Methyl Alcohol

Methyl Alcohol

SCHEMBL6933935

CO.CO.CO.C[Ti](C)(C)(C)(C)C1=CC=CC1

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

⚠ 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
Methyl Alcohol SCHEMBL8040458 1.00
Methyl Alcohol SCHEMBL8419067 1.00
SCHEMBL140408 0.95
Hydrochloric Acid SCHEMBL138586 0.92
Bromide SCHEMBL1539655 0.92
Hydrochloric Acid SCHEMBL3671309 0.92
Hydrochloric Acid SCHEMBL812504 0.92
Fluoride SCHEMBL7642597 0.92
Fluoride SCHEMBL1131129 0.92
Iodide SCHEMBL1539699 0.92

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9105646-B2 Methods for reproducible flash layer deposition INTERMOLECULAR, INC. (US) 2015-08-11 US claimed
US-9012298-B2 Methods for reproducible flash layer deposition INTERMOLECULAR, INC. (US) 2015-04-21 US claimed
US-20140187018-A1 Methods for Reproducible Flash Layer Deposition ELPIDA MEMORY, INC (JP) 2014-07-03 US claimed
US-20140183695-A1 Methods for Reproducible Flash Layer Deposition ELPIDA MEMORY, INC (JP) 2014-07-03 US claimed
US-9105646-B2 Methods for reproducible flash layer deposition INTERMOLECULAR, INC. (US) 2015-08-11 US disclosed
US-9012298-B2 Methods for reproducible flash layer deposition INTERMOLECULAR, INC. (US) 2015-04-21 US disclosed
US-20140187018-A1 Methods for Reproducible Flash Layer Deposition ELPIDA MEMORY, INC (JP) 2014-07-03 US disclosed
US-20140183695-A1 Methods for Reproducible Flash Layer Deposition ELPIDA MEMORY, INC (JP) 2014-07-03 US disclosed
EP-0952994-B1 CATALYST COMPOSITION FOR THE PRODUCTION OF OLEFIN POLYMERS UNIVATION TECH LLC (US) 2003-04-02 EP disclosed
US-6100352-A USING A CATALYST CONSISTING OF A TRANSITION METAL COMPOUND, A COMPOUND CAPABLE OF FORMING AN IONIC COMPOUND BY REACTING WITH THE TRANSITION METAL COMPOUND OR AN OXYGEN-CONTAINING COMPOUND SUCH AS ALUMINOXANE IDEMITSU KOSAN CO., LTD. (JP) 2000-08-08 US disclosed
US-6066703-A Process for the production of olefin polymers UNIVATION TECHNOLOGIES LLC. (US) 2000-05-23 US disclosed
EP-0810238-B1 A process for producing polymer IDEMITSU KOSAN CO (JP) 2000-02-02 EP disclosed
EP-0952994-A1 CATALYST COMPOSITION FOR THE PRODUCTION OF OLEFIN POLYMERS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1999-11-03 EP disclosed
WO-1998030607-A1 CATALYST COMPOSITION FOR THE PRODUCTION OF OLEFIN POLYMERS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1998-07-16 WO disclosed
US-5747406-A CYCLOALKADIENE CATALYSTS WITH TITANIUM, ZIRCONIUM OR HAFNIUM FOR POLYMERIZATION OF OLEFINS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1998-05-05 US disclosed
EP-0810238-A1 A process for producing polymer IDEMITSU KOSAN COMPANY LIMITED (JP) 1997-12-03 EP disclosed
EP-0640090-A1 PROCESS FOR PREPARATION OF MONOCYCLOPENTADIENYL METAL COMPLEX COMPOUNDS AND METHOD OF USE THE DOW CHEMICAL COMPANY (US) 1995-03-01 EP disclosed
WO-1993023412-A1 PROCESS FOR PREPARATION OF MONOCYCLOPENTADIENYL METAL COMPLEX COMPOUNDS AND METHOD OF USE THE DOW CHEMICAL COMPANY (US) 1993-11-25 WO disclosed