Sulfuric Acid

Sulfuric Acid

SCHEMBL11528486

CCCCCCCCSC(=N)N.CCCCCCCCSC(=N)N.O=S(=O)(O)O

nearest known ligand 0.67

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
NOS1 P29475 4/20 0.67
NOS3 P29474 3/20 0.67
NOS2 P35228 3/20 0.67
LMNA P02545 1/20 0.52
HSD17B10 Q99714 1/20 0.48
ALDH1A1 P00352 3/20 0.47
CYP1A2 P05177 5/20 0.47
CYP2C19 P33261 4/20 0.47
HRH4 Q9H3N8 4/20 0.46
TDP1 Q9NUW8 3/20 0.46
HRH2 P25021 1/20 0.46
CYP2D6 P10635 2/20 0.45
BLM P54132 2/20 0.45
KDM4E B2RXH2 1/20 0.45
NPSR1 Q6W5P4 1/20 0.45
CA2 P00918 1/20 0.44
SPHK2 Q9NRA0 1/20 0.42
SPHK1 Q9NYA1 1/20 0.42
EPHX1 P07099 1/20 0.42
TSHR P16473 2/20 0.41

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
SCHEMBL9840999 0.90 NOS1 (0.82) NOS1NOS3NOS2LMNAHSD17B10
SCHEMBL31240346 0.90 NOS1 (0.82) NOS1NOS3NOS2LMNAHSD17B10
SCHEMBL3782640 0.90 NOS1 (0.82) NOS1NOS3NOS2LMNAHSD17B10
SCHEMBL9322246 0.90 NOS1 (0.82) NOS1NOS3NOS2LMNAHSD17B10
SCHEMBL14085945 0.90 NOS1 (0.82) NOS1NOS3NOS2LMNAHSD17B10
SCHEMBL11590702 0.90 NOS1 (0.82) NOS1NOS3NOS2LMNAHSD17B10
Bromide SCHEMBL4732328 0.88 NOS1 (0.78) NOS1NOS3NOS2LMNAHSD17B10
Bromide SCHEMBL9841020 0.88 NOS1 (0.78) NOS1NOS3NOS2LMNAHSD17B10
Hydrochloric Acid SCHEMBL4031599 0.88 NOS1 (0.78) NOS1NOS3NOS2LMNAHSD17B10
Bromide SCHEMBL4785272 0.88 NOS1 (0.78) NOS1NOS3NOS2LMNAHSD17B10

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-4148814-A Process for preparing monohydrocarbyltin trihalides PENNWALT CORPORATION (US) 1979-04-10 US disclosed