SCHEMBL7114121

SCHEMBL7114121

Brc1ccc(-c2nnc(-c3cccc4ccccc34)o2)cc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ RAB9A P51151 11/20 0.67
▸ NPC1 O15118 9/20 0.67
▸ TSHR P16473 7/20 0.67
▸ ALDH1A1 P00352 4/20 0.67
▸ SMN1; SMN2 Q16637 3/20 0.67
▸ TP53 P04637 3/20 0.67
▸ MAPT P10636 2/20 0.67
▸ HPGD P15428 1/20 0.67
▸ KDM4E B2RXH2 4/20 0.63
▸ HSD17B10 Q99714 4/20 0.63
▸ CYP1A2 P05177 2/20 0.63
▸ CYP2C19 P33261 1/20 0.63
▸ ATM Q13315 1/20 0.63
▸ MEN1 O00255 1/20 0.55
▸ KMT2A Q03164 1/20 0.55
▸ ALOX15 P16050 2/20 0.54
▸ ATR Q13535 1/20 0.49
▸ BCHE P06276 1/20 0.49
▸ ACHE P22303 1/20 0.49
▸ NPSR1 Q6W5P4 1/20 0.48

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
SCHEMBL19932454 0.87 RAB9A (0.67) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL29355388 0.87 RAB9A (0.66) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL4333750 0.87 RAB9A (0.66) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL29408668 0.85 ALOX15 (0.69) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL186871 0.85 ALOX15 (0.69) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL12177603 0.84 RAB9A (0.63) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL1720737 0.83 HSD17B10 (0.70) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL13134513 0.83 RAB9A (0.62) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL9346519 0.83 KDM4E (0.62) RAB9ANPC1TSHRALDH1A1SMN1; SMN2
SCHEMBL9341645 0.83 ALDH1A1 (0.62) RAB9ANPC1TSHRALDH1A1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108947926-A It is a kind of based on pyrene-oxadiazole derivatives bipolarity compound and its application 瑞声科技(南京)有限公司 2018-12-07 — — CN disclosed
WO-2018131877-A1 DELAYED FLUORESCENCE COMPOUND, ORGANIC ELECTRIC ELEMENT USING SAME, AND ELECTRONIC DEVICE USING SAME 덕산네오룩스 주식회사 2018-07-19 — — WO disclosed
US-20150275076-A1 Non-crystallizable Pi-conjugated Molecular Glass Mixtures, Charge Transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications Molaire Consulting 2015-10-01 — — US disclosed
US-20150275076-A1 Non-crystallizable Pi-conjugated Molecular Glass Mixtures, Charge Transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications Molaire Consulting 2015-10-01 — — US disclosed
US-6517958-B1 Silsesquioxane compounds having hole transport, electron transport and/or emissive material moieties; luminescence efficiency, brilliance, turn on voltage, longevity CANON KABUSHIKI KAISHA (JP) 2003-02-11 — — US disclosed
WO-2002005971-A1 ORGANIC-INORGANIC HYBRID LIGHT EMITTING DEVICES (HLED) CANON KABUSHIKI KAISHA (JP) 2002-01-24 — — WO disclosed
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