SCHEMBL230643

SCHEMBL230643

NCC(N)Cc1ccccn1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GRIN2D O15399 1/20 0.59
GRIN3B O60391 1/20 0.59
GRIN1 Q05586 1/20 0.59
GRIN2A Q12879 1/20 0.59
GRIN2B Q13224 1/20 0.59
GRIN2C Q14957 1/20 0.59
GRIN3A Q8TCU5 1/20 0.59
HRH1 P35367 2/20 0.53
FDPS P14324 1/20 0.49
PTPRA P18433 1/20 0.49
DPP4 P27487 1/20 0.46
MAPT P10636 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
LIN28A Q9H9Z2 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
MAOA P21397 2/20 0.40
MAOB P27338 2/20 0.40
HRH3 Q9Y5N1 1/20 0.40
SLC6A4 P31645 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
Hydrochloric Acid SCHEMBL15671474 0.98 GRIN2D (0.58) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL6997949 0.90 GRIN2D (0.66) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL27484479 0.85 GRIN2D (0.56) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL4310764 0.82 GRIN2D (0.58) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL28580243 0.82 GRIN2D (0.58) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL14860365 0.82 GRIN2D (0.58) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL1269598 0.82 GRIN2D (0.58) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL30819042 0.82 HRH1 (0.54) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL4356380 0.82 HRH1 (0.54) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B
SCHEMBL31758016 0.82 GRIN2D (0.56) GRIN2DGRIN3BGRIN1GRIN2AGRIN2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118019860-A Compositions and methods for detecting analytes 3M创新有限公司 2024-05-10 CN claimed
CN-117425404-A Method for storing MRNA compositions 伊泽阿恩埃免疫疗法股份有限公司 2024-01-19 CN claimed
CN-117045582-A Hydrogel contact lens microneedle capable of transferring medicine and preparation method thereof 金陵科技学院 2023-11-14 CN claimed
US-20230256073-A1 POLYPEPTIDES OF FUSOBACTERIUM AND METHODS OF USE VAXXINOVA US, INC. 2023-08-17 US claimed
CN-116544617-A Lithium ion battery diaphragm 惠州亿纬锂能股份有限公司 2023-08-04 CN claimed
CN-116348502-A Preparation of non-polar block copolymers via vinyl terminated polyolefins 陶氏环球技术有限责任公司 2023-06-27 CN claimed
CN-115385873-B Continuous synthesis method of perfluoro-2, 3-epoxy-2-methylpentane 山东华夏神舟新材料有限公司 2023-01-03 CN claimed
CN-115385873-A Continuous synthesis method of perfluoro-2, 3-epoxy-2-methylpentane 山东华夏神舟新材料有限公司 2022-11-25 CN claimed
CN-113121566-B Pyrene derivative fluorescent molecule and preparation method and application thereof 广东石油化工学院 2022-11-04 CN claimed
CN-112812203-B Initiator and preparation method of polymer/metal oxide composite material 西北工业大学 2022-06-17 CN claimed
EP-2038356-A1 LIQUID HARDENING Unilever PLC (GB) 2009-03-25 EP claimed
CN-101151050-A Agent for control of degranulation reaction and cytokine production RIKEN (JP) 2008-03-26 CN claimed
WO-2008003652-A1 LIQUID HARDENING UNILEVER PLC (GB) 2008-01-10 WO claimed
CN-1913917-A Pharmaceutical composition of thrombin peptide derivatives UNIV TEXAS (US) 2007-02-14 CN claimed
CN-1882340-A Method and composition for treatment or prophylaxis of amyloidosis disorders ACRUX DDS PTY LTD (AU) 2006-12-20 CN claimed
WO-2006081327-A2 SMALL MOLECULES THAT REDUCE FUNGAL GROWTH UNIVERSITY OF VERMONT AND STATE AGRICULTURAL COLLEGE (US) 2006-08-03 WO claimed
EP-0977574-A4 METHODS FOR IN VIVO REDUCTION OF CYANIDE LEVELS AND COMPOSITIONS USEFUL THEREFOR MEDINOX INC (US) 2002-05-22 EP claimed
EP-0977574-A1 METHODS FOR IN VIVO REDUCTION OF CYANIDE LEVELS AND COMPOSITIONS USEFUL THEREFOR Medinox, Inc. (US) 2000-02-09 EP claimed
WO-1999039575-A9 SYNERGISTIC BIOCIDAL ACTIVITY OF TERNARY COMPLEXES OF NEGATIVELY -CHARGED BIOCIDES (COMPONENT A), TRANSITION METAL IONS (COMPONENT B), AND NEUTRAL CHELATORS (COMPONENT C) YISSUM RES DEV CO (IL) 1999-10-21 WO claimed
WO-1998034620-A1 METHODS FOR IN VIVO REDUCTION OF CYANIDE LEVELS AND COMPOSITIONS USEFUL THEREFOR MEDINOX, INC. (US) 1998-08-13 WO claimed