SCHEMBL2372027

SCHEMBL2372027

O=C(O)CCCCCCCCCCC[N+](=O)[O-]

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.65
MEN1 O00255 3/20 0.65
KMT2A Q03164 3/20 0.65
BLM P54132 1/20 0.65
HBB P68871 1/20 0.65
HIF1A Q16665 1/20 0.65
TSHR P16473 5/20 0.57
NFKB1 P19838 1/20 0.57
PMP22 Q01453 1/20 0.57
ALDH1A1 P00352 4/20 0.50
GPR84 Q9NQS5 7/20 0.48
FFAR1 O14842 2/20 0.48
FFAR4 Q5NUL3 2/20 0.48
HSD17B10 Q99714 2/20 0.46
CYP1A2 P05177 1/20 0.46
CYP2D6 P10635 1/20 0.46
MAPT P10636 1/20 0.46
CYP2C9 P11712 1/20 0.46
CYP2C19 P33261 1/20 0.46
PPARG P37231 6/20 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
SCHEMBL504353 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL2371134 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL2370652 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL1119124 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL2371891 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL2371874 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL5828245 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL2380101 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL11701621 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB
SCHEMBL2371273 1.00 LMNA (0.65) LMNAMEN1KMT2ABLMHBB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7732625-B2 Colorant compounds XEROX CORPORATION (US) 2010-06-08 US claimed
US-7311767-B2 Forming a salt of a liquid phase change ink carrier of stearyl stearamide, an amine substituted Xanthene, acridine, anthracene or thioxanthene chromogen, and a metal salt capable of forming a compound with two chromogens XEROX CORPORATION (US) 2007-12-25 US claimed
US-7033424-B2 Phase change inks XEROX CORPORATION (US) 2006-04-25 US claimed
US-20060021546-A1 Processes for preparing phase change inks XEROX CORPORATION 2006-02-02 US claimed
US-20060016369-A1 PHASE CHANGE INKS XEROX CORPORATION 2006-01-26 US claimed
US-20030157538-A1 Nucleic acid biosensor diagnostics KRULL ULRICH J (CA) 2003-08-21 US claimed
US-20130039956-A1 USE OF NITROCARBOXYLIC ACIDS FOR THE TREATMENT, DIAGNOSIS AND PROPHYLAXIS OF AGGRESSIVE HEALING PATTERNS Dietz, Ulrich (DE) 2013-02-14 US disclosed
EP-2547322-A2 USE OF NITROCARBOXYLIC ACIDS FOR THE TREATMENT, DIAGNOSIS AND PROPHYLAXIS OF AGGRESSIVE HEALING PATTERNS Dietz, Ulrich (DE) 2013-01-23 EP disclosed
WO-2011113507-A2 USE OF NITROCARBOXYLIC ACIDS FOR THE TREATMENT, DIAGNOSIS AND PROPHYLAXIS OF AGGRESSIVE HEALING PATTERNS DIETZ ULRICH (DE) 2011-09-22 WO disclosed
EP-1956054-B1 Phase change ink XEROX CORP (US) 2010-11-24 EP disclosed
US-7732625-B2 Colorant compounds XEROX CORPORATION (US) 2010-06-08 US disclosed
EP-1958993-A1 Phase change inks containing colorant compounds Xerox Corporation (US) 2008-08-20 EP disclosed
EP-1956054-A2 Colorant compounds Xerox Corporation (US) 2008-08-13 EP disclosed
US-5137929-A Additives which stabilize hydrohalocarbon blowing agent in polyurethane and polyisocyanurate foam formulations during polymerization ALLIED-SIGNAL INC. (US) 1992-08-11 US disclosed
US-4961867-A Process for preventing corrosion of metals by contacting them with compositions prepared from amino substituted pyrazines and carboxylic acids carboxylic acid anhydrides, carboxylic acid, esters or carboxylic acid halides THE DOW CHEMICAL COMPANY (US) 1990-10-09 US disclosed
US-4957640-A Corrosion prevention with compositions prepared from organic fatty amines and nitrogen-containing aromatic heterocyclic compounds THE DOW CHEMICAL COMPANY (US) 1990-09-18 US disclosed
US-4861884-A OIL WELL CORROSION INHIBITOR THE DOW CHEMICAL COMPANY (US) 1989-08-29 US disclosed
US-4765839-A PAVING THE DOW CHEMICAL COMPANY (US) 1988-08-23 US disclosed
US-4761473-A CORROSION RESISTANCE OF OIL OR GAS WELLS THE DOW CHEMICAL COMPANY (US) 1988-08-02 US disclosed
US-4035400-A Preparation of omega-nitroalkanoic acids TEXACO INC. (US) 1977-07-12 US 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 (1 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-20130039956-A1 USE OF NITROCARBOXYLIC ACIDS FOR THE TREATMENT, DIAGNOSIS AND PROPHYLAXIS OF AGGRESSIVE HEALING PATTERNS NOS1, NOS2, NOS3 LMNA 3624/4885MEN1 4792/4885KMT2A 4163/4885

“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.