Sulfuric Acid

Sulfuric Acid

SCHEMBL2891

CNC(N)=O.O=S(=O)(O)O

nearest known ligand 0.42

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
MAOA known ✓ P21397 1/20 0.39
MAOB known ✓ P27338 1/20 0.39
BLM P54132 4/20 0.42
KDM4E B2RXH2 3/20 0.42
CYP2D6 P10635 1/20 0.41
CYP2C19 P33261 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
CA5A P35218 3/20 0.40
CA5B Q9Y2D0 2/20 0.40
CA2 P00918 5/20 0.39
LMNA P02545 4/20 0.39
TSHR P16473 3/20 0.39
CA9 Q16790 3/20 0.39
NFKB1 P19838 2/20 0.39
PMP22 Q01453 2/20 0.39
CYP3A4 P08684 2/20 0.39
CYP1A2 P05177 1/20 0.39
THPO P40225 1/20 0.39
CRBN Q96SW2 1/20 0.38
ALOX15 P16050 2/20 0.35

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 SCHEMBL27702892 1.00 BLM (0.42) BLMKDM4ECYP2D6CYP2C19NPSR1
Sulfuric Acid SCHEMBL31648906 1.00 BLM (0.42) BLMKDM4ECYP2D6CYP2C19NPSR1
SCHEMBL27723465 0.93 CA2 (0.39) BLMKDM4ECYP2D6CYP2C19NPSR1
SCHEMBL9157890 0.86 LMNA (0.50) BLMKDM4ECA5ACA2LMNA
SCHEMBL10181 0.86
SCHEMBL28150226 0.83 CRBN (0.32) BLMCA5ACA2LMNATSHR
SCHEMBL27486772 0.83 CA2 (0.36) BLMCA5ACA2LMNATSHR
Hydrochloric Acid SCHEMBL180387 0.82
SCHEMBL11876964 0.82
Hydrochloric Acid SCHEMBL6900073 0.82

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117756773-A Preparation process of heliotropin 宿迁市万和泰化工有限公司 2024-03-26 CN claimed
CN-117005110-A Long-acting electret melt-blown cloth and preparation method thereof 孚韦(内蒙古)安全装备有限公司 2023-11-07 CN claimed
CN-115925639-A Antineoplastic fluorouracil and preparation process thereof 上海旭东海普南通药业有限公司 2023-04-07 CN claimed
CN-114210238-A Fluorouracil refining method and device 上海旭东海普南通药业有限公司 2022-03-22 CN claimed
CN-113563233-A Anti-carbonization concrete reinforcing agent and preparation method thereof 石家庄市长安育才建材有限公司 2021-10-29 CN claimed
CN-110396116-B [ N, O ] bidentate nickel and palladium complex of ketone-imidazoline-2-imine ligand, and preparation method and application thereof 东华大学 2020-07-28 CN claimed
CN-106117242-B Tetrahydric thiapyran miazines derivative and the preparation method and application thereof 山东大学 2018-08-03 CN claimed
CN-106117242-A Tetrahydric thiapyran miazines derivative and preparation method and application 山东大学 2016-11-16 CN claimed
EP-1042292-A1 METHOD FOR PRODUCING ISOUREAS Takeda Chemical Industries, Ltd. (JP) 2000-10-11 EP claimed
WO-1999033809-A1 METHOD FOR PRODUCING ISOUREAS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1999-07-08 WO claimed
JP-4089466-A None JP disclosed
JP-61180760-A None JP disclosed
CN-119569613-A Method for preparing O-methyl-N-nitroisourea 武汉青江化工黄冈有限公司 2025-03-07 CN disclosed
US-20250011333-A1 PYRAZOLO-QUINAZOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS NERVIANO MEDICAL SCIENCES SRL (IT) 2025-01-09 US disclosed
EP-4380494-A1 COMPOSITION FOR ISOLATING TISSUE Solventum Intellectual Properties Company (US) 2024-06-12 EP disclosed
US-4617401-A ANTISPASMODIC AGENTS, VASODILATORS SUNTORY LTD. (JP) 1986-10-14 US disclosed
JP-S61180760-A PRODUCTION OF O-METHYLISOUREA ACETIC ACID SALT DAINIPPON INK & CHEM INC 1986-08-13 JP disclosed
EP-0039903-B1 8-SUBSTITUTED PYRROLIZIDINES AND QUATERNARY AMMONIUM SALTS THEREOF SUNTORY KABUSHIKI KAISHA (JP) 1986-04-09 EP disclosed
US-4564382-A HERBICIDES HOECHST AKTIENGESELLSCHAFT (DE) 1986-01-14 US disclosed
EP-0039903-A2 8-Substituted pyrrolizidines and quaternary ammonium salts thereof SUNTORY KABUSHIKI KAISHA (JP) 1981-11-18 EP 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-20250011333-A1 PYRAZOLO-QUINAZOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS MAP3K5, MAP3K9, MAP4K2 MAOA 2206/4885MAOB 1561/4885BLM 2225/4885

“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.