SCHEMBL7975753

SCHEMBL7975753

CC(C)OC(=O)CI

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL28619359 0.80 LMNA (0.41)
SCHEMBL22557 0.80
SCHEMBL14359573 0.79
SCHEMBL21811503 0.79
SCHEMBL14668161 0.79
SCHEMBL72471 0.77 LMNA (0.62)
SCHEMBL229792 0.77 TSHR (0.50)
SCHEMBL3898613 0.76
SCHEMBL19141781 0.75 MMP1 (0.32)
SCHEMBL18152012 0.74 LMNA (0.48)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210340115-A1 A PROCESS FOR THE PREPARATION OF OZANIMOD AND ITS INTERMEDIATE (S)-l-AMINO-2,3-DIHYDRO-1H-INDENE-4-CARBONITRILE PHARMAZELL GMBH (DE) 2021-11-04 US claimed
EP-3849965-A1 A PROCESS FOR THE PREPARATION OF OZANIMOD AND ITS INTERMEDIATE (S)-1-AMINO-2,3-DIHYDRO-1H-INDENE-4-CARBONITRILE Pharmazell GmbH (DE) 2021-07-21 EP claimed
CN-112771028-A Process for the preparation of azamod and its intermediate (S) -1-amino-2, 3-dihydro-1H-indenyl-4-carbonitrile 细胞制药有限公司 2021-05-07 CN claimed
WO-2020053334-A1 A PROCESS FOR THE PREPARATION OF OZANIMOD AND ITS INTERMEDIATE (S)-1-AMINO-2,3-DIHYDRO-1H-INDENE-4-CARBONITRILE PHARMAZELL GMBH (DE) 2020-03-19 WO claimed
US-20250011480-A1 CURABLE RESIN COMPOSITION KYOEISHA CHEMICAL CO., LTD. (JP) 2025-01-09 US disclosed
EP-4414426-A1 CURABLE RESIN COMPOSITION Kyoeisha Chemical Co., Ltd. (JP) 2024-08-14 EP disclosed
CN-118019808-A Curable resin composition 共荣社化学株式会社 2024-05-10 CN disclosed
US-11958802-B2 Migration-resistant photopolymerization sensitizer KAWASAKI KASEI CHEMICALS LTD. (JP) 2024-04-16 US disclosed
CN-113166036-B Photopolymerizing sensitizers with migration resistance 川崎化成工业株式会社 2023-10-10 CN disclosed
WO-2023080228-A1 CURABLE RESIN COMPOSITION 共栄社化学株式会社 2023-05-11 WO disclosed
US-20230110863-A1 THERMOSETTING RESIN COMPOSITION AND TRANSESTERIFICATION REACTION CATALYST KYOEISHA CHEMICAL CO., LTD. (JP) 2023-04-13 US disclosed
EP-4098696-A1 THERMOSETTING RESIN COMPOSITION AND TRANSESTERIFICATION REACTION CATALYST Kyoeisha Chemical Co., Ltd. (JP) 2022-12-07 EP disclosed
WO-2020053334-A1 A PROCESS FOR THE PREPARATION OF OZANIMOD AND ITS INTERMEDIATE (S)-1-AMINO-2,3-DIHYDRO-1H-INDENE-4-CARBONITRILE PHARMAZELL GMBH (DE) 2020-03-19 WO disclosed
CN-110536885-A Method for producing difluoromethylene compound SATO PHARMA 2019-12-03 CN disclosed
WO-2013091502-A1 TRI-HETEROCYCLIC DERIVATIVES, PREPARATION PROCESS AND USES THEREOF SHANGHAI DE NOVO PHARMATECH CO LTD. (CN) 2013-06-27 WO disclosed
CN-1328278-C N-acylamino acid amide compounds and intermediates for preparation thereof UBE INDUSTRIES (JP) 2007-07-25 CN disclosed
US-20070093523-A1 Tetrahydroisoquinoline LXR modulators BRISTOL-MYERS SQUIBB COMPANY 2007-04-26 US disclosed
US-6265418-B1 ANTICOAGULANTS UBE INDUSTRIES, LTD. (JP) 2001-07-24 US disclosed
CN-1265661-A N-acylamino acid amide compounds and intermediates for preparation thereof UBE INDUSTRIES (JP) 2000-09-06 CN disclosed
EP-1020467-A1 N-ACYLAMINO ACID AMIDE COMPOUNDS AND INTERMEDIATES FOR PREPARATION THEREOF UBE INDUSTRIES LIMITED (JP) 2000-07-19 EP disclosed