SCHEMBL6160201

SCHEMBL6160201

[CH2]CC=Cc1ccccn1

nearest known ligand 0.62

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 3/20 0.62
▸ RAB9A P51151 3/20 0.62
▸ MEN1 O00255 2/20 0.62
▸ KMT2A Q03164 2/20 0.62
▸ ATM Q13315 1/20 0.62
▸ GRM4 Q14833 1/20 0.44
▸ NR4A1 P22736 1/20 0.44
▸ MAOA P21397 1/20 0.42
▸ TDP1 Q9NUW8 1/20 0.42
▸ PTGS1 P23219 1/20 0.41
▸ PTGS2 P35354 1/20 0.41
▸ ALDH1A1 P00352 1/20 0.40
▸ MAPT P10636 1/20 0.40
▸ NFE2L2 Q16236 1/20 0.40
▸ HSP90AA1 P07900 1/20 0.40
▸ G6PC1 P35575 1/20 0.40

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
SCHEMBL6556168 1.00 NPC1 (0.62) NPC1RAB9AMEN1KMT2AATM
SCHEMBL1165357 0.81 NPC1 (0.60) NPC1RAB9AMEN1KMT2AATM
Hydrochloric Acid SCHEMBL29141002 0.79 NPC1 (0.58) NPC1RAB9AMEN1KMT2AATM
SCHEMBL6140060 0.78 RAB9A (0.62) NPC1RAB9AMEN1KMT2AATM
SCHEMBL2989454 0.78 NPC1 (0.62) NPC1RAB9AMEN1KMT2AATM
SCHEMBL31124655 0.78 NPC1 (0.62) NPC1RAB9AMEN1KMT2AATM
SCHEMBL10801184 0.78 NPC1 (0.62) NPC1RAB9AMEN1KMT2AATM
SCHEMBL11105985 0.78 NPC1 (0.62) NPC1RAB9AMEN1KMT2AATM
SCHEMBL256048 0.78 NPC1 (0.62) NPC1RAB9AMEN1KMT2AATM
SCHEMBL11105983 0.78 NPC1 (0.62) NPC1RAB9AMEN1KMT2AATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1505156-B1 Process for the enantioselective preparation of secondary alcohols by lipase catalysed solvolysis of the corresponding acetoacetic acid ester CONSORTIUM ELEKTROCHEM IND (DE) 2005-12-07 — — EP disclosed
EP-1505156-A1 Process for the enantioselective preparation of secondary alcohols by lipase catalysed solvolysis of the corresponding acetoacetic acid ester Consortium für elektrochemische Industrie GmbH (DE) 2005-02-09 — — EP disclosed
CN-1188401-C Heterocyclic amide compound and its pharmaceutical use MITSUBISHI PHARMACEUTICAL CO L (JP) 2005-02-09 — — CN disclosed
EP-0826671-B1 HETEROCYCLIC AMIDE COMPOUNDS AND MEDICINAL USE OF THE SAME MITSUBISHI PHARMA CORP (JP) 2004-12-29 — — EP disclosed
CN-1131210-C Heterocyclic amide compound and medical use thereof MITSUBISHI SEIYAKU CO LTD (JP) 2003-12-17 — — CN disclosed
US-6528514-B1 Pyrimidin-4-one-5-amino-3-alkylcarboxamidomethyl compounds WELFIDE CORPORATION (JP) 2003-03-04 — — US disclosed
CN-1304931-A Heterocyclic amide compound and medical use thereof EFUKU CO LTD (JP) 2001-07-25 — — CN disclosed
EP-1062949-A1 IgE ANTIBODY PRODUCTION INHIBITORS AND AUTOIMMUNE DISEASES INHIBITORS Welfide Corporation (JP) 2000-12-27 — — EP disclosed
US-5948785-A USEFUL AS CHYMASE INHIBITORS AND CAN BE EFFECTIVE FOR THE PROPHYLAXIS AND TREATMENT OF VARIOUS DISEASES CAUSED BY CHYMASE, SUCH AS THOSE CAUSED BY ANGIOTENSIN II. THE GREEN CROSS CORPORATION (JP) 1999-09-07 — — US disclosed
CN-1188472-A Heterocyclic amide compound and medical use thereof GREEN CROSS CORP (JP) 1998-07-22 — — CN disclosed
EP-0826671-A1 HETEROCYCLIC AMIDE COMPOUNDS AND MEDICINAL USE OF THE SAME THE GREEN CROSS CORPORATION (JP) 1998-03-04 — — EP disclosed
Send feedback