Sulfuric Acid

Sulfuric Acid

SCHEMBL8621246

CCNO.O=S(=O)(O)O

nearest known ligand 0.00

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Known targets — ChEMBL curated mechanism

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

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.

⚠ 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.

Compoundsimilaritytop predictedshared targets
Sulfuric Acid SCHEMBL11350357 1.00 CA5A (0.43)
Sulfuric Acid SCHEMBL28295232 0.88 CA5A (0.33)
Sulfuric Acid SCHEMBL17673102 0.84 MEN1 (0.44)
SCHEMBL4365468 0.82 CA2 (0.33)
SCHEMBL48849 0.80
Trifluoromethanesulfonic Acid SCHEMBL17746594 0.80 CA2 (0.42)
Sulfuric Acid SCHEMBL833022 0.79 CA5A (0.43)
Sulfuric Acid SCHEMBL2389985 0.79
Diethylamine SCHEMBL2064180 0.79 TP53 (0.57)
Diethylamine SCHEMBL2064182 0.79 TP53 (0.57)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114685471-A Preparation method of isoxazoline compound 沈阳科创化学品有限公司 2022-07-01 CN claimed
CN-114685471-B Preparation method of isoxazoline compound 沈阳科创化学品有限公司 2024-02-06 CN disclosed
CN-114685471-A Preparation method of isoxazoline compound 沈阳科创化学品有限公司 2022-07-01 CN disclosed
CN-107266323-B A kind of side chain and its synthetic method, and the method using side chain synthesis hydroxychloroquine sulfate 宜宾莱特医药化工有限公司 2019-04-19 CN disclosed
CN-107266323-A A kind of side chain and its synthetic method, and using the method for side chain synthesis hydroxychloroquine sulfate 宜宾莱特医药化工有限公司 2017-10-20 CN disclosed
CN-103998531-B Three aromatic azo methine direct dyess, dye composite, implementation and the purposes for including at least one such dyestuff 欧莱雅 2017-07-28 CN disclosed
EP-0713139-B1 Novel, iron complex, process for producing the same, photographic processing composition and processing process using the same FUJI PHOTO FILM CO LTD (JP) 1998-06-03 EP disclosed
EP-0713139-A1 Novel, iron complex, process for producing the same, photographic processing composition and processing process using the same FUJI PHOTO FILM CO., LTD. (JP) 1996-05-22 EP disclosed
US-5449592-A Exposure through black and white halftone images from color separation, different spectral distribution of light, yellow and magenta couplers KONICA CORPORATION (JP) 1995-09-12 US disclosed
EP-0387733-B1 Preparation method of amino resin particulate having narrow particle size distribution MITSUI TOATSU CHEMICALS (JP) 1994-11-30 EP disclosed
US-5049645-A Preparation method of amino resin particulate having narrow particle size distribution MITSUI TOATSU CHEMICALS, INC. (JP) 1991-09-17 US disclosed
EP-0387733-A2 Preparation method of amino resin particulate having narrow particle size distribution MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-09-19 EP disclosed
US-4271269-A Regeneration of an enzyme immobilizate DYNAMIT NOBEL AKTIENGESELLSCHAFT (DE) 1981-06-02 US disclosed