Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL7800475

CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.O=P([O-])([O-])F.O=P([O-])([O-])F.O=P([O-])([O-])F.O=P([O-])([O-])F

nearest known ligand 0.60

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC22A1 O15245 3/20 0.60
SLC22A2 O15244 1/20 0.52
ALDH1A1 P00352 1/20 0.48
TP53 P04637 1/20 0.48
CYP3A4 P08684 1/20 0.48
ALOX15 P16050 1/20 0.48
TSHR P16473 1/20 0.48
ALOX12 P18054 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
HIF1A Q16665 1/20 0.48
HSD17B10 Q99714 1/20 0.48
DNM1 Q05193 5/20 0.44
LMNA P02545 1/20 0.41
ESR1 P03372 1/20 0.41
ADORA3 P0DMS8 1/20 0.41
CDC25A P30304 1/20 0.41
AGTR1 P30556 1/20 0.41
AKT1 P31749 1/20 0.41
ADRA1A P35348 1/20 0.41
KCNH2 Q12809 1/20 0.41

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 SCHEMBL4652889 1.00 SLC22A1 (0.60) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL10933481 1.00 SLC22A1 (0.60) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL19834900 0.92 SLC22A1 (0.71) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL49814 0.92 SLC22A1 (0.71) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
SCHEMBL20543356 0.91 DNM1 (0.52) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL703752 0.90 SLC22A1 (0.67) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL31067882 0.90 SLC22A1 (0.67) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL28547695 0.90 SLC22A1 (0.67) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL3141779 0.90 SLC22A1 (0.67) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL28973535 0.90 SLC22A1 (0.67) SLC22A1SLC22A2ALDH1A1TP53CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119615197-A Electrochemical synthesis method of dichloro diphenyl silane 浙江大学 2025-03-14 CN claimed
CN-118619346-A Two-dimensional transition metal chalcogenide nanosheets and powder intercalation preparation method and application thereof 中国科学院化学研究所 2024-09-10 CN claimed
CN-115893491-A Sulfur vacancy rich tantalum sulfide nanosheet, preparation method thereof, sulfur vacancy rich tantalum sulfide nanosheet catalyst and application thereof 中国科学院化学研究所 2023-04-04 CN claimed
CN-114773226-B Method for preparing deuterated acetonitrile by photoelectricity integrated catalysis 安徽贵朋功能材料科技有限公司 2022-10-21 CN claimed
CN-114773226-A Method for preparing deuterated acetonitrile by photoelectric integrated catalysis 安徽贵朋功能材料科技有限公司 2022-07-22 CN claimed
US-20250204250-A1 NOVEL ORGANIC MONOMOLECULAR COMPOUND WITH MODIFIED ELECTRON TRANSPORT CHARACTERISTICS, AND DEVICE INCLUDING SAME PUKYONG NATIONAL UNIVERSITY INDUSTRY-UNIVERSITY COOPERATION FOUNDATION (KR) 2025-06-19 US disclosed
CN-119615197-A Electrochemical synthesis method of dichloro diphenyl silane 浙江大学 2025-03-14 CN disclosed
CN-112041970-B Aqueous composition and cleaning method using same 三菱瓦斯化学株式会社 2025-02-07 CN disclosed
CN-118619346-A Two-dimensional transition metal chalcogenide nanosheets and powder intercalation preparation method and application thereof 中国科学院化学研究所 2024-09-10 CN disclosed
CN-118547298-A Method for electrochemical reduction of aryl alkene and alkyne 中国科学院大连化学物理研究所 2024-08-27 CN disclosed
WO-2024091061-A1 DEVICE FOR THERMOAMPEROMETRY AND THERMOCOULOMETRY, AND ANALYSIS METHOD USING SAME 이화여자대학교 산학협력단 2024-05-02 WO disclosed
CN-117737754-A Method for electrocatalytic depolymerization of lignin and application thereof 南宁师范大学 2024-03-22 CN disclosed
CN-114773226-B Method for preparing deuterated acetonitrile by photoelectricity integrated catalysis 安徽贵朋功能材料科技有限公司 2022-10-21 CN disclosed
CN-114773226-A Method for preparing deuterated acetonitrile by photoelectric integrated catalysis 安徽贵朋功能材料科技有限公司 2022-07-22 CN disclosed
US-11352593-B2 Aqueous composition and cleaning method using same MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2022-06-07 US disclosed
US-20210155881-A1 AQUEOUS COMPOSITION AND CLEANING METHOD USING SAME MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2021-05-27 US disclosed
EP-3787010-A1 AQUEOUS COMPOSITION AND CLEANING METHOD USING SAME MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2021-03-03 EP disclosed
CN-112041970-A Aqueous composition and cleaning method using the same 三菱瓦斯化学株式会社 2020-12-04 CN disclosed
US-20010042693-A1 Electrical thick film HATHAWAY BROWN SCHOOL 2001-11-22 US disclosed
EP-0499638-B1 Method for Plating a Permanent Magnet of a R2T14B Intermetallic Compound TOKIN CORP (JP) 1998-12-02 EP 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 (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-20250204250-A1 NOVEL ORGANIC MONOMOLECULAR COMPOUND WITH MODIFIED ELECTRON TRANSPORT CHARACTERISTICS, AND DEVICE INCLUDING SAME SLCO2A1, SLCO4C1, SLCO2B1 SLC22A1 129/4885SLC22A2 226/4885ALDH1A1 562/4885

“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.