Sulfuric Acid

Sulfuric Acid

SCHEMBL7067929

CNCCCN(C)C.O=S(=O)(O)O

nearest known ligand 0.50

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
PRMT3 O60678 1/20 0.50
CARM1 Q86X55 1/20 0.50
PRMT6 Q96LA8 1/20 0.50
PRMT1 Q99873 1/20 0.50
PRMT8 Q9NR22 1/20 0.50
PAOX Q6QHF9 1/20 0.46
CA12 O43570 1/20 0.41
CA2 P00918 1/20 0.41
CA9 Q16790 1/20 0.41
ALDH1A1 P00352 3/20 0.40
TDP1 Q9NUW8 1/20 0.40
ALOX15 P16050 1/20 0.40
DNM1 Q05193 1/20 0.39
KDM4A O75164 1/20 0.38
KDM4C Q9H3R0 1/20 0.38
TSHR P16473 1/20 0.38
EPHX1 P07099 1/20 0.37
KMT2A Q03164 1/20 0.37
MAPT P10636 1/20 0.36
KDM4E B2RXH2 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
SCHEMBL48440 0.85
SCHEMBL380653 0.83
SCHEMBL27173945 0.83 PRMT3 (0.63) PRMT3CARM1PRMT6PRMT1PRMT8
Ammonia Solution, Strong SCHEMBL19410297 0.83
Hydrochloric Acid SCHEMBL7289584 0.83 PRMT3 (0.63) PRMT3CARM1PRMT6PRMT1PRMT8
Alcohol SCHEMBL28731571 0.81 PRMT3 (0.55) PRMT3CARM1PRMT6PRMT1PRMT8
SCHEMBL25212094 0.80 ALDH1A1 (0.61) PRMT3CARM1PRMT6PRMT1PRMT8
SCHEMBL34673 0.80 ALDH1A1 (0.61) PRMT3CARM1PRMT6PRMT1PRMT8
SCHEMBL1408747 0.80 ALDH1A1 (0.61) PRMT3CARM1PRMT6PRMT1PRMT8
Hydrochloric Acid SCHEMBL8311468 0.80 PRMT3 (0.60) PRMT3CARM1PRMT6PRMT1PRMT8

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
WO-2003054051-A1 METHOD AND COMPOSITION FOR RECOVERING HYDROCARBON FLUIDS FROM A SUBTERRANEAN RESERVOIR ONDEO NALCO ENERGY SERVICES, L.P. (US) 2003-07-03 WO disclosed
US-6569983-B1 Using Jeffamines\"; fracturing subterranean formation ONDEO NALCO ENERGY SERVICES, L.P. 2003-05-27 US disclosed