Methyl Carbamate

Methyl Carbamate

SCHEMBL8952192

CCO.COC(N)=O

nearest known ligand 0.00

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Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Methyl Carbamate. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

⚠ 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.

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5565603-A REACTING UREA COMPOUND WITH FIRST ALCOHOL TO PRODUCE CARBAMATE COMPOUND, REACTING WITH SECOND ALCOHOL IN PRESENCE OF TIN-CONTAINING CATALYST BADGER LICENSING, LLC 1996-10-15 US disclosed
US-5561094-A USED TO FORM DIALKYL CARBONATE BY REACTING UREA ANDALCOHOLS; FORMING ALKYL CARBAMATE CHEMICAL INTERMEDIATE; REACTING WITH SECON ALCOHOL BADGER LICENSING, LLC 1996-10-01 US disclosed
WO-1995017369-A1 PROCESS FOR MANUFACTURING DIALKYL CARBONATE FROM UREA AND ALCOHOL EXXON CHEMICAL PATENTS INC. (US) 1995-06-29 WO disclosed