Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL1250868

CCCC[N+](CCCC)(CCCC)CCCC.[H-]

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ SLC22A1 O15245 4/20 0.92
▸ SLC22A2 O15244 1/20 0.79
▸ TSHR P16473 2/20 0.69
▸ ALDH1A1 P00352 1/20 0.69
▸ TP53 P04637 1/20 0.69
▸ CYP3A4 P08684 1/20 0.69
▸ ALOX15 P16050 1/20 0.69
▸ ALOX12 P18054 1/20 0.69
▸ SMN1; SMN2 Q16637 1/20 0.69
▸ HIF1A Q16665 1/20 0.69
▸ HSD17B10 Q99714 1/20 0.69
▸ DNM1 Q05193 6/20 0.61

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
Tetrabuthylammonium SCHEMBL1800283 0.96 SLC22A1 (0.86) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL6622741 0.96 SLC22A1 (0.86) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL22384 0.96 SLC22A1 (1.00) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL71525 0.96 SLC22A1 (1.00) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL2007037 0.96 SLC22A1 (1.00) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL25266692 0.92 SLC22A1 (0.92) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL5069703 0.92 SLC22A1 (0.92) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL37663 0.92 SLC22A1 (0.92) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL4260120 0.92 SLC22A1 (0.92) SLC22A1SLC22A2TSHRALDH1A1TP53
Tetrabuthylammonium SCHEMBL7960336 0.92 SLC22A1 (0.92) SLC22A1SLC22A2TSHRALDH1A1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250215574-A1 SEMICONDUCTOR TREATMENT LIQUID FOR REMOVING RUTHENIUM SILICIDE TOKUYAMA CORPORATION (JP) 2025-07-03 — — US disclosed
EP-3395837-B1 CELLULOSE XANTHATE NANOFIBERS RENGO CO LTD (JP) 2021-12-15 — — EP disclosed
WO-2021075800-A1 METHOD FOR PREPARING WATER-SOLUBLE ACRYLIC-MODIFIED PHENOLIC-MODIFIED EPOXY RESIN, WATER-SOLUBLE ACRYLIC-MODIFIED PHENOLIC-MODIFIED EPOXY RESIN PREPARED THEREBY, AND AQUEOUS COATING COMPOSITION COMPRISING SAME 삼화페인트공업주식회사 2021-04-22 — — WO disclosed
WO-2020189665-A1 METHOD FOR PRODUCING VINYL POLYMER 株式会社カネカ 2020-09-24 — — WO disclosed
CN-111318303-A Phenolate and application thereof 中国科学院上海有机化学研究所 2020-06-23 — — CN disclosed
US-10662257-B2 Cellulose xanthate nanofiber RENGO CO., LTD. (JP) 2020-05-26 — — US disclosed
EP-3395837-A1 CELLULOSE XANTHATE NANOFIBERS Rengo Co., Ltd. (JP) 2018-10-31 — — EP disclosed
US-20180273644-A1 CELLULOSE XANTHATE NANOFIBER RENGO CO., LTD. (JP) 2018-09-27 — — US disclosed
US-9927697-B2 Mask blank, method of manufacturing mask blank and method of manufacturing transfer mask HOYA CORPORATION (JP) 2018-03-27 — — US disclosed
US-20160161844-A1 MASK BLANK, METHOD OF MANUFACTURING MASK BLANK AND METHOD OF MANUFACTURING TRANSFER MASK HOYA CORPORATION (JP) 2016-06-09 — — US disclosed
EP-0710223-A1 SYNTHESIS OF TAXOL AND ITS DERIVATIVES FLORIDA STATE UNIVERSITY (US) 1996-05-08 — — EP disclosed
EP-0681575-A4 — UNIV FLORIDA STATE (US) 1995-12-13 — — EP disclosed
EP-0681575-A1 PROCESS FOR THE PREPARATION OF BACCATIN III ANALOGS BEARING NEW C2 AND C4 FUNCTIONAL GROUPS FLORIDA STATE UNIVERSITY (US) 1995-11-15 — — EP disclosed
US-5405972-A Synthetic process for the preparation of taxol and other tricyclic and tetracyclic taxanes FLORIDA STATE UNIVERSITY (US) 1995-04-11 — — US disclosed
WO-1995003265-A1 SYNTHESIS OF TAXOL AND ITS DERIVATIVES FLORIDA STATE UNIVERSITY (US) 1995-02-02 — — WO disclosed
WO-1994017051-A1 PROCESS FOR THE PREPARATION OF BACCATIN III ANALOGS BEARING NEW C2 AND C4 FUNCTIONAL GROUPS FLORIDA STATE UNIVERSITY (US) 1994-08-04 — — WO disclosed
EP-0604969-A1 Low-resistance conductive pigment and method of manufacturing same MITSUBISHI MATERIALS CORPORATION (JP) 1994-07-06 — — EP disclosed
EP-0532759-A1 NOVEL ALLYL ALCOHOL DERIVATIVE TSUMURA & CO. (JP) 1993-03-24 — — EP disclosed
US-4895864-A FUNGICIDES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1990-01-23 — — US disclosed
EP-0289354-A2 Antibiotic TAN-950A, its production and use Takeda Chemical Industries, Ltd. (JP) 1988-11-02 — — EP disclosed
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