Sulfuric Acid

Sulfuric Acid

SCHEMBL4106019

CSC(=N)N.O=S(=O)([O-])O.[H+]

nearest known ligand 0.75

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CYP51cyp51Acyp51c

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 16)

geneUniProtsupporting neighboursconfidence
CYP2D6 P10635 3/20 0.75
CYP2C19 P33261 2/20 0.75
KDM4E B2RXH2 1/20 0.75
BLM P54132 1/20 0.75
NPSR1 Q6W5P4 1/20 0.75
NOS1 P29475 4/20 0.58
NOS3 P29474 3/20 0.58
NOS2 P35228 3/20 0.58
MAPK1 P28482 2/20 0.58
ALDH1A1 P00352 3/20 0.40
TSHR P16473 2/20 0.40
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
LMNA P02545 2/20 0.34
MAPT P10636 1/20 0.31
CYP1A2 P05177 1/20 0.31

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 SCHEMBL22347074 0.86 BLM (1.00) CYP2D6CYP2C19KDM4EBLMNPSR1
Sulfuric Acid SCHEMBL317855 0.86 BLM (1.00) CYP2D6CYP2C19KDM4EBLMNPSR1
Sulfuric Acid SCHEMBL18206 0.86 BLM (1.00) CYP2D6CYP2C19KDM4EBLMNPSR1
Sulfuric Acid SCHEMBL29483831 0.83 BLM (0.94) CYP2D6CYP2C19KDM4EBLMNPSR1
Sulfuric Acid SCHEMBL21827141 0.80
SCHEMBL27962429 0.77 KDM4E (0.71) CYP2D6CYP2C19KDM4EBLMNPSR1
Ethylisothiourea SCHEMBL11693925 0.77 NOS1 (0.65) CYP2D6CYP2C19KDM4EBLMNPSR1
Bromide SCHEMBL27962443 0.76
Iodide SCHEMBL11696034 0.76
SCHEMBL78077 0.76

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12415828-B2 Modified oligonucleotides and methods for their synthesis NOOGEN LLC (RU) 2025-09-16 US disclosed
US-11596704-B2 Process monitoring device 3M INNOVATIVE PROPERTIES COMPANY (US) 2023-03-07 US disclosed
CN-115010780-A Modified oligonucleotide and preparation method thereof 努根有限责任公司 2022-09-06 CN disclosed
CN-106795197-B Modified oligonucleotide and preparation method thereof 努根有限责任公司 2022-06-28 CN disclosed
US-11208430-B2 Modified oligonucleotides and methods for their synthesis NOOGEN LLC (RU) 2021-12-28 US disclosed
EP-3904364-A1 MODIFIED OLIGONUCLEOTIDES AND METHODS FOR THEIR SYNTHESIS Noogen LLC (RU) 2021-11-03 EP disclosed
CN-112851663-A Fused heterocyclic compound and application thereof 博瑞生物医药(苏州)股份有限公司 2021-05-28 CN disclosed
CN-112745335-A Tri-heterocyclic compound and application thereof 武汉誉祥医药科技有限公司 2021-05-04 CN disclosed
EP-3183260-B1 MODIFIED OLIGONUCLEOTIDES AND METHODS FOR THEIR SYNTHESIS NOOGEN LLC (RU) 2021-03-31 EP disclosed
US-20210032283-A1 MODIFIED OLIGONUCLEOTIDES AND METHODS FOR THEIR SYNTHESIS WAVE LIFE SCIENCES LTD. (SG) 2021-02-04 US disclosed
US-7407965-B2 Phosphonate analogs for treating metabolic diseases GILEAD SCIENCES, INC. (US) 2008-08-05 US disclosed
US-7354895-B1 Phosphinyloxy, oxime and carboxylic acid derivatives which are useful as carboxypeptidase U inhibitors ASTRAZENECA AB (SE) 2008-04-08 US disclosed
US-20060079484-A1 Phosphinyloxy, oxime and carboxylic acid derivatives which are useful as carboxypeptidase U inhibitors LINSCHOTEN MARCEL 2006-04-13 US disclosed
US-20050227947-A1 Phosphonate analogs for treating metabolic diseases GILEAD SCIENCES, INC. 2005-10-13 US disclosed
WO-2004096237-A2 PHOSPHONATE ANALOGS FOR TREATING METABOLIC DISEASES GILEAD SCIENCES, INC. (US) 2004-11-11 WO disclosed
EP-1180099-A1 NEW COMPOUNDS AstraZeneca AB (SE) 2002-02-20 EP disclosed
WO-2000066550-A1 NEW COMPOUNDS ASTRAZENECA AB (SE) 2000-11-09 WO disclosed
US-5273989-A 3,5-disubstituted 2-isoxazolines and isoxazoles, agents containing them and their use HOECHST AKTIENGESELLSCHAFT (DE) 1993-12-28 US disclosed
US-5143915-A Hypotensive agents E. R. SQUIBB & SONS, INC. (US) 1992-09-01 US disclosed
US-4046884-A N-(α-Aminoalkylidene)phosphor- and phosphonamidates, and method for controlling insects VELSICOL CHEMICAL CORPORATION (US) 1977-09-06 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 (5 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-20210032283-A1 MODIFIED OLIGONUCLEOTIDES AND METHODS FOR THEIR SYNTHESIS RNGTT, TYMP, POLM CYP2D6 3987/4885CYP2C19 4782/4885KDM4E 3964/4885
US-12415828-B2 Modified oligonucleotides and methods for their synthesis RNGTT, TYMP, POLM CYP2D6 3987/4885CYP2C19 4782/4885KDM4E 3964/4885
US-20050227947-A1 Phosphonate analogs for treating metabolic diseases PHOSPHO1, G6PC1, PC CYP2D6 1991/4885CYP2C19 1676/4885KDM4E 2877/4885
US-11208430-B2 Modified oligonucleotides and methods for their synthesis TYMP, POLRMT, RNGTT CYP2D6 3261/4885CYP2C19 4042/4885KDM4E 4431/4885
US-20060079484-A1 Phosphinyloxy, oxime and carboxylic acid derivatives which are useful as carboxypeptidase U inhibitors CPN1, CPA1, DNPEP CYP2D6 736/4885CYP2C19 408/4885KDM4E 1165/4885

“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.