Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL331981

CC(O)C(=O)[O-].CCCC[N+](CCCC)(CCCC)CCCC

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRM1DRD2DRD3DRD4HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR2APDE3ASIGMAR1SLC9A3

The experimentally established mechanism targets of Tetrabuthylammonium. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
SLC22A1 O15245 3/20 0.52
CA1 P00915 2/20 0.52
SLC22A2 O15244 1/20 0.46
CA2 P00918 2/20 0.44
ALDH1A1 P00352 1/20 0.42
TP53 P04637 1/20 0.42
CYP3A4 P08684 1/20 0.42
ALOX15 P16050 1/20 0.42
TSHR P16473 1/20 0.42
ALOX12 P18054 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
HIF1A Q16665 1/20 0.42
HSD17B10 Q99714 1/20 0.42
NFKB1 P19838 1/20 0.41
CES2 O00748 1/20 0.41
CES1 P23141 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 SCHEMBL30104046 1.00 SLC22A1 (0.52) SLC22A1CA1SLC22A2CA2ALDH1A1
Tetrabuthylammonium SCHEMBL2398988 0.98 SLC22A1 (0.50) SLC22A1CA1SLC22A2CA2ALDH1A1
Tetrabuthylammonium SCHEMBL2398990 0.98 SLC22A1 (0.50) SLC22A1CA1SLC22A2CA2ALDH1A1
L-Lactic Acid SCHEMBL9630451 0.96 SLC22A1 (0.52) SLC22A1CA1SLC22A2CA2ALDH1A1
L-Lactic Acid SCHEMBL29256387 0.94 SLC22A1 (0.54) SLC22A1CA1SLC22A2CA2ALDH1A1
Tetrabuthylammonium SCHEMBL1691312 0.89 SLC22A1 (0.55) SLC22A1CA1SLC22A2CA2ALDH1A1
Tetrabuthylammonium SCHEMBL107578 0.87 SLC22A1 (0.52) SLC22A1CA1SLC22A2CA2ALDH1A1
Tetrabuthylammonium SCHEMBL5874496 0.87 SLC22A1 (0.52) SLC22A1CA1SLC22A2CA2ALDH1A1
Tetrapropylammonium SCHEMBL5574321 0.86 SLC22A1 (0.48) SLC22A1CA1CA2CYP3A4TSHR
Tetrabuthylammonium SCHEMBL31025702 0.85 SLC22A1 (0.50) SLC22A1CA1SLC22A2CA2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250314970-A1 OVERCOAT COMPOSITION AND PATTERNING METHODS TOKYO ELECTRON LTD (JP) 2025-10-09 US claimed
CN-118453443-A Use of vitamin C lactate and analogues thereof in preparation of skin tissue products and related products 长春圣博玛生物材料有限公司 2024-08-09 CN claimed
CN-117658802-A Method for preparing lactate by catalyzing alcoholysis of polylactic acid by ionic liquid 中国科学院化学研究所 2024-03-08 CN claimed
CN-117658794-A Method for preparing lactic acid by catalyzing polylactic acid hydrolysis through ionic liquid 中国科学院化学研究所 2024-03-08 CN claimed
CN-117623968-A Method for preparing N-substituted lactamide by catalyzing polylactic acid aminolysis with ionic liquid 中国科学院化学研究所 2024-03-01 CN claimed
CN-115951561-B Chemical amplification type positive I-line photoresist and preparation and use methods thereof 徐州博康信息化学品有限公司 2024-01-26 CN claimed
CN-117234034-A Photoresist and preparation and use methods thereof 江西兆驰半导体有限公司 2023-12-15 CN claimed
CN-115951561-A Chemically amplified positive I-line photoresist and preparation and use methods thereof 徐州博康信息化学品有限公司 2023-04-11 CN claimed
CN-1234047-C Chemical amplification light resistance agent compsn. AMERICAN EVERBRIGHT CORP (US) 2005-12-28 CN claimed
CN-1696829-A Chemically Amplified Photoresist Composition YONGGUANG CHEMICAL IND CO LTD (CN) 2005-11-16 CN claimed
US-6878504-B2 Chemically-amplified resist compositions EVERLIGHT USA, INC. (US) 2005-04-12 US claimed
US-20040241569-A1 Chemically-amplified resist compositions EVERLIGHT USA, INC. 2004-12-02 US claimed
CN-1538241-A Chemically Amplified Photoresist Composition 台湾永光化学工业股份有限公司 2004-10-20 CN claimed
US-6703178-B2 COMPRISES A POLYMER CONTAINING A NOVEL LACTONE ALICYCLIC UNIT; WELL-BALANCED OUTCOME OF ETCHING RESISTANCE AND SUBSTRATE ADHESION EVERLIGHT USA, INC. 2004-03-09 US claimed
CN-1462909-A Chemical amplification light resistance agent compsn. AMERICAN EVERBRIGHT CORP (US) 2003-12-24 CN claimed
US-20030232270-A1 CHEMICAL AMPLIFIED PHOTORESIST COMPOSITIONS EVERLIGHT USA, INC. (US) 2003-12-18 US claimed
US-12607933-B2 Polymer compositions having photoacid generators and photoresists DUPONT ELECTRONICS, INC. (US) 2026-04-21 US disclosed
US-12547072-B2 Self-aligned build-up processing GEMINATIO, INC. (US) 2026-02-10 US disclosed
EP-0783136-A2 Chemically amplified positive photoresists Shipley Company LLC (US) 1997-07-09 EP disclosed
US-5576459-A Quaternary nitrogen or phosphorus chirates SACHEM, INC. (US) 1996-11-19 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 (2 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-12547072-B2 Self-aligned build-up processing MYBBP1A, SMURF1, MYB SLC22A1 4459/4885CA1 1959/4885SLC22A2 4576/4885
US-12607933-B2 Polymer compositions having photoacid generators and photoresists PFAS, AFF1, HBG1 SLC22A1 2619/4885CA1 2237/4885SLC22A2 2884/4885

“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.