Carbamic Acid

Carbamic Acid

SCHEMBL173704

NC(=O)O.O

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Carbamic Acid. 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 251 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108350336-A Adhesive composition for optical applications 株式会社LG化学 2018-07-31 CN claimed
WO-2017002131-A1 CRYSTALLINE FORMS OF N-(2-CHLORO-6-METHY]PHENVN-2-[F6-[4-(2-HVDROXVETHVL)-L- PIPERAZINVIL-2-METHVL-4-PVRIMIDINVLLAMINOL-5-THIAZOLECARBOXAMIDE AND THEIR PROCESS THEREOF MSN LABORATORIES PRIVATE LIMITED (IN) 2017-01-05 WO claimed
CN-102712579-B Method for producing isocyanates by thermally cracking carbamates BASF SE 2014-07-09 CN claimed
CN-103228693-A Polyurethane-based coating for display areas SCHOTT AG 2013-07-31 CN claimed
EP-2564831-A1 Dermatological emulsion and method for preparing same Pierre Fabre Dermo-Cosmétique (FR) 2013-03-06 EP claimed
WO-2010030835-A2 PHARMACEUTICAL COMPOSITIONS OF AN SRC KINASE INHIBITOR AND AN AROMATASE INHIBITOR WYETH LLC (US) 2010-03-18 WO claimed
EP-2114373-A1 DERMATOLOGICAL EMULSION AND METHOD FOR THE PREPARATION THEREOF Pierre Fabre Dermo-Cosmetique (FR) 2009-11-11 EP claimed
WO-2008095796-A1 DERMATOLOGICAL EMULSION AND METHOD FOR THE PREPARATION THEREOF PIERRE FABRE DERMO-COSMETIQUE (FR) 2008-08-14 WO claimed
EP-1556454-A1 COMPOUNDS HAVING A SECONDARY OR TERTIARY HYDROXY OR HALIDE GROUP SEPARATED FROM A PRIMARY CARBAMATE GROUP BY THREE OR MORE CARBON ATOMS AND A METHOD OF MAKING THE SAME Basf Corporation (US) 2005-07-27 EP claimed
WO-2004041948-A1 COMPOUNDS HAVING A SECONDARY OR TERTIARY HYDROXY OR HALIDE GROUP SEPARATED FROM A PRIMARY CARBAMATE GROUP BY THREE OR MORE CARBON ATOMS AND A METHOD OF MAKING THE SAME BASF CORPORATION (US) 2004-05-21 WO claimed
US-20040087738-A1 Compounds having a secondary or tertiary hydroxy or halide group separated from a primary carbamate group by three or more carbon atoms and a method of making the same BASF CORPORATION 2004-05-06 US claimed
JP-52136127-A None JP disclosed
CN-119630634-A Method for preparing modulators of eukaryotic initiation factor 2B 戴纳立制药公司 2025-03-14 CN disclosed
CN-118620556-A Acrylic ester pressure-sensitive adhesive and preparation method and application thereof 昆山石梅新材料科技有限公司 2024-09-10 CN disclosed
US-20240218288-A1 EFFICIENT SURFACTANT SYSTEM ON PLASTIC AND ALL TYPES OF WARE BASF SE (DE) 2024-07-04 US disclosed
WO-1996030473-A1 REDUCED RESIDUE HARD SURFACE CLEANER THE CLOROX COMPANY (US) 1996-10-03 WO disclosed
US-4567294-A Preparation of ammonium carbamate BASF AKTIENGESELLSCHAFT (DE) 1986-01-28 US disclosed
US-4204858-A POST EMERGENCE HERBICIDES FOR RICE STAUFFER CHEMICAL COMPANY (US) 1980-05-27 US disclosed
US-4169152-A Isohexide and tetrahydrofuran ethers and their carbamates in method of bringing about relaxation of skeletal musculature ICI AMERICAS INC. (US) 1979-09-25 US disclosed
JP-S52136127-A PROCESS FOR MANUFACTURING MIXTURES FROM PENTAERYTHROTCARBAMATE* POLYALKYLENEGLYCOL ETHER CARBAMATE AND ALKYLALKYLENEGLYCOL CARBAMATE BASF AG 1977-11-14 JP disclosed