Sulfuric Acid

Sulfuric Acid

SCHEMBL1629207

CCCCCCCCCc1ccc2ccccc2c1CCCCCCCCC.O=S(=O)(O)O

nearest known ligand 0.48

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
SLC2A1 P11166 3/20 0.48
NCEH1 Q6PIU2 1/20 0.46
TYR P14679 2/20 0.44
KDM4E B2RXH2 2/20 0.43
ALDH1A1 P00352 2/20 0.43
HPGD P15428 2/20 0.43
HSD17B10 Q99714 2/20 0.43
CYP3A4 P08684 2/20 0.43
MAPT P10636 2/20 0.43
USP2 O75604 1/20 0.43
GLA P06280 1/20 0.43
GAA P10253 1/20 0.43
CASP1 P29466 1/20 0.43
CASP7 P55210 1/20 0.43
LIPG Q9Y5X9 1/20 0.43
MEN1 O00255 1/20 0.42
TP53 P04637 1/20 0.42
ALOX5 P09917 1/20 0.42
ALOX15 P16050 1/20 0.42
TSHR P16473 1/20 0.42

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 SCHEMBL11333298 1.00 SLC2A1 (0.48) SLC2A1NCEH1TYRKDM4EALDH1A1
Sulfuric Acid SCHEMBL416631 1.00 SLC2A1 (0.48) SLC2A1NCEH1TYRKDM4EALDH1A1
Sulfuric Acid SCHEMBL10939908 0.99 SLC2A1 (0.47) SLC2A1NCEH1TYRKDM4EALDH1A1
Sulfamate SCHEMBL9632587 0.96 SLC2A1 (0.47) SLC2A1NCEH1TYRKDM4EALDH1A1
Sulfuric Acid SCHEMBL6742835 0.94 NCEH1 (0.51) SLC2A1NCEH1KDM4EALDH1A1HPGD
Sulfuric Acid SCHEMBL6136219 0.93 NCEH1 (0.50) SLC2A1NCEH1KDM4EALDH1A1HPGD
SCHEMBL11381159 0.91 TYR (0.47) NCEH1TYRKDM4EALDH1A1HPGD
SCHEMBL284699 0.91 TYR (0.47) NCEH1TYRKDM4EALDH1A1HPGD
SCHEMBL236078 0.91 TYR (0.47) NCEH1TYRKDM4EALDH1A1HPGD
SCHEMBL284188 0.91 TYR (0.47) NCEH1TYRKDM4EALDH1A1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090289215-A1 ANTIFREEZE COOLANT COMPOSITION HAVING HIGH HEAT-OXIDATION RESISTANCE HYUNDAI MOTOR COMPANY (KR) 2009-11-26 US claimed
CN-1718611-A Preparation method of conductive polyaniline SHANGHAI COLLEGE OF APPLIED TE (CN) 2006-01-11 CN claimed
CN-1583830-A Method for direct preparation of polyaniline solution from aniline monomer XIBEI NUCLEAR TECHNOLOGY INST (CN) 2005-02-23 CN claimed
CN-102977689-B Anti-rust pigment QINGDAO WENCHUANG TECH CO LTD 2014-07-30 CN disclosed
CN-102226045-B Aluminum-tripolyphosphate-doped polyaniline antirust pigment and preparation method thereof GUIYANG FINEW CHEMICAL CO LTD 2014-05-07 CN disclosed
CN-102977689-A Anti-rust pigment QINGDAO ADVANCED MARINE MATERIAL TECHNOLOGY CO LTD 2013-03-20 CN disclosed
CN-102226045-A Aluminum-tripolyphosphate-doped polyaniline antirust pigment and preparation method thereof GUIYANG SHENDI CHEMICAL CO LTD 2011-10-26 CN disclosed
US-7927566-B2 Extraction of radionuclides by crown ether-containing extractants Designing-Contructing and Industrial-Inculcating Enterprise “Daymos Ltd.” (RU) 2011-04-19 US disclosed
CN-101538365-B Method for preparing organic/inorganic acid composite doped conductive polyaniline UNIV KUNMING SCIENCE & TECHNOLOGY 2011-03-30 CN disclosed
US-20090289215-A1 ANTIFREEZE COOLANT COMPOSITION HAVING HIGH HEAT-OXIDATION RESISTANCE HYUNDAI MOTOR COMPANY (KR) 2009-11-26 US disclosed
US-20090289215-A1 ANTIFREEZE COOLANT COMPOSITION HAVING HIGH HEAT-OXIDATION RESISTANCE HYUNDAI MOTOR COMPANY (KR) 2009-11-26 US disclosed
CN-100487023-C Preparation method of composite acids doped with conductive polyaniline UNIV CHONGQING (CN) 2009-05-13 CN disclosed
US-20080014133-A1 Extraction Of Radionuclides By Crown Ether-Containing Extractants DESIGN-CONSTRUCTION AND INDUSTRIAL-INNOVATION ENTERPRISE, LTD. "DAYMOS" (RU) 2008-01-17 US disclosed
CN-1276940-C Method for direct preparation of polyaniline solution from aniline monomer NORTHWEST INST NUCLEAR TECH (CN) 2006-09-27 CN disclosed
CN-1733820-A Preparation method of composite acids doped with conductive polyaniline UNIV CHONGQING (CN) 2006-02-15 CN disclosed
CN-1718611-A Preparation method of conductive polyaniline SHANGHAI COLLEGE OF APPLIED TE (CN) 2006-01-11 CN disclosed
CN-1583830-A Method for direct preparation of polyaniline solution from aniline monomer XIBEI NUCLEAR TECHNOLOGY INST (CN) 2005-02-23 CN disclosed
EP-0914662-A1 METHOD OF INCREASING POLYANILINE CONDUCTIVITY Zipperling Kessler & Co (GmbH & Co) (DE) 1999-05-12 EP disclosed
US-5780572-A POLAR SOLVENT EXTRACTION OF EXCESS NONCONDUCTIVE ACID FROM POLYANILINE-ACID SALT MATERIAL MONSANTO COMPANY (US) 1998-07-14 US disclosed
WO-1998005042-A1 METHOD OF INCREASING POLYANILINE CONDUCTIVITY ZIPPERLING KESSLER & CO. (GMBH & CO.) (DE) 1998-02-05 WO disclosed