Sulfuric Acid

Sulfuric Acid

SCHEMBL28807802

CCN(CC)Cc1ccc(CO)o1.O=S(=O)(O)O

nearest known ligand 0.45

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
ALDH1A1 P00352 6/20 0.45
KDM4E B2RXH2 4/20 0.45
POLB P06746 2/20 0.45
TDP1 Q9NUW8 2/20 0.45
L3MBTL1 Q9Y468 2/20 0.45
GLA P06280 1/20 0.41
HDAC8 Q9BY41 4/20 0.40
HDAC6 Q9UBN7 4/20 0.40
HDAC3 O15379 3/20 0.40
HDAC1 Q13547 3/20 0.40
HDAC2 Q92769 3/20 0.40
HDAC4 P56524 2/20 0.39
HDAC7 Q8WUI4 2/20 0.39
HDAC10 Q969S8 2/20 0.39
HDAC11 Q96DB2 2/20 0.39
HDAC9 Q9UKV0 2/20 0.39
HDAC5 Q9UQL6 2/20 0.39
TSHR P16473 1/20 0.38
LMNA P02545 2/20 0.36
GAA P10253 2/20 0.36

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
SCHEMBL7400838 0.91 ALDH1A1 (0.47) ALDH1A1KDM4EPOLBTDP1L3MBTL1
Iodide SCHEMBL28807797 0.79 POLB (0.54) ALDH1A1KDM4EPOLBTDP1L3MBTL1
SCHEMBL11409042 0.79 ALDH1A1 (0.45) ALDH1A1KDM4EPOLBTDP1L3MBTL1
SCHEMBL29719961 0.79 GLA (0.38) ALDH1A1KDM4EPOLBTDP1L3MBTL1
Hydrochloric Acid SCHEMBL11410866 0.77 ALDH1A1 (0.43) ALDH1A1KDM4EPOLBTDP1HDAC8
SCHEMBL13348016 0.75 POLB (0.47) ALDH1A1KDM4EPOLBTDP1L3MBTL1
Methyl Alcohol SCHEMBL28807801 0.74 GLA (0.37) ALDH1A1KDM4EPOLBTDP1L3MBTL1
SCHEMBL11359610 0.74 ACHE (0.41) ALDH1A1KDM4EPOLBTDP1L3MBTL1
SCHEMBL1733144 0.71 ACHE (0.61) TDP1CYP2C19
SCHEMBL11479635 0.71 ACHE (0.45) ALDH1A1KDM4ETDP1TSHRSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114573530-B Preparation method of biomass alcohol ionic liquid 山东农业大学 2023-07-28 CN disclosed
CN-114573530-A Preparation method of biomass alcohol ionic liquid 山东农业大学 2022-06-03 CN disclosed