Tetrylammonium

Tetrylammonium

SCHEMBL160282

CC[N+](CC)(CC)CC.Cc1ccc(S(=O)(=O)[O-])cc1

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRM1CHRM2CHRM3CHRM4CHRM5SLC6A2dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Tetrylammonium. 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
LMNA P02545 3/20 0.53
CYP2D6 P10635 2/20 0.53
CYP3A4 P08684 2/20 0.53
MAPK1 P28482 1/20 0.53
THPO P40225 1/20 0.53
KCNH2 Q12809 2/20 0.52
CYP2C9 P11712 2/20 0.52
CYP2C19 P33261 2/20 0.52
TSHR P16473 1/20 0.52
HTT P42858 1/20 0.52
HIF1A Q16665 1/20 0.52
GAA P10253 2/20 0.48
ALDH1A1 P00352 4/20 0.47
G6PD P11413 2/20 0.46
CA2 P00918 3/20 0.45
CA1 P00915 2/20 0.45
CA12 O43570 2/20 0.45
CA9 Q16790 2/20 0.45
CA3 P07451 1/20 0.45
CA6 P23280 1/20 0.45

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
Tetrylammonium SCHEMBL9476357 0.98 LMNA (0.51) LMNACYP2D6CYP3A4MAPK1THPO
Tetrylammonium SCHEMBL3637947 0.94 LMNA (0.52) LMNACYP2D6CYP3A4MAPK1THPO
SCHEMBL23754813 0.89 LMNA (0.58) LMNACYP2D6CYP3A4MAPK1THPO
SCHEMBL8505186 0.86 LMNA (0.55) LMNACYP2D6CYP3A4MAPK1THPO
SCHEMBL2942432 0.86 LMNA (0.62) LMNACYP2D6CYP3A4MAPK1THPO
SCHEMBL4660154 0.84 KCNH2 (0.47) LMNACYP2D6CYP3A4MAPK1THPO
Tetrapropylammonium SCHEMBL330672 0.84 CYP2D6 (0.53) LMNACYP2D6CYP3A4MAPK1THPO
Tetrylammonium SCHEMBL1815475 0.83 PSIP1 (0.50) LMNACYP2D6CYP3A4MAPK1THPO
SCHEMBL330892 0.83 LMNA (0.53) LMNACYP2D6CYP3A4MAPK1THPO
SCHEMBL330725 0.83 KCNH2 (0.70) LMNACYP2D6CYP3A4MAPK1THPO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025233841-A1 ELECTROCHEMICAL OXIDATION OF 1,2-CYCLOHEXANEDIOL INV NYLON CHEMICALS AMERICAS, LLC (US) 2025-11-13 WO claimed
US-20250296952-A1 METHOD FOR PREPARING ABIRATERONE ACETATE AND INTERMEDIATE THEREOF AURISCO PHARMACEUTICAL CO., LTD. (CN) 2025-09-25 US claimed
CN-120060868-A Preparation method of 6-azaspiro [2.5] octane-6-carboxylic acid-1, 1-dimethylethyl ester 南京药石科技股份有限公司 2025-05-30 CN claimed
CN-119876972-A Electrochemical synthesis method of 4' -N-methyl benzyl-3-indole derivative 深圳职业技术大学 2025-04-25 CN claimed
CN-117185976-B Synthesis method of compound L635 深圳市灵兰生物医药科技有限公司 2024-12-31 CN claimed
EP-4464696-A1 CHEMICALLY DEGRADABLE EPOXY COMPOUND, METHOD FOR PREPARING SAME, EPOXY COMPOSITE MATERIAL COMPRISING SAME, AND DECOMPOSITION METHOD THEREOF Konkuk University Industrial Cooperation Corp. (KR) 2024-11-20 EP claimed
CN-117304123-B Preparation method of sun-screening agent Tianlai S 安徽圣诺贝化学科技有限公司 2024-10-01 CN claimed
CN-117385378-B Electrooxidation preparation method and application of electron-deficient aromatic acetal 厦门大学 2024-09-24 CN claimed
CN-118048633-A Method for electrochemically synthesizing trifluoro methylthio oxindole 上海电力大学 2024-05-17 CN claimed
CN-117816238-A Polyethylene nanofiber supported gold-ionic liquid catalyst for catalyzing hydrochlorination of acetylene as well as preparation and application thereof 浙江工业大学 2024-04-05 CN claimed
US-4929316-A Method of manufacturing organic semi-conductor solid electrolytic capacitor NIKSUKO CORPORATION (JP) 1990-05-29 US claimed
US-4929389-A POLYPYRROLES, POLYTHIOPHENES, ANISOTROPIC POLYMERS THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF ENERGY (US) 1990-05-29 US claimed
US-4880508-A Water-soluble conductive polymers THE UNITED STATES OF AMERICA AS REPRESENTED BY THE UNITED STATES DEPARTMENT OF ENERGY (US) 1989-11-14 US claimed
WO-1989007957-A1 CO2 INDICATOR FOR PLACEMENT OF TRACHEAL TUBES BRIGHAM AND WOMEN'S HOSPITAL (US) 1989-09-08 WO claimed
US-4457810-A ANODIC OXIDATION OF DI-P-TOLYL ETHER IN PRESENCE OF METHANOL HOECHST AKTIENGESELLSCHAFT (DE) 1984-07-03 US claimed
EP-0054698-B1 4,4'-DIPHENYL ETHER-DIALDEHYDE-BIS-DIMETHYL ACETAL, AND A METHOD FOR ITS PREPARATION HOECHST AKTIENGESELLSCHAFT (DE) 1984-06-20 EP claimed
US-4399007-A APPLYING POTENTIAL, CATALYST SELECTIVITY LEVER BROTHERS COMPANY (US) 1983-08-16 US claimed
EP-0017907-B1 PROCESS FOR PRODUCING CYCLOHEXENE DERIVATIVES F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1983-02-09 EP claimed
EP-0054698-A1 4,4'-Diphenyl ether-dialdehyde-bis-dimethyl acetal, and a method for its preparation HOECHST AKTIENGESELLSCHAFT (DE) 1982-06-30 EP claimed
EP-0017907-A1 Process for producing cyclohexene derivatives F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1980-10-29 EP claimed

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-20250296952-A1 METHOD FOR PREPARING ABIRATERONE ACETATE AND INTERMEDIATE THEREOF CYP17A1, CYP21A2, CYP19A1 LMNA 2133/4885CYP2D6 91/4885CYP3A4 48/4885

“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.