Sulfuric Acid

Sulfuric Acid

SCHEMBL6511524

CCC(C)(C)c1ccc2cccccc1-2.O=S(=O)(O)O.[NaH]

nearest known ligand 0.41

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
PTGS2 P35354 5/20 0.41
SMN1; SMN2 Q16637 2/20 0.40
NPC1 O15118 1/20 0.40
LMNA P02545 1/20 0.40
MAPK1 P28482 1/20 0.40
CASP3 P42574 1/20 0.40
RAB9A P51151 1/20 0.40
ATM Q13315 1/20 0.40
SENP8 Q96LD8 1/20 0.40
SENP7 Q9BQF6 1/20 0.40
SENP6 Q9GZR1 1/20 0.40
PPARG P37231 1/20 0.36
PPARA Q07869 1/20 0.36
HSP90AA1 P07900 2/20 0.35
HSP90AB1 P08238 2/20 0.35
MAPT P10636 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
DRD1 P21728 1/20 0.34
PDCD1 Q15116 1/20 0.33
CD274 Q9NZQ7 1/20 0.33

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
SCHEMBL677798 0.88 MAPK1 (0.40) PTGS2SMN1; SMN2NPC1LMNAMAPK1
SCHEMBL127574 0.83 MAPK1 (0.41) PTGS2SMN1; SMN2NPC1LMNAMAPK1
SCHEMBL27797465 0.77 ABL1 (0.44) SMN1; SMN2NPC1LMNAMAPK1CASP3
SCHEMBL31510648 0.72 HNF4A (0.43) SMN1; SMN2NPC1LMNAMAPK1CASP3
SCHEMBL26632610 0.72 HNF4A (0.43) SMN1; SMN2NPC1LMNAMAPK1CASP3
SCHEMBL6342144 0.71 PPARG (0.35) PTGS2SMN1; SMN2NPC1LMNAMAPK1
SCHEMBL6342141 0.71 SMN1; SMN2 (0.41) SMN1; SMN2NPC1LMNAMAPK1CASP3
SCHEMBL10524404 0.71 PTGS2 (0.37) PTGS2SMN1; SMN2MAPK1PDCD1CD274
SCHEMBL9695975 0.70 PDCD1 (0.37) SMN1; SMN2NPC1LMNAMAPK1CASP3
SCHEMBL22432024 0.70 NOTUM (0.39) SMN1; SMN2NPC1LMNAMAPK1CASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2005112883-A1 PRESERVED PHARMACEUTICAL COMPOSITIONS COMPRISING CYCLODEXTRINS ALLERGAN, INC. (US) 2005-12-01 WO disclosed
US-6969706-B1 Preserved pharmaceutical compositions comprising cyclodextrins ALLERGAN, INC. (US) 2005-11-29 US disclosed
US-20050256083-A1 Ophthalmic liquid containing a cyclodextrin, a guanidine-based cationic compound, and sorbic acid ALLERGAN, INC. (US) 2005-11-17 US disclosed
US-20040214797-A1 Preserved pharmaceutical compositions comprising cyclodextrins ALLERGAN, INC. 2004-10-28 US disclosed
EP-0877600-B1 PRESERVATIVE SYSTEMS FOR PHARMACEUTICAL COMPOSITIONS CONTAINING CYCLODEXTRINS ALCON MFG LTD (US) 2003-10-22 EP disclosed
US-5985310-A CHELATING AGENT AND AN ANTIMICROBIAL PRESERVATIVE WHICH IS BORIC ACID AND A COMPOUND SELECTED FROM BENZALKONIUM HALIDE COMPOUNDS, POLYMERIC QUATERNARY AMMONIUM COMPOUNDS, AND QUATEMARY AMMONIUM ALKYLENE GLYCOL PHOSPHOLIPID DERIVATIVES ALCON LABORATORIES, INC. (US) 1999-11-16 US disclosed
EP-0877600-A1 PRESERVATIVE SYSTEMS FOR PHARMACEUTICAL COMPOSITIONS CONTAINING CYCLODEXTRINS ALCON LABORATORIES, INC. (US) 1998-11-18 EP disclosed
WO-1998006381-A1 PRESERVATIVE SYSTEMS FOR PHARMACEUTICAL COMPOSITIONS CONTAINING CYCLODEXTRINS ALCON LABORATORIES, INC. (US) 1998-02-19 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 (2 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-20040214797-A1 Preserved pharmaceutical compositions comprising cyclodextrins DDOST, RPN1, GANC PTGS2 975/4885SMN1; SMN2 3173/4885NPC1 726/4885
US-20050256083-A1 Ophthalmic liquid containing a cyclodextrin, a guanidine-based cationic compound, and sorbic acid SORBS1, GANC, UACA PTGS2 2711/4885SMN1; SMN2 1857/4885NPC1 505/4885

“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.