Tetrylammonium

Tetrylammonium

SCHEMBL36648

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

nearest known ligand 0.63

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRM1DRD2DRD3DRD4HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR2APDE3ASIGMAR1SLC9A3

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 13)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.42
NFKB1 P19838 3/20 0.42
KCNA1 Q09470 1/20 0.42
KDM4E B2RXH2 1/20 0.40
PMP22 Q01453 1/20 0.40
ATM Q13315 1/20 0.40
CYP3A4 P08684 2/20 0.39
NPSR1 Q6W5P4 2/20 0.39
CA1 P00915 3/20 0.38
TP53 P04637 1/20 0.36
CA4 P22748 2/20 0.35
CA2 P00918 1/20 0.35
SLC22A16 Q86VW1 1/20 0.34

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 SCHEMBL5573591 0.86 TSHR (0.44) TSHRNFKB1KCNA1KDM4EPMP22
L-Lactic Acid SCHEMBL5569772 0.84 SLC22A16 (0.44) TSHRNFKB1CYP3A4NPSR1CA1
Tetrylammonium SCHEMBL5874494 0.84 TSHR (0.42) TSHRNFKB1KCNA1KDM4EPMP22
Cadaverine Tartrate SCHEMBL5874349 0.84 TSHR (0.42) TSHRNFKB1KCNA1KDM4EPMP22
L-Lactic Acid SCHEMBL5573663 0.82 BBOX1 (0.45) TSHRNFKB1CYP3A4NPSR1CA1
Tetrylammonium SCHEMBL36649 0.81 TP53 (0.61) TSHRNFKB1KCNA1KDM4EPMP22
Tetrapropylammonium SCHEMBL5574321 0.80 SLC22A1 (0.48) TSHRNFKB1CYP3A4NPSR1CA1
Tetrylammonium SCHEMBL168440 0.80 TSHR (0.57) TSHRNFKB1KCNA1KDM4EPMP22
L-Lactic Acid SCHEMBL16585424 0.78 TSHR (0.42) TSHRNFKB1CYP3A4NPSR1CA1
L-Lactic Acid SCHEMBL7163760 0.78 TSHR (0.42) TSHRNFKB1CYP3A4NPSR1CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-115321585-B Indium hydroxide washing process 先导薄膜材料(安徽)有限公司 2023-08-11 CN claimed
CN-115321585-A Washing process of indium hydroxide 先导薄膜材料有限公司 2022-11-11 CN claimed
CN-111653767-B Washing process and preparation method of high-nickel polycrystalline ternary cathode material 乳源东阳光磁性材料有限公司 2021-10-01 CN claimed
CN-109876601-B Process method for absorbing sulfur dioxide in flue gas by functionalized ionic liquid and regenerating by Claus reaction at low temperature 北京化工大学 2020-10-02 CN claimed
CN-111653767-A Washing process and preparation method of high-nickel polycrystalline ternary cathode material 乳源东阳光磁性材料有限公司 2020-09-11 CN claimed
CN-110585860-A Low-energy-consumption regenerated absorbent and method for absorbing sulfur dioxide in flue gas by using same 太原师范学院 2019-12-20 CN claimed
CN-109876601-A A kind of functionalized ion liquid absorbing sulfur dioxide in flue and with the process of claus reaction low-temp recovery 北京化工大学 2019-06-14 CN claimed
CN-103079407-A Improved insecticidal compositions comprising cyclic carboximidamidines BAYER CROPSCIENCE AG 2013-05-01 CN claimed
US-20120004268-A1 INSECTICIDAL COMPOSITIONS COMPRISING CYCLIC CARBONYLAMIDINES BAYER CROPSCIENCE AG (DE) 2012-01-05 US claimed
CN-120118300-A Polycarbonate copolymer and preparation method and application thereof 华东理工大学 2025-06-10 CN disclosed
WO-2025000629-A1 PREPARATION METHOD FOR AND USE OF IONIC-LIQUID-MODIFIED CERIUM DIOXIDE CATALYST 中国科学院过程工程研究所 2025-01-02 WO disclosed
CN-116832859-B Preparation method and application of ionic liquid modified cerium oxide catalyst 中国科学院过程工程研究所 2024-12-03 CN disclosed
CN-118344595-A Polydimethylsiloxane-containing bio-based polycarbonate copolymer and preparation method thereof 中国科学院成都有机化学有限公司 2024-07-16 CN disclosed
US-20020133884-A1 Agents for treating synthetic fibers TAKEMOTO YUSHI KABUSHIKI KAISHA (JP) 2002-09-26 US disclosed
US-6432144-B1 Methods of treating synthetic fibers TAKEMOTO YUSHI KABUSHIKI KAISHA (JP) 2002-08-13 US disclosed
EP-1103651-A1 Agents for and methods of treating synthetic fibers Takemoto Yushi Kabushiki Kaisha (JP) 2001-05-30 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 (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-20120004268-A1 INSECTICIDAL COMPOSITIONS COMPRISING CYCLIC CARBONYLAMIDINES DDT, PRMT9, PNISR TSHR 2612/4885NFKB1 1573/4885KCNA1 380/4885

“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.