Sulfuric Acid

Sulfuric Acid

SCHEMBL7741636

C1CNC1.C1CNC1.O=S(=O)(O)O

nearest known ligand 0.50

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
CA5A P35218 2/20 0.50
CA5B Q9Y2D0 2/20 0.50
TSHR P16473 5/20 0.43
LMNA P02545 2/20 0.43
CYP3A4 P08684 1/20 0.43
GABRA1 P14867 1/20 0.43
GABRG2 P18507 1/20 0.43
NFKB1 P19838 1/20 0.43
GABRB3 P28472 1/20 0.43
GABRA5 P31644 1/20 0.43
GABRA3 P34903 1/20 0.43
GABRA2 P47869 1/20 0.43
GABRA6 Q16445 1/20 0.43
SMN1; SMN2 Q16637 2/20 0.40
ALDH1A1 P00352 2/20 0.40
CXCR4 P61073 1/20 0.40
APLNR P35414 2/20 0.36
KDM4E B2RXH2 3/20 0.33
CA1 P00915 1/20 0.33
CA2 P00918 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
Sulfuric Acid SCHEMBL7741639 1.00
Pyrrolidine SCHEMBL3835047 0.93 ALDH1A1 (0.53) CA5ACA5BTSHRLMNACYP3A4
Pyrrolidine SCHEMBL28642083 0.93 ALDH1A1 (0.53) CA5ACA5BTSHRLMNACYP3A4
Pyrrolidine SCHEMBL27815363 0.89 ALDH1A1 (0.50) CA5ACA5BTSHRLMNACYP3A4
Piperidine SCHEMBL4439035 0.89 ALDH1A1 (0.60) CA5ACA5BTSHRLMNACYP3A4
Sulfuric Acid SCHEMBL28813640 0.89 ALDH1A1 (0.60) CA5ACA5BTSHRLMNACYP3A4
Azepane SCHEMBL29144238 0.89 ALDH1A1 (0.60) CA5ACA5BTSHRLMNACYP3A4
Piperidine SCHEMBL5874676 0.89 ALDH1A1 (0.60) CA5ACA5BTSHRLMNACYP3A4
Sulfuric Acid SCHEMBL4097784 0.87
Sulfuric Acid SCHEMBL11184576 0.87 CA5A (0.55) CA5ACA5BTSHRLMNACYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260007745-A1 ALDH Inhibitors to Promote Immune Cell Expansion UNIV PITTSBURGH COMMONWEALTH SYS HIGHER EDUCATION (US) 2026-01-08 US disclosed
US-6417373-B1 AZA AZETIDINIUM SULFATE COMPOUNDS CHEMICAL INTERMEDIATES FOR PROPELLANTS AND EXPLOSIVES THE UNITED STATES OF AMERICA AS REPRESENTED BY SECRETARY OF ARMY 2002-07-09 US 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-20260007745-A1 ALDH Inhibitors to Promote Immune Cell Expansion ALDH1A1, ALDH3A1, ALDH2 CA5A 896/4885CA5B 1000/4885TSHR 4002/4885

“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.