Sulfuric Acid

Sulfuric Acid

SCHEMBL5581558

CN=C(N)N.O=S(=O)(O)O

nearest known ligand 0.62

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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
BLM P54132 4/20 0.62
KDM4E B2RXH2 2/20 0.62
CA5A P35218 2/20 0.43
CA5B Q9Y2D0 2/20 0.43
NPSR1 Q6W5P4 2/20 0.43
CYP2D6 P10635 1/20 0.43
CYP2C19 P33261 1/20 0.43
F2 P00734 4/20 0.39
PRSS1 P07477 4/20 0.39
PRSS2 P07478 4/20 0.39
PRSS3 P35030 4/20 0.39
PMP22 Q01453 1/20 0.39
TSHR P16473 2/20 0.38
NOS1 P29475 2/20 0.38
CA1 P00915 1/20 0.38
CA2 P00918 1/20 0.38
NT5E P21589 1/20 0.38
CA4 P22748 1/20 0.38
CA6 P23280 1/20 0.38
CA7 P43166 1/20 0.38

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
SCHEMBL307359 0.80
Sulfuric Acid SCHEMBL18584 0.80 BLM (0.47) BLMKDM4ECA5ACA5BNPSR1
Sulfuric Acid SCHEMBL1940141 0.80 BLM (0.47) BLMKDM4ECA5ACA5BNPSR1
Sulfuric Acid SCHEMBL3892286 0.80 BLM (0.47) BLMKDM4ECA5ACA5BNPSR1
Pimagedine SCHEMBL439904 0.77 BLM (1.00) BLMKDM4ECA5ACA5BNPSR1
Pimagedine SCHEMBL5968075 0.77 BLM (1.00) BLMKDM4ECA5ACA5BNPSR1
Bromide SCHEMBL11505136 0.76
Water SCHEMBL1971739 0.76
Hydrochloric Acid SCHEMBL526048 0.76
Hydroxyguanidine SCHEMBL961747 0.74 BLM (0.67) BLMKDM4ECA5ACA5BNPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4247632-A QUANTITATIVE ANALYSIS OF METHYLAMINE AND UREA PRODUCTS; CULTURES USING ALCALIGENES KIKKOMAN SHOYU CO., LTD. (JP) 1981-01-27 US claimed
US-20240218344-A1 LIQUID THROMBIN REAGENT INSTRUMENTATION LABORATORY COMPANY 2024-07-04 US disclosed
EP-4389140-A1 LIQUID THROMBIN REAGENT CONTAINING GUANIDINE DERIVATIVES Instrumentation Laboratory Company (US) 2024-06-26 EP disclosed
CN-114072378-A Process for preparing metastable crystal modifications of N- (aminoiminomethyl) -2-aminoacetic acid (III) 澳泽化学特罗斯特贝格有限公司 2022-02-18 CN disclosed
CN-101190897-B Method for synthesizing 4-(4-fluorophenyl)-6-isopropyl-2-methylaminopyrimidine-5-formic acid ester TIANJIN TASLY GROUP CO LTD 2011-05-11 CN disclosed
CN-101190897-A Method for synthesizing 4-(4-fluorophenyl)-6-isopropyl-2-methylaminopyrimidine-5-formic acid ester TIANJIN TASLY GROUP CO LTD (CN) 2008-06-04 CN disclosed
US-20070225308-A1 2-Amino Quinazoline Derivative KYOWA HAKKO KOGYO CO.,LTD. (JP) 2007-09-27 US disclosed
EP-1726584-A1 2-AMINOQUINAZOLINE DERIVATIVE KYOWA HAKKO KOGYO CO., LTD. (JP) 2006-11-29 EP disclosed
EP-0217787-A4 AMIDINOUREA PROCESS AND PHARMACEUTICAL COMPOSITION. RORER INTERNAT OVERSEAS INC (US) 1988-07-21 EP disclosed
EP-0217787-A1 AMIDINOUREA PROCESS AND PHARMACEUTICAL COMPOSITION RORER INTERNATIONAL (OVERSEAS) INC. (a Delaware corporation) (US) 1987-04-15 EP disclosed
US-4503147-A CULTURE PRODUCT OF BACILLUS KIKKOMAN CORPORATION (JP) 1985-03-05 US disclosed
EP-0116639-A1 ACYL GUANIDINES RORER INTERNATIONAL (OVERSEAS) INC. (US) 1984-08-29 EP disclosed
WO-1984000875-A1 ACYL GUANIDINES RORER INT OVERSEAS (US) 1984-03-15 WO disclosed
US-4418209-A ANTIULCER, ANTIARRYTHMIC, ANTIDIARRHEAL, ANTISPASMODIC, ANTIPARASITIC, AND ANTISECRETORY AGENTS WILLIAM H. RORER, INC. (US) 1983-11-29 US disclosed
EP-0079377-A1 HETEROCYCLIC ALKYLENE AMIDINOUREAS RORER INTERNATIONAL (OVERSEAS) INC. (US) 1983-05-25 EP disclosed
WO-1982004048-A1 HETEROCYCLIC ALKYLENE AMIDINOUREAS RORER INT OVERSEAS (US) 1982-11-25 WO disclosed
US-4247632-A QUANTITATIVE ANALYSIS OF METHYLAMINE AND UREA PRODUCTS; CULTURES USING ALCALIGENES KIKKOMAN SHOYU CO., LTD. (JP) 1981-01-27 US disclosed
US-4178387-A ADMINISTERING AMIDINOUREAS WILLIAM H. RORER, INC. (US) 1979-12-11 US disclosed
US-4147804-A ANTIARRHYTHMIA AGENTS WILLIAM H. RORER, INC. (US) 1979-04-03 US disclosed
US-4085211-A DIURETICS, NATRIURETICS MERCK & CO., INC. (US) 1978-04-18 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 (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-20070225308-A1 2-Amino Quinazoline Derivative AGTR2, ABL1, AGTR1 BLM 2208/4885KDM4E 1708/4885CA5A 2353/4885
US-20240218344-A1 LIQUID THROMBIN REAGENT TFPI, F2, PLG BLM 1567/4885KDM4E 600/4885CA5A 3900/4885

“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.