Sulfuric Acid

Sulfuric Acid

SCHEMBL2866735

CC[n+]1ccccc1.O=S(=O)([O-])O

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CYP51cyp51Acyp51c

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.36
CHRM2 P08172 2/20 0.35
ADRA2A P08913 2/20 0.35
ADORA3 P0DMS8 2/20 0.35
CHRM1 P11229 2/20 0.35
ACHE P22303 2/20 0.35
SLC6A2 P23975 2/20 0.35
SLC6A4 P31645 2/20 0.35
SLC6A3 Q01959 2/20 0.35
ABCB11 O95342 1/20 0.35
ESR1 P03372 1/20 0.35
PGR P06401 1/20 0.35
HTR1A P08908 1/20 0.35
DRD1 P21728 1/20 0.35
TBXA2R P21731 1/20 0.35
PTGS1 P23219 1/20 0.35
PDE4A P27815 1/20 0.35
ADRA1A P35348 1/20 0.35
OPRM1 P35372 1/20 0.35
DRD3 P35462 1/20 0.35

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
Sulfuric Acid SCHEMBL17102611 0.91 ACHE (0.38) KMT2ACHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL8997505 0.91 KMT2A (0.39) KMT2ACHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL2866733 0.88 ACHE (0.37) KMT2ACHRM2ADRA2AADORA3CHRM1
SCHEMBL5314407 0.88 KMT2A (0.38) KMT2ACHRM2ADRA2AADORA3CHRM1
SCHEMBL1293165 0.88 ACHE (0.37) KMT2ACHRM2ADRA2AADORA3CHRM1
SCHEMBL15941575 0.86 ACHE (0.35) KMT2ACHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL8766842 0.83 ACHE (0.47) KMT2ACHRM2ADRA2AADORA3CHRM1
SCHEMBL3047522 0.83 MAPT (0.37) KMT2ACHRM2ADRA2AADORA3CHRM1
Bicarbonate SCHEMBL10812328 0.81 KMT2A (0.43) KMT2ACHRM2ADRA2AADORA3CHRM1
Bicarbonate SCHEMBL10812331 0.81 KMT2A (0.43) KMT2ACHRM2ADRA2AADORA3CHRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10793749-B2 2-cyanoacrylate-based adhesive composition TOAGOSEI CO., LTD. (JP) 2020-10-06 US disclosed
US-20190233679-A1 2-CYANOACRYLATE-BASED ADHESIVE COMPOSITION TOAGOSEI CO., LTD. (JP) 2019-08-01 US disclosed
EP-3444252-A1 SYNTHESIS OF HETERO IONIC COMPOUNDS USING DIALKYLCARBONATE QUATERNIZATION NantEnergy, Inc. (US) 2019-02-20 EP disclosed
EP-3336962-A1 ELECTROCHEMICAL CELL COMPRISING ELECTROLYTE HAVING HETERO IONIC COMPLEX Fluidic, Inc. (US) 2018-06-20 EP disclosed
US-9793586-B2 Synthesis of hetero compounds using dialkylcarbonate quaternation FLUIDIC, INC. (US) 2017-10-17 US disclosed
EP-2201041-B1 CONVERSION METHOD PETROLIAM NASIONAL BERHAD (PETRONAS) (MY) 2016-12-14 EP disclosed
US-9147919-B2 Methods of producing sulfate salts of cations from heteroatomic compounds and dialkyl sulfates and uses thereof FLUIDIC, INC. (US) 2015-09-29 US disclosed
US-8721795-B2 Conversion method PETROLIAM NASIONAL BERHAD (PETRONAS) (MY) 2014-05-13 US disclosed
US-20110312048-A1 CONVERSION METHOD THE QUEEN'S UNIVERSITY OF BELFAST (GB) 2011-12-22 US disclosed
EP-2201041-A1 CONVERSION METHOD The Queens University of Belfast (GB) 2010-06-30 EP disclosed
EP-1789160-B1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF SE (DE) 2009-11-18 EP disclosed
WO-2009030949-A1 CONVERSION METHOD THE QUEEN'S UNIVERSITY OF BELFAST (GB) 2009-03-12 WO disclosed
EP-2033973-A1 Conversion method The Queen's University of Belfast (GB) 2009-03-11 EP disclosed
EP-1789160-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2007-05-30 EP disclosed
WO-2006029788-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2006-03-23 WO disclosed