SCHEMBL9834330

SCHEMBL9834330

O=C1CN(c2ccccc2)C(=O)CN1c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 5/20 0.61
▸ MEN1 O00255 4/20 0.61
▸ NPC1 O15118 3/20 0.61
▸ RAB9A P51151 3/20 0.61
▸ MAPT P10636 2/20 0.54
▸ KDM4E B2RXH2 1/20 0.54
▸ GAA P10253 1/20 0.54
▸ TDP1 Q9NUW8 1/20 0.54
▸ CTSG P08311 3/20 0.52
▸ CMA1 P23946 2/20 0.52
▸ DDB1 Q16531 1/20 0.48
▸ CRBN Q96SW2 1/20 0.48
▸ ALDH1A1 P00352 2/20 0.48
▸ SIGMAR1 Q99720 1/20 0.48
▸ USP2 O75604 1/20 0.47
▸ POLB P06746 1/20 0.47
▸ HPGD P15428 1/20 0.47
▸ SMN1; SMN2 Q16637 1/20 0.47

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
SCHEMBL14541451 0.87 NPC1 (0.48) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL39842 0.84 KMT2A (0.50) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL6366167 0.82 MAPT (0.48) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL21959663 0.80 KMT2A (0.57) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL28844401 0.80 NPC1 (0.56) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL6365924 0.80 NPC1 (0.47) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL151557 0.79 MEN1 (0.56) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL19563463 0.79 KMT2A (0.55) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL156594 0.79 NPC1 (0.55) KMT2AMEN1NPC1RAB9AMAPT
SCHEMBL7745621 0.79 KMT2A (0.45) KMT2AMEN1NPC1RAB9AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-3979320-A Liquid crystal composition HODOGAYA CHEMICAL CO., LTD. (JA) 1976-09-07 — — US claimed
CN-109317194-B Catalyst for one-step synthesis of cyclic dipeptide and application thereof 安阳师范学院 2021-08-24 — — CN disclosed
CN-110234631-A For treating the composition of hypertension and/or fibrosis 维克特斯生物系统有限公司 2019-09-13 — — CN disclosed
CN-109317194-A A kind of catalyst and application for one-step synthesis Cyclic dipeptides 安阳师范学院 2019-02-12 — — CN disclosed
EP-0216745-B1 PROCESS FOR THE PREPARATION OF N-SUBSTITUTED AMINOMETHYLPHOSPHONIC ACIDS Monsanto Company (US) 1991-10-16 — — EP disclosed
EP-0216744-B1 THE COMPOUND 1,4-DIISOPROPYL-2,5-DIKETOPIPERAZINE Monsanto Company (US) 1991-08-14 — — EP disclosed
EP-0216746-B1 PROCESS TO PREPARE 2,5-DIKETOPIPERAZINES Monsanto Company (US) 1990-10-24 — — EP disclosed
US-4804499-A Process for the preparation of N-substituted aminomethylphosphonic acids MONSANTO COMPANY (US) 1989-02-14 — — US disclosed
US-4694081-A FUNGICIDES MONSANTO COMPANY (US) 1987-09-15 — — US disclosed
US-4694082-A CHEMICAL INTERMEDIATE FOR HERBICIDE MONSANTO COMPANY (US) 1987-09-15 — — US disclosed
EP-0216744-A2 The compound 1,4-diisopropyl-2,5-diketopiperazine Monsanto Company (US) 1987-04-01 — — EP disclosed
EP-0216746-A2 Process to prepare 2,5-diketopiperazines Monsanto Company (US) 1987-04-01 — — EP disclosed
EP-0216745-A1 Process for the preparation of N-substituted aminomethylphosphonic acids Monsanto Company (US) 1987-04-01 — — EP disclosed
EP-0036544-A1 Method for the preparation of substituted N-azolyl-methyl-halogeno-acetanilides BAYER AG (DE) 1981-09-30 — — EP disclosed
EP-0008057-A1 Process for the preparation of N-substituted alpha-haloacetanilides BAYER AG (DE) 1980-02-20 — — EP disclosed
US-3979320-A Liquid crystal composition HODOGAYA CHEMICAL CO., LTD. (JA) 1976-09-07 — — US disclosed
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