Sulfuric Acid

Sulfuric Acid

SCHEMBL6233490

CC(F)(F)F.O=S(=O)(O)O

nearest known ligand 0.50

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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.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA5A P35218 2/20 0.50
CA5B Q9Y2D0 2/20 0.50
TSHR P16473 3/20 0.43
TDP1 Q9NUW8 1/20 0.43
ALDH1A1 P00352 2/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
CA1 P00915 3/20 0.35
CA2 P00918 3/20 0.35
CA7 P43166 2/20 0.35
CA13 Q8N1Q1 1/20 0.35
KDM4E B2RXH2 2/20 0.33
BLM P54132 2/20 0.33
NT5E P21589 1/20 0.33
CA4 P22748 1/20 0.33
CA6 P23280 1/20 0.33
CA9 Q16790 1/20 0.33
CYP2D6 P10635 1/20 0.33
CYP2C19 P33261 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
MEN1 O00255 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
Hydrochloric Acid SCHEMBL27963455 0.85 CA2 (0.39) CA5ACA5BTSHRTDP1ALDH1A1
Trifluoromethanesulfonic Acid SCHEMBL336431 0.85 ALDH1A1 (0.43) CA5ACA5BTSHRTDP1ALDH1A1
SCHEMBL9050706 0.85 TSHR (0.38) CA5ACA5BTSHRTDP1ALDH1A1
Sulfuric Acid SCHEMBL4353784 0.82 CA5A (0.60) CA5ACA5BTSHRTDP1ALDH1A1
Sulfuric Acid SCHEMBL11313030 0.82 CA5A (0.60) CA5ACA5BTSHRTDP1ALDH1A1
Sulfuric Acid SCHEMBL9744014 0.82 CA5A (0.60) CA5ACA5BTSHRTDP1ALDH1A1
SCHEMBL575399 0.80
SCHEMBL1398392 0.80
SCHEMBL29156137 0.79 TSHR (0.50) TSHRTDP1ALDH1A1L3MBTL1CA2
SCHEMBL28449124 0.78 CA1 (0.38) TSHRTDP1CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112334497-A Radiopaque polymers 生物相容英国有限公司 2021-02-05 CN disclosed
CN-101698644-B Method for efficiently preparing trifluroethyl vinyl ether without solvent DONGYUE SHENZHOU NEW MAT CO 2010-12-29 CN disclosed
CN-101698654-B Method for preparing functional fluorine-containing monomers by bulk catalysis DONGYUE SHENZHOU NEW MAT CO 2010-11-10 CN disclosed
CN-101698654-A Method for preparing functional fluorine-containing monomers by bulk catalysis DONGYUE SHENZHOU NEW MAT CO 2010-04-28 CN disclosed
CN-101698644-A Method for efficiently preparing trifluroethyl vinyl ether without solvent DONGYUE SHENZHOU NEW MAT CO 2010-04-28 CN disclosed
CN-101698635-A Preparation method of alkyl ether with ether terminal group DONGYUE SHENZHOU NEW MAT CO 2010-04-28 CN disclosed
US-20050010044-A1 Polysaccharides and methods and intermediates useful for their preparation NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2005-01-13 US disclosed
WO-2005000907-A1 SULFO-PROTECTED POLYSACCHARIDES AND METHODS AND INTERMEDIATES USEFUL FOR THEIR PREPARATION UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2005-01-06 WO disclosed
EP-0548616-A1 Aqueous chemiluminescent systems AMERICAN CYANAMID COMPANY (US) 1993-06-30 EP disclosed