SCHEMBL8096704

SCHEMBL8096704

NC(N)=NOCc1ccccc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.53
NPC1 O15118 2/20 0.53
RAB9A P51151 2/20 0.53
SMN1; SMN2 Q16637 2/20 0.53
IDO1 P14902 1/20 0.48
AGXT P21549 1/20 0.46
TSHR P16473 2/20 0.46
HTR3A P46098 1/20 0.44
LMNA P02545 2/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
MEN1 O00255 1/20 0.42
KMT2A Q03164 1/20 0.42
SLC22A2 O15244 1/20 0.42
CA1 P00915 2/20 0.42
CA2 P00918 2/20 0.42
PARP10 Q53GL7 1/20 0.42
F2 P00734 1/20 0.41
PRSS1 P07477 1/20 0.41
PRSS2 P07478 1/20 0.41
PRSS3 P35030 1/20 0.41

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
Hydrochloric Acid SCHEMBL6747559 0.98 SMN1; SMN2 (0.51) ALDH1A1NPC1RAB9ASMN1; SMN2IDO1
Acetic Acid SCHEMBL27905814 0.91 ALDH1A1 (0.52) ALDH1A1NPC1RAB9ASMN1; SMN2L3MBTL1
SCHEMBL14257301 0.83 NPC1 (0.50) ALDH1A1NPC1RAB9ASMN1; SMN2IDO1
SCHEMBL10773629 0.79 HTR3A (0.50) ALDH1A1NPC1RAB9ASMN1; SMN2IDO1
SCHEMBL10862647 0.79 IDO1 (0.52) NPC1RAB9AIDO1AGXTHTR3A
SCHEMBL10864019 0.79 IDO1 (0.52) IDO1AGXTSLC22A2PARP10
SCHEMBL678711 0.78 MAPT (0.57) ALDH1A1NPC1RAB9ASMN1; SMN2IDO1
SCHEMBL2047156 0.78 NPC1 (0.50) ALDH1A1NPC1RAB9ASMN1; SMN2IDO1
SCHEMBL2047154 0.78 NPC1 (0.50) ALDH1A1NPC1RAB9ASMN1; SMN2IDO1
SCHEMBL408659 0.77 ALDH1A1 (0.50) ALDH1A1NPC1RAB9ASMN1; SMN2L3MBTL1

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106632132-B High activity N- oxyl anabasine analog and its preparation method and application 中国农业大学 2019-03-26 CN disclosed
EP-0748795-B1 Substituted benzyloxycarbonyl guanidines as Na+/H+ exchange inhibitors, process for their preparation, their use as medicinal or diagnostic agents as well as medicament containing them HOECHST AG (DE) 2000-08-23 EP disclosed
EP-0748795-A3 Substituted benzyloxycarbonyl guanidines as Na+/H+ exchange inhibitors, process for their preparation, their use as medicinal or diagnostic agents as well as medicament containing them HOECHST AG (DE) 1997-03-19 EP disclosed
EP-0748795-A2 Substituted benzyloxycarbonyl guanidines as Na+/H+ exchange inhibitors, process for their preparation, their use as medicinal or diagnostic agents as well as medicament containing them HOECHST AKTIENGESELLSCHAFT (DE) 1996-12-18 EP disclosed
EP-0121082-A1 Guanidin derivatives BAYER AG (DE) 1984-10-10 EP disclosed
US-4440949-A Amidinoureas WILLIAM H. RORER, INC. (US) 1984-04-03 US disclosed
US-4242339-A PHENYL-3-ALKOXYAMIDINOUREAS AND SALTS WILLIAM H. RORER, INC. (US) 1980-12-30 US disclosed
US-4242337-A PHENYL-3-ALKOXYAMIDINOUREA AND SALTS WILLIAM H. RORER, INC. (US) 1980-12-30 US disclosed
US-4242338-A PHENYLCARBAMOYLAMIDINOUREA AND SALTS WILLIAM H. RORER, INC. (US) 1980-12-30 US disclosed
US-4242340-A PHENYL-3-ALKOXYAMIDINOUREAS AND SALTS WILLIAM H. RORER, INC. (US) 1980-12-30 US disclosed
US-4218450-A Method for treatment of gastrointestinal spasmodic disease conditions or symptoms in mammals WILLIAM H. RORER, INC. (US) 1980-08-19 US disclosed
US-4169155-A AMIDINOUREAS WILLIAM H. RORER, INC. (US) 1979-09-25 US disclosed
US-4115647-A ANTISECRETORY, ANTISPASMODIC, ANTIULCEROGENIC, ANTIDIARRHEAL WILLIAM H. RORER, INC. (US) 1978-09-19 US disclosed
US-4058557-A Amidinoureas WILLIAM H. RORER, INC. (US) 1977-11-15 US disclosed