Sulfuric Acid

Sulfuric Acid

SCHEMBL1508282

CC[N+](CC)(CC)c1ccccc1.O=S(=O)([O-])O

nearest known ligand 0.39

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Known targets — ChEMBL curated mechanism

CYP51cyp51Acyp51c

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 18)

geneUniProtsupporting neighboursconfidence
PSIP1 O75475 1/20 0.39
TSHR P16473 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
CHRM4 P08173 1/20 0.36
CHRM1 P11229 1/20 0.36
CHRM3 P20309 1/20 0.36
CES2 O00748 2/20 0.35
CES1 P23141 2/20 0.35
CA12 O43570 1/20 0.35
CA2 P00918 1/20 0.35
CA9 Q16790 1/20 0.35
HSD11B1 P28845 1/20 0.35
NPSR1 Q6W5P4 1/20 0.34
PTGS2 P35354 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
ESR1 P03372 1/20 0.34
HSP90AA1 P07900 1/20 0.34
TLR9 Q9NR96 1/20 0.34

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 SCHEMBL31286303 0.92 PSIP1 (0.41) PSIP1CHRM4CHRM1CHRM3CES2
SCHEMBL29049262 0.90 PSIP1 (0.40) PSIP1TSHRSMN1; SMN2CHRM4CHRM1
SCHEMBL21957777 0.90 PSIP1 (0.40) PSIP1CA12CA2CA9PTGS2
Sulfuric Acid SCHEMBL1534138 0.85 DNM1 (0.41) SMN1; SMN2CHRM1CHRM3CES2CES1
SCHEMBL21957767 0.85 BCHE (0.41) PSIP1CHRM4CHRM1CHRM3CA12
Sulfuric Acid SCHEMBL10802033 0.84 PSIP1 (0.39) PSIP1TSHRSMN1; SMN2CES2CES1
Bicarbonate SCHEMBL21957729 0.83 CES2 (0.43) TSHRCHRM4CHRM1CHRM3CES2
Trifluoromethanesulfonic Acid SCHEMBL21957811 0.83 KCNH2 (0.44) PSIP1
Bicarbonate SCHEMBL21957730 0.83 CHRM1 (0.43) TSHRSMN1; SMN2CHRM4CHRM1CHRM3
SCHEMBL11417691 0.83 APOBEC3A (0.42) TSHRSMN1; SMN2CHRM4CHRM1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8206673-B2 Method of preparing boron-nitrogen compounds WILDCAT DISCOVERY TECHNOLOGIES (US) 2012-06-26 US disclosed
US-20110064640-A1 METHOD OF PREPARING BORON-NITROGEN COMPOUNDS WILDCAT DISCOVERY TECHNOLOGIES (US) 2011-03-17 US disclosed
US-4144265-A CHLOROMETHYLATION, CYANATION OF TRIFLUOROMETHYL BENZENE THE DOW CHEMICAL COMPANY (US) 1979-03-13 US disclosed
US-4141916-A 3,4,5-Trichloro-N,N-Di(loweralkyl)-2-((chloromethyl)thio)benzenesulfonamides THE DOW CHEMICAL COMPANY (US) 1979-02-27 US disclosed
US-4094873-A Process for preparing phosphorothioates and phenylphosphonothioates THE DOW CHEMICAL COMPANY (US) 1978-06-13 US disclosed
US-4092312-A CATALYST SYSTEM OF A QUATERNARY AMMONIUM SALT AND 1,4-DIAZABICYCLO(2.2.2)OCTANE THE DOW CHEMICAL COMPANY (US) 1978-05-30 US disclosed
US-4061682-A QUATERNARY AMMONIUM OR PHOSPHONIUM SALT THE DOW CHEMICAL COMPANY (US) 1977-12-06 US disclosed
US-4028439-A QUATERNARY AMMONIUM SALT AND IMIDAZOLE CATALYSTS THE DOW CHEMICAL COMPANY (US) 1977-06-07 US disclosed
US-4016225-A WITH QUATERNARY AMMONIUM SALT AND 1,4-DIAZABICYCLO(2.2.2)OCTANE CATALYST THE DOW CHEMICAL COMPANY (US) 1977-04-05 US disclosed
US-4014891-A FROM AN ALKALI METAL ARYL MERCAPTIDE AND BROMOCHLOROMETHANE IN A QUATERNARY AMMONIUM SALT THE DOW CHEMICAL COMPANY (US) 1977-03-29 US disclosed
US-4001293-A Process for production of γ-halonitriles THE DOW CHEMICAL COMPANY (US) 1977-01-04 US disclosed
US-3974199-A Process for production of cyclopropylcyanide THE DOW CHEMICAL COMPANY (US) 1976-08-10 US disclosed
US-3972887-A QUATERNARY AMMONIUM SALT CATALYST THE DOW CHEMICAL COMPANY (US) 1976-08-03 US disclosed
US-3969360-A Catalyzed alkylation of halopyridinates THE DOW CHEMICAL COMPANY (US) 1976-07-13 US disclosed