SCHEMBL870336

SCHEMBL870336

CCCCNC1CC(C)(C)N(O)C(C)(C)C1

nearest known ligand 0.39

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
GAA P10253 3/20 0.38
KDM4E B2RXH2 2/20 0.38
S1PR4 O95977 2/20 0.37
S1PR1 P21453 2/20 0.37
S1PR3 Q99500 2/20 0.37
GBA1 P04062 6/20 0.36
GNAI3 P08754 2/20 0.36
GNAO1 P09471 2/20 0.36
GNAI1 P63096 2/20 0.36
KMT2A Q03164 2/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
GLB1 P16278 2/20 0.35
FUCA1 P04066 1/20 0.35
S1PR5 Q9H228 1/20 0.33
MEN1 O00255 1/20 0.32
DRD2 P14416 1/20 0.31
DRD3 P35462 1/20 0.31

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
SCHEMBL7044879 0.95 GBA1 (0.43) GAAKDM4ES1PR4S1PR1S1PR3
SCHEMBL19574766 0.93 GBA1 (0.46) S1PR4S1PR1S1PR3GBA1GNAI3
SCHEMBL2963209 0.89 GAA (0.40) GAAKDM4ES1PR4S1PR1S1PR3
SCHEMBL870341 0.83 GNAI3 (0.37) S1PR4S1PR1S1PR3GBA1GNAI3
SCHEMBL870335 0.81 S1PR4 (0.37) S1PR4S1PR1S1PR3GBA1GNAI3
SCHEMBL14396773 0.81 GNAI3 (0.36) S1PR4S1PR1S1PR3GBA1GNAI3
SCHEMBL28489664 0.81 GNAI3 (0.36) S1PR4S1PR1S1PR3GBA1GNAI3
SCHEMBL2962376 0.81 GAA (0.40) GAAKDM4EKMT2AL3MBTL1
SCHEMBL18329616 0.81 GAA (0.40) GAAKDM4EKMT2AL3MBTL1
SCHEMBL5400361 0.81 GAA (0.40) GAAKDM4EKMT2AL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2984084-B1 HIGHLY EFFICIENT POLARIZING AGENTS FOR DYNAMIC NUCLEAR POLARIZATION BRUKER FRANCE S A S (FR) 2022-05-04 EP disclosed
CN-111875584-A Preparation method of multifunctional light stabilizer 宿迁市振兴化工有限公司 2020-11-03 CN disclosed
CN-103025812-B Phosphinic acid hydrazide flame retardant compositions BASF SE 2014-08-13 CN disclosed
CN-102471533-B Phenylphosphonate flame retardant compositions BASF SE 2014-07-02 CN disclosed
US-8680183-B2 Liquid stabilizer mixture BASF SE (DE) 2014-03-25 US disclosed
EP-2215156-B1 LIQUID STABILIZER MIXTURE BASF SE (DE) 2013-01-09 EP disclosed
US-20120129987-A1 LIQUID STABILIZER MIXTURE BASE SE (DE) 2012-05-24 US disclosed
EP-2445974-A1 MODIFIED ZNO NANOPARTICLES BASF SE (DE) 2012-05-02 EP disclosed
US-20120097068-A1 MODIFIED ZNO NANOPARTICLES BASE SE (DE) 2012-04-26 US disclosed
US-20120077918-A1 MIXTURES CONTAINING EFFECTIVE MATERIALS AND INORGANIC COMPOUNDS WITH HIGH SURFACE AREA BASF SE (DE) 2012-03-29 US disclosed
WO-2009068492-A2 LIQUID STABILIZER MIXTURE BASF SE (DE) 2009-06-04 WO disclosed
US-20080060775-A1 Chlorohydrin and cationic compounds having high affinity for pulp or paper CUNKLE GLEN T 2008-03-13 US disclosed
US-7312332-B2 Such as 1-butyl-3-hydroxy-1-[2-hydroxy-3-(1-oxyl-2,2,6,6-tetramethyl-piperidin-4-yloxy)-propyl]-azetidinium chloride; yellowing and discoloration prevention; ultraviolet, fluorescent and solar light stability; expanding use of high yield pulps to higher grade products CIBA SPECIALTY CHEMICALS CORPORATION (US) 2007-12-25 US disclosed
US-6989449-B1 Chlorohydrin and cationic compounds having high affinity for pulp or paper CIBA SPECIALTY CHEMICALS CORPORATION (US) 2006-01-24 US disclosed
US-20050092452-A1 Chlorohydrin and cationic compounds having high affinity for pulp or paper CUNKLE GLEN T (US) 2005-05-05 US disclosed
EP-1212486-B1 CHLOROHYDRIN AND CATIONIC COMPOUNDS HAVING HIGH AFFINITY FOR PULP OR PAPER CIBA SC HOLDING AG (CH) 2005-04-06 EP disclosed
US-6710204-B2 N-OXYL COMPOUND CONTAINED IN AN EASILY POLYMERIZABLE MATERIAL CAN BE SUFFICIENTLY DECREASED AND LOSS OF EASILY POLYMERIZABLE MATERIAL (ACRYLIC OR METHACRYLIC ACIDS OR THEIR ESTERS) IS LITTLE MITSUBISHI RAYON CO., LTD. (JP) 2004-03-23 US disclosed
US-20030078425-A1 Decreasing method of N-oxyl compound MITSUBISHI RAYON CO., LTD. (JP) 2003-04-24 US disclosed
US-5300647-A Light stabilizers for polyolefins, other polymers CIBA-GEIGY CORPORATION (US) 1994-04-05 US disclosed
EP-0309400-B1 N-acyloxy hindered amine stabilizers CIBA GEIGY AG (CH) 1994-03-02 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 (3 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-20030078425-A1 Decreasing method of N-oxyl compound NOC2L, LOXL2, VCL GAA 722/4885KDM4E 2084/4885S1PR4 4539/4885
US-20080060775-A1 Chlorohydrin and cationic compounds having high affinity for pulp or paper NISCH, HNMT, LCT GAA 1880/4885KDM4E 1242/4885S1PR4 4802/4885
US-20120097068-A1 MODIFIED ZNO NANOPARTICLES SLC39A3, SOD1, SOD3 GAA 166/4885KDM4E 1755/4885S1PR4 4650/4885

“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.