Tetrylammonium

Tetrylammonium

SCHEMBL36703

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

nearest known ligand 0.57

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

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 9)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.57
NFKB1 P19838 1/20 0.57
KCNA1 Q09470 1/20 0.57
KDM4E B2RXH2 1/20 0.53
PMP22 Q01453 1/20 0.53
ATM Q13315 1/20 0.53
BBOX1 O75936 3/20 0.39
TP53 P04637 1/20 0.33
DNM1 Q05193 2/20 0.30

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 SCHEMBL3643964 0.97 TSHR (0.53) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL621848 0.97 TSHR (0.53) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL28602156 0.97 TSHR (0.53) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL7638063 0.94 TSHR (0.50) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL5571612 0.91 TSHR (0.47) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL331297 0.90 TSHR (0.53) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL331443 0.90 TSHR (0.53) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL14118730 0.87 TSHR (0.50) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL36705 0.87 TSHR (0.50) TSHRNFKB1KCNA1KDM4EPMP22
Tetrylammonium SCHEMBL36659 0.87 TSHR (0.50) TSHRNFKB1KCNA1KDM4EPMP22

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122079721-A Method for converting C4-C5 isoparaffin 2026-05-26 CN claimed
CN-122079810-A Aromatic diamine and polyimide containing amido, preparation method and application thereof 2026-05-26 CN claimed
CN-122071633-A Stratum working fluid and system for viscosity reduction of thickened oil, and preparation method and application thereof 中国石油天然气股份有限公司 2026-05-22 CN claimed
CN-119308134-B Modified carbon fiber, carbon fiber reinforced composite coating, and preparation method and application thereof 中国科学院宁波材料技术与工程研究所 2026-05-19 CN claimed
CN-118515247-B High-stability organophosphorus functionalized black phosphorus nanosheet dispersion liquid and preparation method thereof 华南理工大学 2026-05-12 CN claimed
US-20260015560-A1 COMPOSITIONS FOR POST-CMP CLEANING OF MICROELECTRONIC DEVICES ENTEGRIS INC (US) 2026-01-15 US claimed
CN-119613418-A Dodecaurea cage type molecule, preparation method and application 北京理工大学 2025-03-14 CN claimed
CN-119308134-A Modified carbon fiber, carbon fiber reinforced composite coating, and preparation method and application thereof 中国科学院宁波材料技术与工程研究所 2025-01-14 CN claimed
CN-117700122-B Glass fiber impregnating compound and preparation method, product and application thereof 巨石集团有限公司 2024-09-27 CN claimed
CN-118515247-A High-stability organophosphorus functionalized black phosphorus nanosheet dispersion liquid and preparation method thereof 华南理工大学 2024-08-20 CN claimed
US-7176333-B2 Process for preparing 4-aminodiphenylamine SINORGCHEM COMPANY, SHANDONG (CN) 2007-02-13 US claimed
US-7084302-B2 reacting nitrobenzene and aniline in presence of condensation basic catalyst to form mixtures of 4-nitrodiphenylamine and 4-nitrosodiphenylamine, then reacting with hydrogen in the presence of hydrogenation catalysts, separation and refining SINORGCHEM SHANDONG CO., LTD. (CN) 2006-08-01 US claimed
EP-1645555-A1 A METHOD FOR PRODUCING 4-AMINODIPHENYLAMINE Shi, Guangqiang (CN) 2006-04-12 EP claimed
EP-1591438-A1 A PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE Wang, Nongyue (CN) 2005-11-02 EP claimed
US-20050240058-A1 reacting nitrobenzene and aniline in presence of condensation basic catalyst to form mixtures of 4-nitrodiphenylamine and 4-nitrosodiphenylamine, then reacting with hydrogen in the presence of hydrogenation catalysts, separation and refining NONGYUE WANG AND GUANGQIANG SHI (CN) 2005-10-27 US claimed
US-20050065376-A1 Process for preparing 4-aminodiphenylamine GUANGQIANG SHI AND NONGYUE WANG (CN) 2005-03-24 US claimed
CN-1460674-A Method for preparing tetraalkylammonium hydroxide QIANTANG SYNTHETIC NEW MATERIA (CN) 2003-12-10 CN claimed
US-4668349-A Acid promoted electrocatalytic reduction of carbon dioxide by square planar transition metal complexes THE STANDARD OIL COMPANY (US) 1987-05-26 US claimed
US-4522729-A CXONTACTING IMPORITIES WITH TETRAALKYLAMMONIUM SALT PHILLIPS PETROLEUM COMPANY (US) 1985-06-11 US claimed
US-3996078-A ALKANOLAMINE NITRATE OR PERCHLORATE DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1976-12-07 US 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-20260015560-A1 COMPOSITIONS FOR POST-CMP CLEANING OF MICROELECTRONIC DEVICES TET2, ASIC1, PIEZO1 TSHR 2647/4885NFKB1 2500/4885KCNA1 585/4885

“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.