SCHEMBL181040

SCHEMBL181040

N#CC(c1ccccc1)[N+](=O)[O-]

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TRPA1 O75762 1/20 0.43
TSHR P16473 1/20 0.43
NPC1 O15118 2/20 0.40
ADAM17 P78536 1/20 0.40
ALDH1A1 P00352 5/20 0.38
LMNA P02545 2/20 0.38
GSR P00390 1/20 0.38
AKR1C3 P42330 1/20 0.38
AKR1C1 Q04828 1/20 0.38
HPGD P15428 3/20 0.35
NPSR1 Q6W5P4 3/20 0.35
KMT2A Q03164 3/20 0.35
KDM4E B2RXH2 2/20 0.35
MAPT P10636 2/20 0.35
TDP1 Q9NUW8 2/20 0.35
L3MBTL1 Q9Y468 2/20 0.34
ALOX12 P18054 1/20 0.34
HTT P42858 2/20 0.34
USP2 O75604 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34

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
SCHEMBL153030 0.81 NPC1 (0.41) NPC1ADAM17ALDH1A1LMNAGSR
SCHEMBL8388639 0.75 SGMS2 (0.57) TSHRLMNAHPGDKMT2AHTT
SCHEMBL6652366 0.75 PRSS1 (0.36) TSHRALDH1A1GSRMAPTL3MBTL1
SCHEMBL19356869 0.73 LMNA (0.44) TSHRNPC1ADAM17ALDH1A1LMNA
SCHEMBL8967425 0.72 EGFR (0.38) TSHRLMNAHPGDKMT2AKDM4E
SCHEMBL5752626 0.72 ALDH1A1 (0.46) TSHRALDH1A1HPGDTDP1HTT
SCHEMBL446453 0.71 CES2 (0.43) TRPA1NPC1ADAM17ALDH1A1LMNA
SCHEMBL2163543 0.71 GSR (0.50) TRPA1TSHRNPC1ADAM17ALDH1A1
SCHEMBL27646281 0.71 GSR (0.50) TRPA1TSHRNPC1ADAM17ALDH1A1
SCHEMBL407211 0.71 GSR (0.42) TRPA1TSHRNPC1ADAM17ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1437749-B1 ELECTROLYTE SOLUTION FOR DRIVING ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR RUBYCON CORP (JP) 2013-07-17 EP claimed
US-7539006-B2 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2009-05-26 US claimed
US-20070029529-A1 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor KOMATSU AKIHIKO 2007-02-08 US claimed
US-20040245105-A1 Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2004-12-09 US claimed
EP-1437749-A1 ELECTROLYTE SOLUTION FOR DRIVING ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR Rubycon Corporation (JP) 2004-07-14 EP claimed
EP-3845515-B1 PRODUCTION METHOD FOR CRYSTAL OF REDUCED COENZYME Q10 HAVING EXCELLENT STABILITY KANEKA CORP (JP) 2025-11-12 EP disclosed
CN-117715903-A Cereblon binding compounds, compositions thereof, and methods for their use in therapy 新基公司 2024-03-15 CN disclosed
CN-117561249-A Cereblon binding compounds, compositions thereof, and methods for their use in therapy 细胞基因公司 2024-02-13 CN disclosed
US-11773043-B2 Systems and methods for producing coenzyme Q10 Inner Mongolia Kingdomway Pharmaceutical Co., Ltd. (CN) 2023-10-03 US disclosed
CN-110944970-B For the production of coenzyme Q 10 Systems and methods of (1) 内蒙古金达威药业有限公司 2023-08-01 CN disclosed
US-11498893-B2 Production method for crystal of reduced coenzyme Q10 having excellent stability KANEKA CORPORATION (JP) 2022-11-15 US disclosed
US-11453633-B2 Production method for crystal of reduced coenzyme Q10 having excellent stability KANEKA CORPORATION (JP) 2022-09-27 US disclosed
EP-0078709-B1 PREPARATION OF NITROARALKYL CYANIDES AND DERIVATIVES THEREOF ETHYL CORPORATION (US) 1986-10-01 EP disclosed
US-4581463-A Nucleophilic substitution process combined with additional reaction steps ETHYL CORPORATION (US) 1986-04-08 US disclosed
EP-0077662-B1 PREPARATION OF NITROARYLACETIC ACID ESTERS AND DERIVATIVES THEREOF ETHYL CORPORATION (US) 1985-10-02 EP disclosed
US-4502996-A Nucleophilic substitution process ETHYL CORPORATION (US) 1985-03-05 US disclosed
US-4502995-A Nucleophilic substitution process ETHYL CORPORATION (US) 1985-03-05 US disclosed
EP-0078709-A2 Preparation of nitroaralkyl cyanides and derivatives thereof ETHYL CORPORATION (US) 1983-05-11 EP disclosed
EP-0077662-A1 Preparation of nitroarylacetic acid esters and derivatives thereof ETHYL CORPORATION (US) 1983-04-27 EP disclosed
US-4064136-A FROM A NITRILE, AN ALCOHOL AND ORTHO-SUBSTITUTED AROMATIC AMINE CIBA-GEIGY AG (CH) 1977-12-20 US disclosed