Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL769197

CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.O=P(O)(O)OP(=O)(O)O

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
SLC22A1 O15245 3/20 0.55
LPAR3 Q9UBY5 4/20 0.48
LPAR2 Q9HBW0 3/20 0.48
LPAR1 Q92633 2/20 0.48
SLC22A2 O15244 1/20 0.48
FDPS P14324 1/20 0.46
BLM P54132 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
ALDH1A1 P00352 1/20 0.44
TP53 P04637 1/20 0.44
CYP3A4 P08684 1/20 0.44
ALOX15 P16050 1/20 0.44
TSHR P16473 1/20 0.44
ALOX12 P18054 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
HIF1A Q16665 1/20 0.44
HSD17B10 Q99714 1/20 0.44
SMPD1 P17405 3/20 0.44

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 SCHEMBL21855087 1.00 SLC22A1 (0.55) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Tetrabuthylammonium SCHEMBL1577204 1.00 SLC22A1 (0.55) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Tetrabuthylammonium SCHEMBL21855085 0.98 SLC22A1 (0.52) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Tetrabuthylammonium SCHEMBL21631807 0.98 SLC22A1 (0.52) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Tetrabuthylammonium SCHEMBL21545821 0.98 SLC22A1 (0.52) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Tetrabuthylammonium SCHEMBL28421584 0.98 SLC22A1 (0.52) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Tetrabuthylammonium SCHEMBL9723905 0.91 SLC22A1 (0.50) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Tetrabuthylammonium SCHEMBL19834899 0.90 SLC22A1 (0.48) SLC22A1LPAR3LPAR2LPAR1SLC22A2
Pyrophosphoric Acid SCHEMBL27668809 0.88 FDPS (0.59) LPAR3LPAR2LPAR1FDPSBLM
Tetrabuthylammonium SCHEMBL21496366 0.88 SLC22A1 (0.46) SLC22A1LPAR3LPAR2LPAR1SLC22A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4741406-A1 NEUROKININ-1 RECEPTOR ANTAGONIST COMPOUND Creadev (Nanjing) Pharmaceutical Technology Co., Ltd. (CN) 2026-05-13 EP disclosed
US-12522630-B2 MRNA cap analog and uses thereof HANMI FINE CHEMICAL CO., LTD. (KR) 2026-01-13 US disclosed
US-20250257090-A1 Ribonucleic Acids With 4'-Thio-Modified Nucleotides and Related Methods TRANSLATE BIO, INC. (US) 2025-08-14 US disclosed
US-20250230183-A1 MRNA CAP ANALOG AND USES THEREOF HANMI FINE CHEMICAL CO., LTD. (KR) 2025-07-17 US disclosed
WO-2025149479-A1 SYNTHESIS OF MODIFIED NUCLEOSIDE TRIPHOSPHATES ROCHE DIAGNOSTICS GMBH (DE) 2025-07-17 WO disclosed
US-20250197820-A1 NUCLEIC ACID POLYMERASE AND ITS USE IN PRODUCING NON-DNA NUCLEOTIDE POLYMERS UNITED KINGDOM RESEARCH AND INNOVATION (GB) 2025-06-19 US disclosed
WO-2025071359-A1 MRNA CAP ANALOG AND USE THEREOF 한미정밀화학 주식회사 2025-04-03 WO disclosed
EP-4506353-A1 MRNA CAP ANALOG AND USES THEREOF Hanmi Fine Chemical Co., Ltd. (KR) 2025-02-12 EP disclosed
US-20240327444-A1 Method for Purifying Nucleotides, Device for Purifying Nucleotides, Hy-Drophobic Reagent, and Hydrophobic Substrate JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2024-10-03 US disclosed
EP-4399285-A2 NUCLEIC ACID POLYMERASE AND ITS USE IN PRODUCING NON-DNA NUCLEOTIDE POLYMERS United Kingdom Research and Innovation (GB) 2024-07-17 EP disclosed
EP-1263752-A4 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE UNIV TENNESSEE RES CORP (US) 2003-07-30 EP disclosed
US-20030130237-A1 LPA receptor agonists and antagonists and methods of use MILLER DUANE D (US) 2003-07-10 US disclosed
US-6586461-B1 Geranylgeranyl transferase inhibitors comprising farnesol and geranylgeraniol analogs, used as anticarcinogenic agents and for prevention of restenosis WAYNE STATE UNIVERSITY 2003-07-01 US disclosed
WO-2003024402-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2003-03-27 WO disclosed
US-20030027800-A1 LPA receptor agonists and antagonists and methods of use NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2003-02-06 US disclosed
EP-1263752-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2002-12-11 EP disclosed
WO-2002083720-A2 INTERMEDIATES AND ENZYMES OF THE NON-MEVALONATE ISOPRENOID PATHWAY BACHER ADELBERT (DE) 2002-10-24 WO disclosed
WO-2001071022-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2001-09-27 WO disclosed
US-6284910-B1 FARNESYL TRANSFERASE INHIBITORS UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION 2001-09-04 US disclosed
US-5668171-A Halogenated mevalonate compositions and uses thereof in ras-dependent cell growth BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1997-09-16 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-20250257090-A1 Ribonucleic Acids With 4'-Thio-Modified Nucleotides and Related Methods RNMT, RNGTT, NSUN3 SLC22A1 2481/4885LPAR3 3252/4885LPAR2 3172/4885
US-20250230183-A1 MRNA CAP ANALOG AND USES THEREOF RNGTT, RNMT, CAP1 SLC22A1 2501/4885LPAR3 4202/4885LPAR2 4358/4885
US-20030027800-A1 LPA receptor agonists and antagonists and methods of use LPAR1, LPAR2, LPAR3 SLC22A1 2861/4885LPAR3 3/4885LPAR2 2/4885
US-20240327444-A1 Method for Purifying Nucleotides, Device for Purifying Nucleotides, Hy-Drophobic Reagent, and Hydrophobic Substrate NUDT1, SAMHD1, PNP SLC22A1 1221/4885LPAR3 2353/4885LPAR2 2782/4885
US-20030130237-A1 LPA receptor agonists and antagonists and methods of use LPAR1, LPAR2, LPAR5 SLC22A1 3374/4885LPAR3 4/4885LPAR2 2/4885

“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.