Sulfuric Acid

Sulfuric Acid

SCHEMBL7108309

CC[N+](C)(CC)CC.O=S(=O)([O-])O

nearest known ligand 0.44

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 5)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.44
ALDH1A1 P00352 1/20 0.44
TSHR P16473 1/20 0.44
KMT2A Q03164 1/20 0.44
BBOX1 O75936 5/20 0.39

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 SCHEMBL7641807 0.88 BBOX1 (0.42) BBOX1
Sulfuric Acid SCHEMBL17102659 0.88 CA5A (0.40) BBOX1
Sulfuric Acid SCHEMBL7108307 0.85 BBOX1 (0.41) BBOX1
SCHEMBL4657818 0.85 BBOX1 (0.41) BBOX1
SCHEMBL4886484 0.85 BBOX1 (0.36) MEN1KMT2ABBOX1
Sulfuric Acid SCHEMBL3467201 0.85 TSHR (0.47) MEN1ALDH1A1TSHRKMT2ABBOX1
Sulfuric Acid SCHEMBL18008312 0.82 BBOX1 (0.50) MEN1ALDH1A1TSHRKMT2ABBOX1
Sulfuric Acid SCHEMBL28984262 0.82 MEN1 (0.44) MEN1ALDH1A1TSHRKMT2ABBOX1
Tetrylammonium SCHEMBL36705 0.79 TSHR (0.50) MEN1ALDH1A1TSHRKMT2ABBOX1
Sulfuric Acid SCHEMBL7543978 0.78 MEN1 (0.40) MEN1ALDH1A1TSHRKMT2ABBOX1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105826596-B Preparation method of ionic liquid and secondary battery 微宏动力系统(湖州)有限公司 2020-11-06 CN disclosed
US-10312551-B2 Preparation method of ionic liquids and secondary batteries MICROVAST POWER SYSTEMS CO., LTD. (CN) 2019-06-04 US disclosed
US-20170077557-A1 THE PREPARATION METHOD OF IONIC LIQUID AND THE SECONDARY BATTERY MICROVAST POWER SYSTEMS CO., LTD. (CN) 2017-03-16 US 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
CN-1635992-A Solventless synthesis of hydrophilic phenol ester derivatives PROCTER & GAMBLE (US) 2005-07-06 CN disclosed
EP-1351927-A2 SOLVENTLESS SYNTHESIS OF HYDROPHILIC PHENOL ESTER DERIVATIVES THE PROCTER & GAMBLE COMPANY (US) 2003-10-15 EP disclosed
WO-2002040447-A2 SOLVENTLESS SYNTHESIS OF HYDROPHILIC PHENOL ESTER DERIVATIVES THE PROCTER & GAMBLE COMPANY (US) 2002-05-23 WO disclosed
US-20020058824-A1 Solventless synthesis of hydrophilic phenol ester derivatives PROCTER & GAMBLE COMPANY, THE 2002-05-16 US disclosed
EP-0579738-B1 IMPROVED PROCESS FOR PREPARING PHENYL ESTERS OF SUBSTITUTED ACIDS DU PONT (US) 1996-08-28 EP disclosed
EP-0577746-B1 IMPROVED PROCESS FOR PREPARING PHENYL CHLOROACETATE DU PONT (US) 1996-02-28 EP disclosed
EP-0579738-A1 IMPROVED PROCESS FOR PREPARING PHENYL ESTERS OF SUBSTITUTED ACIDS. DU PONT (US) 1994-01-26 EP disclosed
EP-0577746-A1 IMPROVED PROCESS FOR PREPARING PHENYL CHLOROACETATE. DU PONT (US) 1994-01-12 EP disclosed
US-5235077-A PROCESS FOR PREPARING PHENYL ESTERS OF SUBSTITUTED ACIDS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1993-08-10 US disclosed
WO-1992016492-A1 IMPROVED PROCESS FOR PREPARING PHENYL ESTERS OF SUBSTITUTED ACIDS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1992-10-01 WO disclosed
WO-1992016491-A1 IMPROVED PROCESS FOR PREPARING PHENYL CHLOROACETATE E.I. DU PONT DE NEMOURS AND COMPANY (US) 1992-10-01 WO disclosed
US-5069828-A PROCESS FOR PREPARING BENZENESULFONATE SALTS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1991-12-03 US disclosed
US-4985180-A Process for preparing phenyl esters of substituted acids E. I. DU PONT DE NEMOURS AND COMPANY (US) 1991-01-15 US disclosed
EP-0402048-A1 Improved process for preparing benzenesulfonate salts E.I. DU PONT DE NEMOURS AND COMPANY (US) 1990-12-12 EP disclosed
EP-0402047-A1 Improved process for preparing phenyl esters of substituted acids E.I. DU PONT DE NEMOURS AND COMPANY (US) 1990-12-12 EP 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 (1 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-20020058824-A1 Solventless synthesis of hydrophilic phenol ester derivatives MPHOSPH6, HACL2, PHKB MEN1 4088/4885ALDH1A1 4568/4885TSHR 4127/4885

“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.