SCHEMBL7110422

SCHEMBL7110422

CC(C)(C)OC(=O)C(O)CCN

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NOS1 P29475 2/20 0.36
NOS3 P29474 1/20 0.36
NOS2 P35228 1/20 0.36
GABRR1 P24046 2/20 0.35
KMT2A Q03164 2/20 0.33
MEN1 O00255 1/20 0.33
GAA P10253 1/20 0.33
CPB2 Q96IY4 1/20 0.33
CTSK P43235 5/20 0.32
AAK1 Q2M2I8 1/20 0.32
LMNA P02545 1/20 0.31
CYP2D6 P10635 1/20 0.31
CA1 P00915 1/20 0.31
CA2 P00918 1/20 0.31
CA7 P43166 1/20 0.31
DGAT1 O75907 1/20 0.30
GABBR2 O75899 1/20 0.30
GABBR1 Q9UBS5 1/20 0.30
HDAC3 O15379 1/20 0.30
HDAC1 Q13547 1/20 0.30

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
SCHEMBL6797401 1.00 NOS1 (0.36) NOS1NOS3NOS2GABRR1KMT2A
SCHEMBL9417498 0.91 CA12 (0.34) NOS1NOS3NOS2GABRR1KMT2A
SCHEMBL2177004 0.88 CPB2 (0.38) NOS1NOS3NOS2KMT2AMEN1
SCHEMBL133019 0.86 CPB2 (0.44) NOS1NOS3NOS2KMT2AMEN1
SCHEMBL2567893 0.85 CPB2 (0.46) NOS1NOS3NOS2KMT2AMEN1
SCHEMBL6799320 0.83 NOS1 (0.35) NOS1NOS3NOS2GABRR1KMT2A
SCHEMBL5667907 0.83 NOS1 (0.35) NOS1NOS3NOS2GABRR1KMT2A
Methylamine SCHEMBL28388761 0.82 NOS1 (0.39) NOS1NOS3NOS2KMT2AMEN1
SCHEMBL28058283 0.82 KMT2A (0.36) NOS1NOS3NOS2GABRR1KMT2A
SCHEMBL9242626 0.81 GPR84 (0.42) NOS1NOS3NOS2KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4658668-A2 OCCIDIOFUNGIN ANALOGS AND METHODS OF MAKING AND USING The Texas A&M University System (US) 2025-12-10 EP disclosed
WO-2024163850-A2 OCCIDIOFUNGIN ANALOGS AND METHODS OF MAKING AND USING THE TEXAS A&M UNIVERSITY SYSTEM (US) 2024-08-08 WO disclosed
EP-3873457-B1 ISOSORBIDE-5-MONONITRATE DERIVATIVES AS POTENTIATORS OF VASODILATORY RELEASE OF NITRIC OXIDE IN HYPOXIA FOR THE TREATMENT OF CARDIOVASCULAR DISEASES COEURATIVE INC (US) 2024-02-07 EP disclosed
US-11779560-B2 Methods of using nitric oxide donor compounds for treatment of COVID-19 and other infectious diseases COEURATIVE, INC. (US) 2023-10-10 US disclosed
EP-4126221-A2 NOVEL METHODS OF USING NITRIC OXIDE DONOR COMPOUNDS FOR TREATMENT OF COVID-19 AND OTHER INFECTIOUS DISEASES Coeurative, Inc. (US) 2023-02-08 EP disclosed
CN-115474429-A Novel methods of treating COVID-19 and other infectious diseases using nitric oxide donor compounds 合作股份有限公司 2022-12-13 CN disclosed
US-20210346335-A1 METHODS OF USING NITRIC OXIDE DONOR COMPOUNDS FOR TREATMENT OF COVID-19 AND OTHER INFECTIOUS DISEASES COEURATIVE, INC. (US) 2021-11-11 US disclosed
WO-2021202317-A2 NOVEL METHODS OF USING NITRIC OXIDE DONOR COMPOUNDS FOR TREATMENT OF COVID-19 AND OTHER INFECTIOUS DISEASES COEURATIVE, INC. (US) 2021-10-07 WO disclosed
EP-3873457-A1 NOVEL COMPOUNDS USEFUL FOR TREATING CARDIOVASCULAR DISEASES Coeurative, Inc. (US) 2021-09-08 EP disclosed
CN-113226301-A Novel compounds suitable for the treatment of cardiovascular diseases 科由拉特夫公司 2021-08-06 CN disclosed
EP-1347784-A2 SIMULTANEOUS DUAL ISOTOPE IMAGING OF CARDIAC PERFUSION AND CARDIAC INFLAMMATION Bristol-Myers Squibb Pharma Company (US) 2003-10-01 EP disclosed
CN-1098278-C Cinnamic acid derivative SEIKAGAKU KOGYO CO LTD (JP) 2003-01-08 CN disclosed
CN-1090637-C Crosslinked cinnamic acid hyaluronic acid derivatives and process for producing the same SEIKAGAKU KOGYO CO LTD (JP) 2002-09-11 CN disclosed
WO-2002036173-A2 SIMULTANEOUS DUAL ISOTOPE IMAGING OF CARDIAC PERFUSION AND CARDIAC INFLAMMATION BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2002-05-10 WO disclosed
EP-0713859-B1 Cinnamic acid derivatives, photocrosslinkable cinnamic acid-polymer derivative and crosslinked cinnamic acid polymer derivatives SEIKAGAKU KOGYO CO LTD (JP) 2000-08-30 EP disclosed
US-6107410-A Cinnamic acid derivative SEIKAGAKU CORPORATION (JP) 2000-08-22 US disclosed
CN-1245812-A Cinnamic acid derivative SEIKAGAKU KOGYO CO LTD (JP) 2000-03-01 CN disclosed
US-6025444-A HYALURONIC ACID POLYSACCHARIDE DERIVATIVE; PHOTODIMERIZABLE, CROSSLINKABLE SEIKAGAKU KOGYO KABUSHIKI KAISHA (SEIKAGAKU CORPORATION) (JP) 2000-02-15 US disclosed
CN-1133834-A cinnamic acid derivatives SEIKAGAKU KOGYO CO LTD (JP) 1996-10-23 CN disclosed
EP-0713859-A2 Cinnamic acid derivatives, photocrosslinkable cinnamic acid-polymer derivative and crosslinked cinnamic acid polymer derivatives SEIKAGAKU KOGYO KABUSHIKI KAISHA (SEIKAGAKU CORPORATION) (JP) 1996-05-29 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 (2 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-11779560-B2 Methods of using nitric oxide donor compounds for treatment of COVID-19 and other infectious diseases NOS2, NOS1, NOS3 NOS1 2/4885NOS3 3/4885NOS2 1/4885
US-20210346335-A1 METHODS OF USING NITRIC OXIDE DONOR COMPOUNDS FOR TREATMENT OF COVID-19 AND OTHER INFECTIOUS DISEASES NOS2, NOS1, NOS3 NOS1 2/4885NOS3 3/4885NOS2 1/4885

“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.