Sulfuric Acid

Sulfuric Acid

SCHEMBL898121

O=S(=O)([O-])[O-].O=S(=O)([O-])[O-].O=S(=O)([O-])[O-].[Fe+2].[Fe+2].[NH4+].[NH4+]

nearest known ligand 0.42

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

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 5)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.42
ALDH1A1 P00352 1/20 0.42
TSHR P16473 1/20 0.42
KMT2A Q03164 1/20 0.42
TP53 P04637 1/20 0.38

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 SCHEMBL29992414 1.00
Sulfuric Acid SCHEMBL65556 1.00 MEN1 (0.42) MEN1ALDH1A1TSHRKMT2ATP53
Sulfuric Acid SCHEMBL31172741 0.94
Sulfuric Acid SCHEMBL32662881 0.94 MEN1 (0.39) MEN1ALDH1A1TSHRKMT2ATP53
Sulfuric Acid SCHEMBL9679294 0.94 MEN1 (0.39) MEN1ALDH1A1TSHRKMT2ATP53
Sulfuric Acid SCHEMBL2031104 0.94 MEN1 (0.39) MEN1ALDH1A1TSHRKMT2ATP53
Sulfuric Acid SCHEMBL4243306 0.94 MEN1 (0.39) MEN1ALDH1A1TSHRKMT2ATP53
Sulfuric Acid SCHEMBL15416683 0.94
Sulfuric Acid SCHEMBL10887661 0.94 ALDH1A1 (0.50) MEN1ALDH1A1TSHRKMT2ATP53
Sulfuric Acid SCHEMBL19138778 0.94

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130109563-A1 PREPARING CERIUM(III) COMPOUNDS BASF SE (DE) 2013-05-02 US claimed
US-7691934-B2 High molecular weight poly(dially dialkyl) ammonium salts CIBA SPECIALTY CHEMICALS CORPORATION (US) 2010-04-06 US claimed
US-20070093626-A1 High molecular weight poly(dially dialkyl) ammonium salts CIBA SPECIALTY CHEMICALS CORP. 2007-04-26 US claimed
US-20150257383-A1 METHOD FOR COMBATING PHYTOPATHOGENIC HARMFUL MICROBES ON CULTIVATED PLANTS OR PLANT PROPAGATION MATERIAL BASF SE (DE) 2015-09-17 US disclosed
US-8821910-B2 Alkylaminoalkyl oligomers as broad-spectrum antimicrobial agent BASF SE (DE) 2014-09-02 US disclosed
US-20140170238-A1 Antimicrobial effects in polymers BASF SE (DE) 2014-06-19 US disclosed
US-20130109563-A1 PREPARING CERIUM(III) COMPOUNDS BASF SE (DE) 2013-05-02 US disclosed
US-20130095719-A1 Mineral Wool Fiber Mats, Method for Producing Same, and Use CELANESE EMULSIONS GMBH (DE) 2013-04-18 US disclosed
US-20120330209-A1 Non-leaching Antimicrobial Wound Dressing SONG ZHIQIANG (US) 2012-12-27 US disclosed
US-20120328683-A1 Alkylaminoalkyl oligomers as broad-spectrum antimicrobial agent SONG ZHIQIANG (US) 2012-12-27 US disclosed
US-8173757-B2 Process for production of polymer powders containing vinylformamide units BASF AKTIENGESELLSCHAFT (DE) 2012-05-08 US disclosed
EP-0359509-B1 Process for the production of high molecular weight copolymers of diallyl dimethyl ammonium chloride and acrylamide in solution DOW CHEMICAL CO (US) 1994-01-26 EP disclosed
US-5200482-A Prepared with chain transfer agent to prevent branching and crosslinking; flocculants in waste water treatment THE DOW CHEMICAL COMPANY (US) 1993-04-06 US disclosed
US-5185411-A POLYMERIZATION OF WATER-SOLUBLE MONOMERS THE DOW CHEMICAL COMPANY (US) 1993-02-09 US disclosed
EP-0495312-A1 Polymerization of water soluble monomers THE DOW CHEMICAL COMPANY (US) 1992-07-22 EP disclosed
EP-0363024-A1 Process for the production of high molecular weight copolymers of diallyl dimethyl ammonium chloride and acrylamide in an aqueous dispersed phase THE DOW CHEMICAL COMPANY (US) 1990-04-11 EP disclosed
EP-0359509-A1 Process for the production of high molecular weight copolymers of diallyl dimethyl ammonium chloride and acrylamide in solution THE DOW CHEMICAL COMPANY (US) 1990-03-21 EP disclosed
US-4125401-A Method of making copies of information tracks on carriers U.S. PHILIPS CORPORATION (US) 1978-11-14 US disclosed
US-4118556-A Process for the production of acrylonitrile-vinyl-chloride copolymers with improved whiteness BAYER AKTIENGESELLSCHAFT (DE) 1978-10-03 US disclosed
US-4100339-A Process for preparing acrylonitrile/vinyl chloride copolymers having an increased viscosity which comprises using anionic/non-ionic emulsifier blends BAYER AKTIENGESELLSCHAFT (DE) 1978-07-11 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20150257383-A1 METHOD FOR COMBATING PHYTOPATHOGENIC HARMFUL MICROBES ON CULTIVATED PLANTS OR PLANT PROPAGATION MATERIAL AHCY, AGPS, AS3MT MEN1 2350/4885ALDH1A1 2603/4885TSHR 3846/4885
US-20120328683-A1 Alkylaminoalkyl oligomers as broad-spectrum antimicrobial agent CUTA, AAAS, NACA MEN1 1908/4885ALDH1A1 1560/4885TSHR 4343/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.