Sulfuric Acid

Sulfuric Acid

SCHEMBL1100829

C=CCNC.O=S(=O)(O)O

nearest known ligand 0.35

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 17)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 3/20 0.35
KDM4E B2RXH2 1/20 0.35
CYP2D6 P10635 1/20 0.35
CYP2C19 P33261 1/20 0.35
BLM P54132 1/20 0.35
TSHR P16473 2/20 0.34
SMN1; SMN2 Q16637 2/20 0.34
MAPT P10636 1/20 0.34
ALDH1A1 P00352 2/20 0.33
CA12 O43570 1/20 0.32
CA1 P00915 1/20 0.32
CA2 P00918 1/20 0.32
CA9 Q16790 1/20 0.32
FAAH O00519 1/20 0.32
KMT2A Q03164 1/20 0.32
CA5A P35218 1/20 0.32
CA5B Q9Y2D0 1/20 0.32

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 SCHEMBL1100828 1.00 NPSR1 (0.35) NPSR1KDM4ECYP2D6CYP2C19BLM
SCHEMBL2597 0.83
Bicarbonate SCHEMBL28501524 0.81
Toluene SCHEMBL10456174 0.81 NPSR1 (0.44) NPSR1KDM4ETSHRSMN1; SMN2MAPT
Toluene SCHEMBL10456176 0.81 NPSR1 (0.44) NPSR1KDM4ETSHRSMN1; SMN2MAPT
Bromide SCHEMBL460262 0.80
SCHEMBL31507590 0.80
SCHEMBL29248306 0.80
Water SCHEMBL6400627 0.80
Iodide SCHEMBL28838220 0.80

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 49 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11312795-B2 Transition metal complex for use in or as a catalyst for olefin polymerization SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2022-04-26 US disclosed
CN-110799552-B Transition metal complexes for use in or as catalysts for olefin polymerization SABIC环球技术有限责任公司 2022-02-22 CN disclosed
EP-3630851-B1 PREPARATION OF POLYMER DISPERSIONS SABIC GLOBAL TECHNOLOGIES BV (NL) 2021-07-07 EP disclosed
EP-3681915-A1 AQUEOUS POLYMER DISPERSIONS, A METHOD FOR THEIR PREPARATION AND THE USE THEREOF AS POUR-POINT DEPRESSANTS FOR CRUDE OIL, PETROLEUM, AND PETROLEUM PRODUCTS BASF Corporation (US) 2020-07-22 EP disclosed
CN-111344313-A Aqueous polymer dispersions, method for the production thereof and use thereof as pour point depressants for crude oils, petroleum and petroleum products 巴斯夫公司 2020-06-26 CN disclosed
US-20200087425-A1 TRANSITION METAL COMPLEX FOR USE IN OR AS A CATALYST FOR OLEFIN POLYMERIZATION SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2020-03-19 US disclosed
CN-110799552-A Transition metal complexes for use in or as catalysts for olefin polymerization SABIC环球技术有限责任公司 2020-02-14 CN disclosed
WO-2019048663-A1 AQUEOUS POLYMER DISPERSIONS, A METHOD FOR THEIR PREPARATION AND THE USE THEREOF AS POUR-POINT DEPRESSANTS FOR CRUDE OIL, PETROLEUM, AND PETROLEUM PRODUCTS BASF CORPORATION (US) 2019-03-14 WO disclosed
EP-3426702-A1 AQUEOUS POLYMER DISPERSIONS, A METHOD FOR THEIR PREPARATION AND THE USE THEREOF AS POUR-POINT DEPRESSANTS FOR CRUDE OIL, PETROLEUM, AND PETROLEUM PRODUCTS BASF SE (DE) 2019-01-16 EP disclosed
EP-3409697-A1 PREPARATION OF POLYMER DISPERSIONS SABIC Global Technologies B.V. (NL) 2018-12-05 EP disclosed
US-20080167418-A1 Method for Producing an Aqueous Polyamide Dispersion BASF AKTIENGESELLSCHAFT (DE) 2008-07-10 US disclosed
US-20080132674-A1 Method for the Production of an Aqueous Polymer Dispersion BASF AKTIENGESELLSCHAFT (DE) 2008-06-05 US disclosed
CN-101180322-A Process for producing aqueous polymer dispersions BASF AG (DE) 2008-05-14 CN disclosed
US-20050250920-A1 Preparation of aqueous polymer dispersions BASF AKTIENGESELLSCHAFT (DE) 2005-11-10 US disclosed
US-6800699-B2 REACTING OLEFINICALLY UNSATURATED COMPOUNDS IN AQUEOUS MEDIUM IN THE PRESENCE OF A COMPLEX TRANSITION METAL COMPOUND BASF AKTIENGESELLSCHAFT (DE) 2004-10-05 US disclosed
US-20040167259-A1 Method for producing aqueous copolymer dispersions of copolymers consisting of carbon monoxide and olefinically unsaturated compounds BASF AKTIENGESELLSCHAFT (DE) 2004-08-26 US disclosed
US-20040030040-A1 Method of producing aqueous copolymer dispersions from copolymers that comprise carbon monoxide and at least one olefinically unsaturated compound BASF AKTIENGESELLSCHAFT (DE) 2004-02-12 US disclosed
US-20030114570-A1 Process for the production of aqueous polymer dispersions BASF AKTIENGESELLSCHAFT (DE) 2003-06-19 US disclosed
US-6541564-B2 Copolymerization of carbon monoxide and the olefinically unsaturated carried out in an aqueous medium in the presence of metal complexes, dispersant, organic hydroxy compound, wherein the soluble macromolecular host compound BASF AKTIENGESELLSCHAFT (DE) 2003-04-01 US disclosed
US-20020198359-A1 Priparation of copolymers of carbon monoxide and an olefinically unsaturated compound in an aqueous medium BASF AKIENGESELLSCHAFT (DE) 2002-12-26 US disclosed