Carbamic Acid

Carbamic Acid

SCHEMBL5435002

NC(=O)O.O=NO

nearest known ligand 0.00

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⚠ 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
Urea SCHEMBL8835038 0.86
Nitrous Acid SCHEMBL14844130 0.82 CA2 (0.55)
Urea SCHEMBL28471496 0.82
Bicarbonate SCHEMBL6033140 0.80
Bicarbonate SCHEMBL9637401 0.80 CA1 (0.67)
Carbamic Acid SCHEMBL2564971 0.80 ACHE (1.00)
Carbamic Acid SCHEMBL5048206 0.80 ACHE (1.00)
Carbamic Acid SCHEMBL8512703 0.80 ACHE (1.00)
Carbamic Acid SCHEMBL4466151 0.80 ACHE (1.00)
Nitrous Acid SCHEMBL2348981 0.80

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030125507-A1 Polyamide BASF AKTIENGESELLSCHAFT (DE) 2003-07-03 US claimed
CN-110461336-A Drug-polymer conjugate POLYACTIVA PTY LTD 2019-11-15 CN disclosed
US-8268955-B2 Polyamides BASF SE (DE) 2012-09-18 US disclosed
US-7285601-B2 Fibers, films, and moldings; monoolefinically unsaturated monocarboxylic acid of the formula CH2 .dbd. CH (CH2)3 COOH chemically bonded at the end of the polymer chain via an amide group BASF AKTIENGESELLSCHAFT (DE) 2007-10-23 US disclosed
US-20060063907-A1 Polyamides BASF AKTIENGESELLSCHAFT (DE) 2006-03-23 US disclosed
US-20050159579-A1 Inherently crosslinkable polyamides BASF AKTIENGESELLSCHAFT (DE) 2005-07-21 US disclosed
US-6812322-B2 POLYMERIZED IN PRESENCE OF STERICALLY HINDERED 4-AMINO-2,2,6,6-TETRAMETHYLPIPERIDINE; FIBERS, SHEETS AND MOLDINGS BASF AKTIENGESELLSCHAFT (DE) 2004-11-02 US disclosed
US-6774205-B2 CONDENSATION POLYMERIZATION AND AMIDATION OF LACTAMS, AMINOCARBOXYLIC ACIDS AND DERIVATIVES; DICARBOXYLIC ACIDS AND DIAMINES, AND SULFODICARBOXYLIC ACIDS IN PRESENCE OF STERICALLY HINDERED PIPERIDINE BASF AKTIENGESELLSCHAFT (DE) 2004-08-10 US disclosed
US-6686465-B2 GAS PHASE REACTION 6-AMINOCAPRONITRILE WITH STEAM IN PRESENCE OF HETEROGENEOUS CYCLIZATION CATALYST, ADDING DILUENT TO CREATE MISCIBILITY GAP WITH WATER, THEN SEPARATING HIGH-/LOW-BOILING BASF AKTIENGESELLSCHAFT (DE) 2004-02-03 US disclosed
US-20030135017-A1 From amide monomers including a sterically hindered piperidine derivative with a functional group capable of amide formation and a sulfonated compound with 2 or more carboxyl groups or derivatives BASF AKTIENGESELLSCHAFT (DE) 2003-07-17 US disclosed
US-20030125507-A1 Polyamide BASF AKTIENGESELLSCHAFT (DE) 2003-07-03 US disclosed
US-20030125544-A1 Method for producing cyclic lactams BASF AKTIENGESELLSCHAFT (DE) 2003-07-03 US disclosed