Sulfuric Acid

Sulfuric Acid

SCHEMBL2638826

CCCC[n+]1ccccc1.O=S(=O)([O-])O

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

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 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 4/20 0.59
CHRM2 P08172 2/20 0.59
ADRA2A P08913 2/20 0.59
ADORA3 P0DMS8 2/20 0.59
CHRM1 P11229 2/20 0.59
SLC6A2 P23975 2/20 0.59
SLC6A4 P31645 2/20 0.59
SLC6A3 Q01959 2/20 0.59
ABCB11 O95342 1/20 0.59
ESR1 P03372 1/20 0.59
PGR P06401 1/20 0.59
HTR1A P08908 1/20 0.59
DRD1 P21728 1/20 0.59
TBXA2R P21731 1/20 0.59
PTGS1 P23219 1/20 0.59
PDE4A P27815 1/20 0.59
ADRA1A P35348 1/20 0.59
OPRM1 P35372 1/20 0.59
DRD3 P35462 1/20 0.59
KCNH2 Q12809 1/20 0.59

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 SCHEMBL28083761 0.93 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL9784505 0.93 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
Cetylpyridinium SCHEMBL714215 0.93 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL366910 0.93 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL9784621 0.93 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL11121741 0.93 ACHE (0.71) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL3005563 0.92 ACHE (0.63) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL4247890 0.92 ACHE (0.63) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL27681675 0.92 ACHE (0.63) ACHECHRM2ADRA2AADORA3CHRM1
Sulfuric Acid SCHEMBL27700907 0.92 ACHE (0.63) ACHECHRM2ADRA2AADORA3CHRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119175052-A Industrial preparation method of acrolein 中国石油化工股份有限公司 2024-12-24 CN claimed
CN-117736092-A Synthesis of polyglycol fatty acid ester and application of polyglycol fatty acid ester in chemical fiber spinning 广东省造纸研究所有限公司 2024-03-22 CN claimed
WO-2023070961-A1 ACID/PHOTOCATALYTIC OXIDATION REACTION OF BENZYLIC CARBON-HYDROGEN BOND IN AROMATIC COMPOUND 南京工业大学 2023-05-04 WO claimed
CN-113480582-A Green and cyclic comprehensive utilization method for agricultural and forestry solid wastes 广东工业大学 2021-10-08 CN claimed
CN-104945254-B A kind of synthetic method of medicine intermediate condensed ring ester type compound 中山福运生物科技有限公司 2016-10-19 CN claimed
CN-105038997-A Method for synchronously preparing biodiesel and glycerol carbonate through ionic liquid and catalytic grease GUANGZHOU INST ENERGY CONV CAS 2015-11-11 CN claimed
EP-1812382-B1 METHOD FOR PRODUCING POLYISOCYANATES BASF SE (DE) 2013-01-23 EP claimed
JP-4794561-B2 2011-10-19 JP claimed
EP-1789160-B1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF SE (DE) 2009-11-18 EP claimed
US-20090112017-A1 METHOD FOR PRODUCING POLYISOCYANATES BASF AKTIENGESSELLSCHAFT (DE) 2009-04-30 US claimed
EP-1789160-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2007-05-30 EP claimed
WO-2006029788-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2006-03-23 WO claimed
CN-119175052-A Industrial preparation method of acrolein 中国石油化工股份有限公司 2024-12-24 CN disclosed
CN-117736092-A Synthesis of polyglycol fatty acid ester and application of polyglycol fatty acid ester in chemical fiber spinning 广东省造纸研究所有限公司 2024-03-22 CN disclosed
WO-2023070961-A1 ACID/PHOTOCATALYTIC OXIDATION REACTION OF BENZYLIC CARBON-HYDROGEN BOND IN AROMATIC COMPOUND 南京工业大学 2023-05-04 WO disclosed
CN-111435705-B Repairing agent and repairing method thereof and method for preparing photoelectric film 杭州纤纳光电科技有限公司 2023-04-07 CN disclosed
EP-1789160-B1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF SE (DE) 2009-11-18 EP disclosed
US-20090112017-A1 METHOD FOR PRODUCING POLYISOCYANATES BASF AKTIENGESSELLSCHAFT (DE) 2009-04-30 US disclosed
EP-1789160-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2007-05-30 EP disclosed
WO-2006029788-A1 METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE BASF AKTIENGESELLSCHAFT (DE) 2006-03-23 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090112017-A1 METHOD FOR PRODUCING POLYISOCYANATES PGLS, INMT, PNMT ACHE 796/4885CHRM2 2669/4885ADRA2A 3286/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.