SCHEMBL550670

SCHEMBL550670

Cc1cc(CCl)ccc1[N+](=O)[O-]

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.51
TSHR P16473 6/20 0.50
HSD17B10 Q99714 1/20 0.47
NR3C1 P04150 1/20 0.46
PGR P06401 1/20 0.46
AR P10275 1/20 0.46
CYP3A4 P08684 2/20 0.46
HPGD P15428 1/20 0.45
ALDH1A1 P00352 3/20 0.43
L3MBTL1 Q9Y468 4/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
RAB9A P51151 2/20 0.43
NPC1 O15118 1/20 0.43
BLM P54132 1/20 0.42
RECQL P46063 1/20 0.42
LMNA P02545 2/20 0.41
KDM4E B2RXH2 1/20 0.41
MAPK1 P28482 1/20 0.40
POLB P06746 1/20 0.40
TDP1 Q9NUW8 1/20 0.40

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
SCHEMBL8601774 0.89 TSHR (0.51) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL1492448 0.85 ALDH1A1 (0.55) MAPTTSHRHSD17B10CYP3A4HPGD
SCHEMBL13344094 0.83 MAPT (0.53) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL18138464 0.83 MAPT (0.53) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL31747006 0.81 TSHR (0.54) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL713941 0.81 TSHR (0.54) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL7988274 0.81 MAPT (0.51) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL508871 0.81 MAPT (0.51) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL27926845 0.81 MAPT (0.51) MAPTTSHRHSD17B10NR3C1PGR
SCHEMBL10662837 0.81 MAPT (0.51) MAPTTSHRHSD17B10NR3C1PGR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12606564-B2 Adenosine receptor antagonist compounds ILDONG PHARMACEUTICAL CO., LTD. (KR) 2026-04-21 US disclosed
US-20260035361-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) SHANGHAI DEGRON BIOMEDICAL TECH CO LTD (CN) 2026-02-05 US disclosed
EP-4626880-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) Shanghai Degron Biomedical Technology Co., Ltd. (CN) 2025-10-08 EP disclosed
CN-116425756-B Adenosine receptor antagonist compounds and uses thereof 日东制药株式会社 2025-05-13 CN disclosed
WO-2024242530-A1 COMPOUND FOR NEUROPROTECTION, OR TREATING DISEASES RELATED TO ALPHA-SYNUCLEIN AND/OR NEURO-INFLAMMATION YUNOVIA CO., LTD. (KR) 2024-11-28 WO disclosed
CN-114829363-B Adenosine receptor antagonist compounds 日东制药株式会社 2024-10-01 CN disclosed
WO-2024114639-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) SHANGHAI DEGRON BIOMEDICAL TECHNOLOGY CO., LTD. (CN) 2024-06-06 WO disclosed
US-20240041888-A1 PREVENTION AND/OR TREATMENT OF CNS DISORDERS ILDONG PHARMACEUTICAL CO., LTD. (KR) 2024-02-08 US disclosed
US-11806350-B2 Prevention and/or treatment of CNS disorders ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-11-07 US disclosed
US-11806350-B2 Prevention and/or treatment of CNS disorders ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-11-07 US disclosed
US-6197965-B1 POLYARYLALKYLAMINO-SUBSTITUED PYRIDINE DERIVATIVES; DRUGS, MEDICINE, DIAGNOSTICS ISIS PHARMACEUTICALS, INC. 2001-03-06 US disclosed
EP-0817787-A4 NITROGENOUS MACROCYCLIC COMPOUNDS ISIS PHARMACEUTICALS INC (US) 2000-09-13 EP disclosed
WO-1998010286-A1 METHODS FOR PROCESSING CHEMICAL COMPOUNDS HAVING REACTIVE FUNCTIONAL GROUPS ISIS PHARMACEUTICALS, INC. (US) 1998-03-12 WO disclosed
EP-0817787-A1 NITROGENOUS MACROCYCLIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 1998-01-14 EP disclosed
WO-1996030377-A1 NITROGENOUS MACROCYCLIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 1996-10-03 WO disclosed
EP-0369627-B1 Pyrimidinedione derivative compounds, method of producing the same and antiarrythmic agents containing the same MITSUI TOATSU CHEMICALS (JP) 1994-12-21 EP disclosed
US-5008267-A Pyrimidinedione compounds, method of producing the same and antiarrythmic agents containing the same MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1991-04-16 US disclosed
EP-0369627-A2 Pyrimidinedione derivative compounds, method of producing the same and antiarrythmic agents containing the same MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-05-23 EP disclosed
EP-0000718-B1 QUINAZOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION, PHARMACEUTICAL PREPARATIONS AND THEIR PREPARATION F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1982-03-24 EP disclosed
EP-0000718-A2 Quinazoline derivatives, process for their preparation, pharmaceutical preparations and their preparation F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1979-02-21 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 (4 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-20240041888-A1 PREVENTION AND/OR TREATMENT OF CNS DISORDERS ADORA2A, ADORA1, ADORA2B MAPT 615/4885TSHR 620/4885HSD17B10 4713/4885
US-12606564-B2 Adenosine receptor antagonist compounds ADORA2A, ADORA1, ADORA2B MAPT 3225/4885TSHR 136/4885HSD17B10 3252/4885
US-11806350-B2 Prevention and/or treatment of CNS disorders ADORA2A, ADORA1, ADORA2B MAPT 615/4885TSHR 620/4885HSD17B10 4713/4885
US-20260035361-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) ELAVL1, ELAVL3, HNRNPL MAPT 624/4885TSHR 1113/4885HSD17B10 2166/4885

“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.