SCHEMBL392679

SCHEMBL392679

CCOC(=O)Cc1ccc(N)c([N+](=O)[O-])c1

nearest known ligand 0.51

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.51
MEN1 O00255 3/20 0.50
KMT2A Q03164 3/20 0.50
HTT P42858 1/20 0.50
TSHR P16473 1/20 0.50
MAPT P10636 6/20 0.46
TDP1 Q9NUW8 3/20 0.45
ALDH1A1 P00352 3/20 0.45
POLB P06746 1/20 0.45
CYP3A4 P08684 1/20 0.45
ALOX15 P16050 1/20 0.45
KDM4E B2RXH2 1/20 0.44
NPC1 O15118 1/20 0.44
GAA P10253 1/20 0.44
MAPK1 P28482 1/20 0.44
CYP1A2 P05177 1/20 0.43
CYP2C9 P11712 1/20 0.43
CYP2C19 P33261 1/20 0.43

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
SCHEMBL30848995 1.00 LMNA (0.51) LMNAMEN1KMT2AHTTTSHR
SCHEMBL14684937 0.87 LMNA (0.43) LMNAMEN1KMT2AHTTMAPT
SCHEMBL30224794 0.87 AKR1C3 (0.41) LMNAMEN1KMT2AHTTTSHR
SCHEMBL7425083 0.86 ALDH1A1 (0.57) LMNAMEN1KMT2AHTTTSHR
SCHEMBL5201986 0.84 LMNA (0.49) LMNAMEN1KMT2AHTTMAPT
SCHEMBL1694828 0.84 MAPT (0.49) LMNAMEN1KMT2AHTTTSHR
SCHEMBL5092015 0.84 LMNA (0.49) LMNAMEN1KMT2AHTTMAPT
SCHEMBL31085600 0.83 LMNA (0.53) LMNAMEN1KMT2AHTTMAPT
SCHEMBL31085599 0.83 LMNA (0.53) LMNAMEN1KMT2AHTTMAPT
SCHEMBL15270721 0.83 LMNA (0.53) LMNAMEN1KMT2AHTTMAPT

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-20250289785-A1 INDOLE DERIVATIVE, METHOD FOR PREPARING SAME, AND USE THEREOF MITOIMMUNE THERAPEUTICS INC. (KR) 2025-09-18 US disclosed
US-20250172566-A1 SACCHARIDE SENSING SYSTEMS Carbometrics Limited (GB) 2025-05-29 US disclosed
US-20250122155-A1 NOVEL INDOLE DERIVATIVE, PHARMACEUTICAL COMPOSITION COMPRISING SAME, AND USE THEREOF MITOIMMUNE THERAPEUTICS INC. (KR) 2025-04-17 US disclosed
EP-4469803-A1 SACCHARIDE SENSING SYSTEMS Carbometrics Limited (GB) 2024-12-04 EP disclosed
CN-118847245-A Synthesis method of bromoalkyl substituted quinoxaline 烟台宁远药业有限公司 2024-10-29 CN disclosed
EP-4382524-A1 INDOLE DERIVATIVE, METHOD FOR PREPARING SAME, AND USE THEREOF MitoImmune Therapeutics Inc. (KR) 2024-06-12 EP disclosed
EP-4382523-A1 NOVEL INDOLE DERIVATIVE, PHARMACEUTICAL COMPOSITION COMPRISING SAME, AND USE THEREOF MitoImmune Therapeutics Inc. (KR) 2024-06-12 EP disclosed
CN-117794917-A Novel indole derivatives, pharmaceutical compositions containing the same and uses thereof 水疗免疫疗法有限公司 2024-03-29 CN disclosed
CN-117794922-A Indole derivatives, process for their preparation and their use 水疗免疫疗法有限公司 2024-03-29 CN disclosed
CN-114478497-B Arylalkyl acid GLP-1 receptor agonists and uses thereof 杭州中美华东制药有限公司 2023-10-20 CN disclosed
WO-2005123050-A2 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-12-29 WO disclosed
US-20050282805-A1 thrombotic or an inflammatory disorders; improved factor XIa and/or plasma kallikrein inhibitory activity and selectivity, dosage requirment, costs or feasibility, side effect reduction; 4-(aminomethyl)-N-[2-phenyl-1-(4-pyridin-2-yl-1H-imidazol-2-yl)ethyl]-trans-cyclohexanecarboxamide BRISTOL-MYERS SQUIBB COMPANY 2005-12-22 US disclosed
EP-1007037-A4 ANTITHROMBOTIC AGENTS LILLY CO ELI (US) 2004-10-06 EP disclosed
US-6677369-B2 CARBOXIMIDAMIDE DERIVATIVE ANTICOAGULANTS INHIBIT FACTOR XA ELI LILLY AND COMPANY 2004-01-13 US disclosed
US-20030195223-A1 An anticoagulant, blood inhibitor of factor Xa, a N1-amidinebenzoyl- N2-benzoyl-1,2-benzenediamine derivatives; chemical intermediates BEIGHT DOUGLAS WADE (US) 2003-10-16 US disclosed
US-6417200-B1 BLOOD COAGULATION FACTOR XA IN MAMMALS ELI LILLY AND COMPANY 2002-07-09 US disclosed
EP-1007037-A1 ANTITHROMBOTIC AGENTS ELI LILLY AND COMPANY (US) 2000-06-14 EP disclosed
WO-1999000127-A1 ANTITHROMBOTIC AGENTS ELI LILLY AND COMPANY (US) 1999-01-07 WO disclosed
US-4767769-A HISTAMINE-H2 ANTAGONISTS THE BOOTS COMPANY PLC (GB) 1988-08-30 US disclosed
EP-0172631-A1 Therapeutic agents The Boots Company PLC (GB) 1986-02-26 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 (5 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-20030195223-A1 An anticoagulant, blood inhibitor of factor Xa, a N1-amidinebenzoyl- N2-benzoyl-1,2-benzenediamine derivatives; chemical intermediates F12, F11, F2 LMNA 415/4885MEN1 611/4885KMT2A 2684/4885
US-20250289785-A1 INDOLE DERIVATIVE, METHOD FOR PREPARING SAME, AND USE THEREOF AIFM2, AIFM1, HMOX1 LMNA 1625/4885MEN1 813/4885KMT2A 4547/4885
US-20250172566-A1 SACCHARIDE SENSING SYSTEMS GALE, SLC2A8, SLC2A4 LMNA 4421/4885MEN1 1771/4885KMT2A 4482/4885
US-20250122155-A1 NOVEL INDOLE DERIVATIVE, PHARMACEUTICAL COMPOSITION COMPRISING SAME, AND USE THEREOF AIFM2, AIFM1, FECH LMNA 2515/4885MEN1 1362/4885KMT2A 4608/4885
US-20050282805-A1 thrombotic or an inflammatory disorders; improved factor XIa and/or plasma kallikrein inhibitory activity and selectivity, dosage requirment, costs or feasibility, side effect reduction; 4-(aminomethyl)-N-[2-phenyl-1-(4-pyridin-2-yl-1H-imidazol-2-yl)ethyl]-trans-cyclohexanecarboxamide F11, TFPI, F12 LMNA 500/4885MEN1 1744/4885KMT2A 290/4885

“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.