Sulfuric Acid

Sulfuric Acid

SCHEMBL7543978

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

nearest known ligand 0.40

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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 10)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
ALDH1A1 P00352 1/20 0.40
TSHR P16473 1/20 0.40
BBOX1 O75936 5/20 0.37
SLC22A1 O15245 1/20 0.32
LMNA P02545 1/20 0.31
POLB P06746 1/20 0.31
GRK2 P25098 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31

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 SCHEMBL8397794 0.89 BBOX1 (0.39) TSHRBBOX1SLC22A1
Sulfuric Acid SCHEMBL7543975 0.86 BBOX1 (0.38) BBOX1SLC22A1
Tributylmethylammonium SCHEMBL268725 0.85 MEN1 (0.39) MEN1KMT2AALDH1A1TSHRBBOX1
Sulfuric Acid SCHEMBL15361710 0.84 BBOX1 (0.46) MEN1KMT2AALDH1A1TSHRBBOX1
Sulfuric Acid SCHEMBL6405441 0.81 LSS (0.48) KMT2ASLC22A1
Sulfuric Acid SCHEMBL781963 0.81 LSS (0.48) KMT2ASLC22A1
Sulfuric Acid SCHEMBL6257863 0.81 LSS (0.48) KMT2ASLC22A1
Sulfuric Acid SCHEMBL2544115 0.81 LSS (0.48) KMT2ASLC22A1
Sulfuric Acid SCHEMBL6054968 0.81 LSS (0.48) KMT2ASLC22A1
Sulfuric Acid SCHEMBL6261099 0.81 LSS (0.48) KMT2ASLC22A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1635992-A Solventless synthesis of hydrophilic phenol ester derivatives PROCTER & GAMBLE (US) 2005-07-06 CN disclosed
US-20020058824-A1 Solventless synthesis of hydrophilic phenol ester derivatives PROCTER & GAMBLE COMPANY, THE 2002-05-16 US disclosed
EP-0577746-B1 IMPROVED PROCESS FOR PREPARING PHENYL CHLOROACETATE DU PONT (US) 1996-02-28 EP disclosed
EP-0577746-A1 IMPROVED PROCESS FOR PREPARING PHENYL CHLOROACETATE. DU PONT (US) 1994-01-12 EP 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

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 4088/4885KMT2A 1638/4885ALDH1A1 4568/4885

“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.