SCHEMBL73941

SCHEMBL73941

C1CC(N2CCOCC2)CC[N]1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.44
L3MBTL3 Q96JM7 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
KDM1A O60341 1/20 0.38
MAOB P27338 1/20 0.38
OPRL1 P41146 2/20 0.38
ALDH1A1 P00352 3/20 0.35
CYP2A13 Q16696 1/20 0.35
HPGD P15428 1/20 0.35
HSD11B1 P28845 1/20 0.33
IRAK4 Q9NWZ3 6/20 0.33
KDM2B Q8NHM5 1/20 0.33
JAK1 P23458 1/20 0.33
KDM4E B2RXH2 2/20 0.33
IRAK2 O43187 1/20 0.32
CLK1 P49759 1/20 0.32
CLK2 P49760 1/20 0.32
IRAK1 P51617 1/20 0.32
HASPIN Q8TF76 1/20 0.32
CLK4 Q9HAZ1 1/20 0.32

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
SCHEMBL665887 0.86 SMN1; SMN2 (0.41) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL665970 0.86 SMN1; SMN2 (0.41) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL667411 0.86 SMN1; SMN2 (0.41) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL26112778 0.82 SMN1; SMN2 (0.52) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL26112782 0.82 SMN1; SMN2 (0.52) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL3168997 0.82
SCHEMBL2102406 0.81 HRH3 (0.38) SMN1; SMN2OPRL1
SCHEMBL14862483 0.79 SMN1; SMN2 (0.50) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
Ammonia Solution, Strong SCHEMBL4295582 0.79 SMN1; SMN2 (0.50) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL9425142 0.77 SMN1; SMN2 (0.54) SMN1; SMN2L3MBTL3L3MBTL1OPRL1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11939322-B2 Method for producing tetracyclic compound CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-03-26 US claimed
EP-3921319-B1 IMIDAZO [2, 1-F] [1, 2, 4] TRIAZIN-4-AMINE DERIVATIVES AS TLR7 AGONIST BEIGENE LTD (KY) 2024-03-06 EP claimed
US-20230167117-A1 IMIDAZO[2,1-F][1,2,4]TRIAZIN-4-AMINE DERIVATIVES AS TLR7 AGONIST BEONE MEDICINES I GMBH (CH) 2023-06-01 US claimed
EP-3921319-A1 IMIDAZO [2, 1-F] [1, 2, 4] TRIAZIN-4-AMINE DERIVATIVES AS TLR7 AGONIST BeiGene, Ltd. (KY) 2021-12-15 EP claimed
CN-113423708-A Imidazo [2,1-F ] [1,2,4] triazin-4-amine derivatives as TLR7 agonists 百济神州有限公司 2021-09-21 CN claimed
WO-2020160710-A1 IMIDAZO [2, 1-F] [1, 2, 4] TRIAZIN-4-AMINE DERIVATIVES AS TLR7 AGONIST BEIGENE, LTD. (KY) 2020-08-13 WO claimed
US-20200071326-A1 TAM KINASE INHIBITORS SYROS PHARMACEUTICALS INC (US) 2020-03-05 US claimed
CN-110662745-A Pyrrolopyridine derivatives, process for preparing the same, and pharmaceutical composition for preventing or treating protein kinase-associated diseases comprising the same as active ingredient 大邱庆北尖端医疗产业振兴财团 2020-01-07 CN claimed
WO-2018174650-A9 PYRROLO-PYRIDINE DERIVATIVE COMPOUND, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT FOR PREVENTION OR TREATMENT OF PROTEIN KINASE-RELATED DISEASES 재단법인 대구경북첨단의료산업진흥재단 2020-01-02 WO claimed
EP-3110812-B1 ANTI-AMYLOID COMPOUNDS CONTAINING BENZOFURAZAN TREVENTIS CORP (US) 2019-04-10 EP claimed
US-20070037853-A1 N-(3-aminopropyl)-N-{1-[1-benzyl-4-(3-chlorophenyl)-1H-imidazol-2-yl]-2-methylpropyl}morpholine-4-carboxamide and derivatives; kinesin spindle protein (KSP) inhibitors; anticarcinogenic agents; antimiotic; gene expression inhibition NOVARTIS VACCINES AND DIAGNOSTICS INC. 2007-02-15 US claimed
US-20060211698-A1 Bicyclic heteroaryl derivatives for treating viruses GENELABS, INC. 2006-09-21 US claimed
US-20060205697-A1 Novel betulin derivatives, preparation thereof and use thereof MYREXIS, INC. 2006-09-14 US claimed
WO-2006053255-A2 NOVEL BETULIN DERIVATIVES, PREPARATION THEREOF AND USE THEREOF PANACOS PHARMACEUTICALS, INC. (US) 2006-05-18 WO claimed
US-6821970-B2 USEFUL FOR TREATING DISEASES WHEREIN MODULATION OF 5-HT ACTIVITY IS DESIRED; NERVOUS SYSTEM DISORDERS PHARMACIA & UPJOHN COMPANY 2004-11-23 US claimed
US-20030225079-A1 Use of inhibitors of the EGFR-mediated signal transduction for the treatment of benign prostatic hyperplasia (BPH)/prostatic hypertrophy BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2003-12-04 US claimed
US-20020169180-A1 Bicyclic heterocycles, pharmaceutical compositions containing these compounds, their use and processes for preparing them BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2002-11-14 US claimed
EP-0781277-A1 NEUROKININ ANTAGONISTS BOEHRINGER INGELHEIM KG (DE) 1997-07-02 EP claimed
WO-1996008480-A1 NEUROKININ ANTAGONISTS BOEHRINGER INGELHEIM KG (DE) 1996-03-21 WO claimed
EP-0107261-A2 (2-((Nitropyridinyl)amino)phenyl)arylmethanones and salts, their use in medicine, pharmaceutical compositions containing them and their use in the preparation of (2-((aminopyridinyl)amino)phenyl)arylmethanones and pyrido(1,4)benzodiazepines A.H. ROBINS COMPANY, INCORPORATED (US) 1984-05-02 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 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-20200071326-A1 TAM KINASE INHIBITORS PIK3CA, MAP3K1, MAP3K5 SMN1; SMN2 4570/4885L3MBTL3 2679/4885L3MBTL1 2882/4885
US-20060205697-A1 Novel betulin derivatives, preparation thereof and use thereof BET1, PGGT1B, TMPO SMN1; SMN2 4756/4885L3MBTL3 4885/4885L3MBTL1 4879/4885
US-20070037853-A1 N-(3-aminopropyl)-N-{1-[1-benzyl-4-(3-chlorophenyl)-1H-imidazol-2-yl]-2-methylpropyl}morpholine-4-carboxamide and derivatives; kinesin spindle protein (KSP) inhibitors; anticarcinogenic agents; antimiotic; gene expression inhibition KIF5B, KIF2C, KIF18B SMN1; SMN2 1880/4885L3MBTL3 3564/4885L3MBTL1 3028/4885
US-20020169180-A1 Bicyclic heterocycles, pharmaceutical compositions containing these compounds, their use and processes for preparing them CYP11B1, ROR1, RET SMN1; SMN2 3101/4885L3MBTL3 4861/4885L3MBTL1 4708/4885
US-20230167117-A1 IMIDAZO[2,1-F][1,2,4]TRIAZIN-4-AMINE DERIVATIVES AS TLR7 AGONIST TLR7, TLR1, TLR9 SMN1; SMN2 884/4885L3MBTL3 3361/4885L3MBTL1 3110/4885
US-20060211698-A1 Bicyclic heteroaryl derivatives for treating viruses HAVCR2, ZC3HAV1, SARS1 SMN1; SMN2 2173/4885L3MBTL3 1385/4885L3MBTL1 1887/4885
US-20030225079-A1 Use of inhibitors of the EGFR-mediated signal transduction for the treatment of benign prostatic hyperplasia (BPH)/prostatic hypertrophy BPHL, EGFR, ERBB3 SMN1; SMN2 4874/4885L3MBTL3 4871/4885L3MBTL1 4865/4885
US-11939322-B2 Method for producing tetracyclic compound CYP1B1, CYP4B1, PAICS SMN1; SMN2 1226/4885L3MBTL3 3705/4885L3MBTL1 3768/4885

“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.