SCHEMBL6239009

SCHEMBL6239009

CNCC(C)CNC

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
SCHEMBL6274547 0.85 KISS1R (0.33)
SCHEMBL13020901 0.82
SCHEMBL178422 0.82
SCHEMBL27105034 0.82
SCHEMBL12040160 0.82
Hydrochloric Acid SCHEMBL25280389 0.79
SCHEMBL24534361 0.79
SCHEMBL15934167 0.79
Hydrochloric Acid SCHEMBL25280388 0.79
SCHEMBL21729964 0.79

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9908953-B2 Crosslinker-accelerator system for polyacrylates TESA SE (DE) 2018-03-06 US claimed
EP-2617789-B1 Crosslinking accelerator system for polyacrylates TESA SE (DE) 2014-12-17 EP claimed
WO-2024073371-A1 AKT1 MODULATORS ALTEROME THERAPEUTICS, INC. (US) 2024-04-04 WO disclosed
WO-2024064026-A1 AKT1 MODULATORS ALTEROME THERAPEUTICS, INC. (US) 2024-03-28 WO disclosed
EP-4119126-A1 NANOFORMULATION WITH DIVERSE FUNCTIONAL MOLECULES FROM TURMERIC AND PROCESS FOR PREPARATION OF THE SAME Zeroharm Sciences Private Limited (IN) 2023-01-18 EP disclosed
US-11359115-B2 Adhesive system made of a multiplicity of pressure-sensitive adhesive layers TESA SE (DE) 2022-06-14 US disclosed
EP-3538596-B1 ADHESIVE KIT OF SEVERAL PRESSURE SENSITIVE ADHESIVE LAYERS TESA SE (DE) 2021-01-20 EP disclosed
US-20190284446-A1 ADHESIVE SYSTEM MADE OF A MULTIPLICITY OF PRESSURE-SENSITVE ADHESIVE LAYERS TESA SE (DE) 2019-09-19 US disclosed
US-9908953-B2 Crosslinker-accelerator system for polyacrylates TESA SE (DE) 2018-03-06 US disclosed
US-20170312363-A1 MULTIFUNCTIONALIZED POLYETHYLENE GLYCOL DERIVATIVE AND PREPARATION METHOD THEREFOR XIAMEN SINOPEG BIOTECH CO., LTD. (CN) 2017-11-02 US disclosed
US-20170158647-A1 MODULATORS OF PHARMACOKINETIC PROPERTIES OF THERAPEUTICS GILEAD SCIENCES, INC. 2017-06-08 US disclosed
US-6136984-A Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes NOVO NORDISK A/S (DK) 2000-10-24 US disclosed
US-5847150-A Solid phase and combinatorial synthesis of substituted 2-methylene-2, 3-dihydrothiazoles and of arrays of substituted 2-methylene-2, 3-dihydrothiazoles NOVO NORDISK A/S (DK) 1998-12-08 US disclosed
WO-1997040025-A1 SOLID PHASE AND COMBINATORIAL SYNTHESIS OF SUBSTITUTED 1,2,3-TRIAZOLES AND OF ARRAYS OF SUBSTITUTED 1,2,3-TRIAZOLES NOVO NORDISK A/S (DK) 1997-10-30 WO disclosed
EP-0590419-A1 Process for preparing unsaturated amines BASF Aktiengesellschaft (DE) 1994-04-06 EP disclosed
US-4900820-A REACTING UREA WITH ACYCLIC DIAMINE MITSUI TOATSU CHEMICALS, INC. (JP) 1990-02-13 US disclosed
US-4788277-A OXIDATIVE COUPLING, CATALYST CONTAINING COPPER, DIAMINE, HALOGEN ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1988-11-29 US disclosed
EP-0249136-A2 Process for producing cyclic ureas MITSUI TOATSU CHEMICALS, Inc. (JP) 1987-12-16 EP disclosed
US-4189306-A OCTANE RATING IMPROVERS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1980-02-19 US disclosed
US-4180386-A ANTIKNOCK FUEL ADDITIVES E. I. DU PONT DE NEMOURS & COMPANY (US) 1979-12-25 US disclosed