Sulfuric Acid

Sulfuric Acid

SCHEMBL11650367

CN(C)CCBr.O=S(=O)(O)O

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

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
CHRM2 known ✓ P08172 1/20 0.31
CHRM1 known ✓ P11229 1/20 0.31
CHRM3 known ✓ P20309 1/20 0.31
ALDH1A1 P00352 2/20 0.41
MAPT P10636 1/20 0.36
CA5A P35218 2/20 0.33
CA5B Q9Y2D0 2/20 0.33
NPSR1 Q6W5P4 2/20 0.32
TSHR P16473 2/20 0.32
TDP1 Q9NUW8 1/20 0.32
CA12 O43570 1/20 0.32
CA2 P00918 1/20 0.32
CA3 P07451 1/20 0.32
CA4 P22748 1/20 0.32
CA6 P23280 1/20 0.32
CA7 P43166 1/20 0.32
CA9 Q16790 1/20 0.32
CA14 Q9ULX7 1/20 0.32
CHRM4 P08173 1/20 0.31
CHRM5 P08912 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 SCHEMBL28411524 0.82 CA5A (0.47) ALDH1A1MAPTCA5ACA5BNPSR1
SCHEMBL7565 0.82
Sulfuric Acid SCHEMBL27808254 0.79 CA5A (0.44) ALDH1A1MAPTCA5ACA5BNPSR1
Bromide SCHEMBL28116 0.78
Hydrochloric Acid SCHEMBL659254 0.78
Dimethylaminoethanol SCHEMBL1131844 0.74 MAPT (0.71) ALDH1A1MAPTCA5ACA5BTSHR
Dimethylaminoethanol SCHEMBL1131385 0.74 MAPT (0.71) ALDH1A1MAPTCA5ACA5BTSHR
Sulfuric Acid SCHEMBL27714292 0.74 CA1 (0.46) ALDH1A1MAPTCA5ACA5BNPSR1
Sulfuric Acid SCHEMBL11647815 0.72 MAPT (0.43) ALDH1A1MAPTCA5ACA5BNPSR1
SCHEMBL29988628 0.72 MAPT (0.36) ALDH1A1MAPTCA5ACA5BTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4104307-A BY REACTING DRY HYDROGEN HALIDE AND 2-AMINOALKYL MONOSULFATE ESTERS NATIONAL STARCH AND CHEMICAL CORPORATION (US) 1978-08-01 US claimed