONGSHENG PHARMACEUTICAL CO., LTD (CN) 2017-06-22 US disclosed
EP-2566859-B1 PICOLINAMIDE AND PYRIMIDINE-4-CARBOXAMIDE COMPOUNDS, PROCESS FOR PREPARING AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME SK CHEMICALS CO LTD (KR) 2016-12-21 EP disclosed
US-9096571-B2 Picolinamide and pyrimidine-4-carboxamide compounds, process for preparing and pharmaceutical composition comprising the same SK CHEMICALS CO., LTD. (KR) 2015-08-04 US disclosed
CN-103025721-B Picolinamide and pyrimidine-4-carboxamide compounds, process for preparing and pharmaceutical composition comprising the same SK CHEMICALS CO LTD 2015-06-17 CN disclosed
US-20130210811-A1 PICOLINAMIDE AND PYRIMIDINE-4-CARBOXAMIDE COMPOUNDS, PROCESS FOR PREPARING AND PHAMACEUTICAL COMPOSITION COMPRISING THE SAME SK CHEMICALS CO., LTD. (KR) 2013-08-15 US disclosed
CN-103025721-A Picolinamide and pyrimidine-4-carboxamide compounds, process for preparing and pharmaceutical composition comprising the same SK CHEMICALS CO LTD 2013-04-03 CN disclosed
US-8404708-B2 Dual NK1/NK3 receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2013-03-26 US disclosed
EP-1368340-B1 PIPERAZINE DERIVATIVES AS MELANOCORTIN RECEPTOR AGONISTS LILLY CO ELI (US) 2005-08-10 EP disclosed
WO-2005056015-A1 SUBSTITUTED PIPERAZINES CHEMOCENTRYX, INC. (US) 2005-06-23 WO disclosed
CN-1629146-A Process for synthesis of chiral 2-substituted piperazine and its derivatives SHANGHAI INST MATERIA MEDICA (CN) 2005-06-22 CN disclosed
US-20050090533-A1 Dual NK1/NK3 receptor antagonists F. HOFMANN-LA ROCHE AG (CH) 2005-04-28 US disclosed
WO-2005002577-A1 DUAL NK1/NK3 ANTAGONISTS FOR TREATING SCHIZOPHRENIA F. HOFFMANN-LA ROCHE AG (CH) 2005-01-13 WO disclosed
US-20040162282-A1 Substituted piperazines CHEMOCENTRYX, INC. 2004-08-19 US disclosed
US-20040092507-A1 Melanocortin receptor agonists ELI LILLY AND COMPANY 2004-05-13 US disclosed
EP-1368340-A1 PIPERAZINE DERIVATIVES AS MELANOCORTIN RECEPTOR AGONISTS ELI LILLY AND COMPANY (US) 2003-12-10 EP disclosed
EP-1204654-B1 BENZOFURYLPIPERAZINES: 5-HT2C SEROTONIN RECEPTOR AGONISTS LILLY CO ELI (US) 2003-07-23 EP disclosed
WO-2002059108-A1 MELANOCORTIN RECEPTOR AGONISTS ELI LILLY AND COMPANY (US) 2002-08-01 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 (6 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-20040092507-A1 Melanocortin receptor agonists MC1R, MC4R, MC5R SIGMAR1 318/4885ACHE 3483/4885LTA4H 1589/4885
US-20050090533-A1 Dual NK1/NK3 receptor antagonists TACR2, TAC3, TACR1 SIGMAR1 336/4885ACHE 3263/4885LTA4H 1010/4885
US-20240067625-A1 SMALL-MOLECULE MODULATORS OF THE ORPHAN NUCLEAR RECEPTOR TLX NR2E1, NR2E3, NR4A2 SIGMAR1 812/4885ACHE 2535/4885LTA4H 823/4885
US-20130210811-A1 PICOLINAMIDE AND PYRIMIDINE-4-CARBOXAMIDE COMPOUNDS, PROCESS FOR PREPARING AND PHAMACEUTICAL COMPOSITION COMPRISING THE SAME HSD11B1, HSD11B2, G6PC1 SIGMAR1 3966/4885ACHE 3723/4885LTA4H 256/4885
US-20170174703-A1 QUINOLINE DERIVATIVES AS SMO INHIBITORS SMO, GLI1, SHH SIGMAR1 3478/4885ACHE 2659/4885LTA4H 4017/4885
US-20040162282-A1 Substituted piperazines CCR1, CCR3, CCRL2 SIGMAR1 342/4885ACHE 4869/4885LTA4H 279/4885

“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.