SCHEMBL1004010

SCHEMBL1004010

C=C(F)CBr

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
SCHEMBL14511052 0.75
SCHEMBL2545247 0.70
SCHEMBL8174659 0.67
SCHEMBL623454 0.67
SCHEMBL8369464 0.67
SCHEMBL1591041 0.67
SCHEMBL77926 0.67
SCHEMBL10388583 0.67
SCHEMBL20483096 0.67
SCHEMBL3131990 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109504497-B High-temperature anticorrosion repairing agent and preparation method thereof 内蒙古三业科技开发有限公司 2021-07-06 CN claimed
CN-109504497-A A kind of high-temperature anticorrosion renovation agent and preparation method thereof 内蒙古三业科技开发有限公司 2019-03-22 CN claimed
EP-0853634-B1 CONTROL OF MOLECULAR WEIGHT AND END-GROUP FUNCTIONALITY IN POLYMERS COMMW SCIENT IND RES ORG (AU) 2001-12-12 EP claimed
US-6235857-B1 UNSATURATED HALIDE OR SULFONYL CHAIN TRANSFER AGENTS COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 2001-05-22 US claimed
EP-0853634-A4 CONTROL OF MOLECULAR WEIGHT AND END-GROUP FUNCTIONALITY IN POLYMERS COMMW SCIENT IND RES ORG (AU) 1998-09-30 EP claimed
EP-0853634-A1 CONTROL OF MOLECULAR WEIGHT AND END-GROUP FUNCTIONALITY IN POLYMERS COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 1998-07-22 EP claimed
WO-1997013792-A1 CONTROL OF MOLECULAR WEIGHT AND END-GROUP FUNCTIONALITY IN POLYMERS COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 1997-04-17 WO claimed
CN-119923261-A Lysergic acid derivatives with improved LSD-like effect 思维医学股份有限公司 2025-05-02 CN disclosed
US-20250118556-A1 METHOD FOR FORMING DEPOSITION FILM RESONAC CORPORATION (JP) 2025-04-10 US disclosed
CN-116194225-B Composition, substrate with surface layer, method for producing substrate with surface layer, compound, and method for producing compound AGC株式会社 2024-12-24 CN disclosed
EP-4443478-A1 METHOD FOR FORMING DEPOSITION FILM Resonac Corporation (JP) 2024-10-09 EP disclosed
CN-118266061-A Method for forming deposited film 株式会社力森诺科 2024-06-28 CN disclosed
US-20240105466-A1 METHOD FOR FORMING PATTERN OF METAL OXIDE AND METHOD FOR PRODUCING SEMICONDUCTOR ELEMENT RESONAC CORPORATION (JP) 2024-03-28 US disclosed
US-5284855-A Broad-spectrum antibiotics; gramnegative and -positive bacteria, esp. Enterobacter BAYER AKTIENGESELLSCHAFT (DE) 1994-02-08 US disclosed
US-5241076-A 1,4-diazatricyclo [6.3.0.0]undecanes BAYER AKTIENGESELLSCHAFT (DE) 1993-08-31 US disclosed
US-5202337-A Antibacterial agent, feed additive BAYER AKTIENGESELLSCHAFT (DE) 1993-04-13 US disclosed
US-5177210-A Preparation of 2,7-diazabicyclo(3.3.0)octanes BAYER AKTIENGESELLSCHAFT (DE) 1993-01-05 US disclosed
EP-0481274-A1 7-(2,7-Diazabicyclo[3.3.0]octyl)-3-quinolone- and -naphthyridonecarboxylic acid derivatives BAYER AG (DE) 1992-04-22 EP disclosed
US-5071999-A Preparation of 2,7-diazabicyclo[3.3.0]octanes BAYER AKTIENGESELLSCHAFT (DE) 1991-12-10 US disclosed
EP-0393424-A2 Process for the preparation of 2,7-Diazabicyclo(3.3.O)octanes BAYER AG (DE) 1990-10-24 EP disclosed