Sulfuric Acid

Sulfuric Acid

SCHEMBL5587293

CCC[N+](C)(C)CCCNC(=O)CC[C@@H](C)[C@H]1CCC2C3CCC4CCCC[C@]4(C)C3CC[C@@]21C.O=S(=O)(O)O

nearest known ligand 0.68

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
EPHA2 P29317 3/20 0.68
GPBAR1 Q8TDU6 10/20 0.59
AKR1B10 O60218 1/20 0.59
AKR1B1 P15121 1/20 0.59
EFNA1 P20827 1/20 0.59
PSEN1 P49768 1/20 0.59
PSEN2 P49810 1/20 0.59
APH1B Q8WW43 1/20 0.59
NCSTN Q92542 1/20 0.59
APH1A Q96BI3 1/20 0.59
PSENEN Q9NZ42 1/20 0.59
MEN1 O00255 1/20 0.59
LMNA P02545 1/20 0.59
KMT2A Q03164 1/20 0.59
HSD17B10 Q99714 1/20 0.59
TDP1 Q9NUW8 1/20 0.59
ABCC4 O15439 3/20 0.58
VDR P11473 2/20 0.58
NR1H4 Q96RI1 1/20 0.56
ABCC1 P33527 1/20 0.56

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
SCHEMBL1615267 0.97 EPHA2 (0.72) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Sulfuric Acid SCHEMBL2285700 0.96 EPHA2 (0.67) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786177 0.96 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786176 0.96 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786159 0.93 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786157 0.93 EPHA2 (0.71) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
SCHEMBL55596 0.92 EPHA2 (0.68) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Sulfuric Acid SCHEMBL10535471 0.92 EPHA2 (0.68) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786149 0.92 EPHA2 (0.70) EPHA2GPBAR1AKR1B10AKR1B1EFNA1
Iodide SCHEMBL17786150 0.92 EPHA2 (0.70) EPHA2GPBAR1AKR1B10AKR1B1EFNA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2610315-B1 Methine-substituted cyanine dye compounds LIFE TECHNOLOGIES CORP (US) 2016-08-31 EP disclosed
WO-2015058025-A1 VAULTS ENGINEERED FOR HYDROPHOBIC DRUG DELIVERY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2015-04-23 WO disclosed
EP-2037904-B1 BASIC ACETOPHENONES AS INHIBITORS OF NO-SYNTHASES UNIV KIEL CHRISTIAN ALBRECHTS (DE) 2012-09-19 EP disclosed
EP-1262490-B1 GPib-LIPID BOND CONSTRUCT AND USE THEREOF MITSUBISHI PHARMA CORP (JP) 2007-10-03 EP disclosed
US-6926884-B2 GPIb-lipid bond construct and use thereof MITSUBISHI PHARMA CORPORATION (JP) 2005-08-09 US disclosed
EP-1257560-A4 BCL-2-LIKE POLYNUCLEOTIDES, POLYPEPTIDES, AND ANTIBODIES HUMAN GENOME SCIENCES INC (US) 2003-10-01 EP disclosed
US-20030113262-A1 Gpib-lipid bond construct and use thereof IKEDA, YASUO (JP) 2003-06-19 US disclosed
US-20020183369-A1 Bicyclic pyrrolyl amides as glycogen phosphorylase inhibitors DU BOIS DAISY JOE (US) 2002-12-05 US disclosed
EP-1262490-A1 GPib-LIPID BOND CONSTRUCT AND USE THEREOF Mitsubishi Pharma Corporation (JP) 2002-12-04 EP disclosed
EP-1257560-A1 BCL-2-LIKE POLYNUCLEOTIDES, POLYPEPTIDES, AND ANTIBODIES HUMAN GENOME SCIENCES, INC. (US) 2002-11-20 EP disclosed
WO-2000020449-A9 MODIFIED TGF-β SUPERFAMILY PROTEINS STRYKER CORP (US) 2002-08-22 WO disclosed
WO-2001057060-A1 BCL-2-LIKE POLYNUCLEOTIDES, POLYPEPTIDES, AND ANTIBODIES HUMAN GENOME SCIENCES, INC. (US) 2001-08-09 WO disclosed
EP-1117804-A2 CHIMAERIC PROTEINS BETWEEN MEMBERS OF TGF-BETA SUPERFAMILY STRYKER CORPORATION (US) 2001-07-25 EP disclosed
EP-1117805-A2 MODIFIED TGF-BETA SUPERFAMILY PROTEINS STRYKER CORPORATION (a Michigan corporation) (US) 2001-07-25 EP disclosed
WO-2000020607-A9 CHIMAERIC PROTEINS BETWEEN MEMBERS OF TGF-BETA SUPERFAMILY STRYKER CORP (US) 2001-03-29 WO disclosed
WO-2000033075-A1 METHOD AND APPARATUS FOR THE SEPARATION OF COMPONENTS FROM A BIOLOGICAL MATERIAL PROTEOSYS AG (DE) 2000-06-08 WO disclosed
WO-2000020449-A2 MODIFIED TGF-β SUPERFAMILY PROTEINS STRYKER CORPORATION (US) 2000-04-13 WO disclosed
WO-2000020607-A2 CHIMAERIC PROTEINS BETWEEN MEMBERS OF TGF-BETA SUPERFAMILY STRYKER CORPORATION (US) 2000-04-13 WO disclosed
WO-1989003885-A1 METHOD OF REMOVING ENDOTOXIN CONTAMINANTS CENTOCOR, INC. (US) 1989-05-05 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-20020183369-A1 Bicyclic pyrrolyl amides as glycogen phosphorylase inhibitors PYGL, PYGM, PYGB EPHA2 3829/4885GPBAR1 839/4885AKR1B10 500/4885

“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.