Sulfuric Acid

Sulfuric Acid

SCHEMBL711964

CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.O=S(=O)(O)O

nearest known ligand 0.71

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 8)

geneUniProtsupporting neighboursconfidence
HTT P42858 2/20 0.71
DNM1 Q05193 12/20 0.68
KMT2A Q03164 1/20 0.58
HSP90AA1 P07900 2/20 0.56
RAD52 P43351 2/20 0.56
PLA2G1B P04054 1/20 0.52
ATG4B Q9Y4P1 1/20 0.52
LMNA P02545 1/20 0.48

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 SCHEMBL27686667 1.00 HTT (0.71) HTTDNM1KMT2AHSP90AA1RAD52
Didecyldimethylammonium SCHEMBL7774195 1.00 HTT (0.71) HTTDNM1KMT2AHSP90AA1RAD52
Sulfuric Acid SCHEMBL28640579 1.00 HTT (0.71) HTTDNM1KMT2AHSP90AA1RAD52
Didecyldimethylammonium SCHEMBL28027086 1.00 HTT (0.71) HTTDNM1KMT2AHSP90AA1RAD52
Sulfuric Acid SCHEMBL23248612 1.00 HTT (0.71) HTTDNM1KMT2AHSP90AA1RAD52
Sulfuric Acid SCHEMBL25278416 1.00 HTT (0.71) HTTDNM1KMT2AHSP90AA1RAD52
Didecyldimethylammonium SCHEMBL28145567 0.98 HTT (0.68) HTTDNM1KMT2AHSP90AA1RAD52
Sulfuric Acid SCHEMBL2378915 0.98 HTT (0.68) HTTDNM1KMT2AHSP90AA1RAD52
Sulfuric Acid SCHEMBL4471496 0.96 DNM1 (0.74) HTTDNM1KMT2AHSP90AA1RAD52
Sulfuric Acid SCHEMBL1427099 0.96 DNM1 (0.74) HTTDNM1KMT2AHSP90AA1RAD52

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2167124-B1 THE USE OF MONOMYCOLYL GLYCEROL (MMG) AS AN ADJUVANT STATENS SERUMINSTITUT (DK) 2012-08-01 EP claimed
JP-6208253-A None JP disclosed
CN-115581638-A Cleaning agent 株式会社资生堂 2023-01-10 CN disclosed
CN-107532129-B Efficient small volume nucleic acid synthesis 生命技术公司 2022-09-13 CN disclosed
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
US-11261392-B2 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) 2022-03-01 US disclosed
EP-3681915-B1 AQUEOUS POLYMER DISPERSIONS, A METHOD FOR THEIR PREPARATION AND THE USE THEREOF AS POUR-POINT DEPRESSANTS FOR CRUDE OIL, PETROLEUM, AND PETROLEUM PRODUCTS BASF CORP (US) 2021-11-24 EP disclosed
EP-3630851-B1 PREPARATION OF POLYMER DISPERSIONS SABIC GLOBAL TECHNOLOGIES BV (NL) 2021-07-07 EP disclosed
CN-112638355-A Cosmetic and cleaning product 株式会社资生堂 2021-04-09 CN disclosed
US-10851323-B2 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 2020-12-01 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
US-5695904-A CREATING LATENT IMAGE, DEVELOPING WITH SEMI-DRY DEVELOPER PREPARED BY REMOVING LIQUID FROM LIQUID DEVELOPER XEROX CORPORATION (US) 1997-12-09 US disclosed
US-5336579-A Color developer compositions containing bare carrier cores and coated carrier cores XEROX CORPORATION (US) 1994-08-09 US disclosed
JP-H06208253-A TONER COMPOSITION XEROX CORP 1994-07-26 JP disclosed
US-5324614-A Erase setting for copiers and printers XEROX CORPORATION (US) 1994-06-28 US disclosed
EP-0586955-A2 Color developer compositions containing bare carrier cores XEROX CORPORATION (US) 1994-03-16 EP disclosed
EP-0586177-A2 Copying or printing process and apparatus XEROX CORPORATION (US) 1994-03-09 EP disclosed