Tetrylammonium

Tetrylammonium

SCHEMBL331006

CCCCCCCCCCCCc1ccccc1S(=O)(=O)[O-].CC[N+](CC)(CC)CC

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LIPG Q9Y5X9 1/20 0.47
KCNH2 Q12809 7/20 0.43
LMNA P02545 1/20 0.43
CYP2D6 P10635 1/20 0.43
CYP2C9 P11712 1/20 0.43
TSHR P16473 1/20 0.43
CYP2C19 P33261 1/20 0.43
HTT P42858 1/20 0.43
HIF1A Q16665 1/20 0.43
NR1H2 P55055 1/20 0.40
NR1H3 Q13133 1/20 0.40
CYSLTR2 Q9NS75 5/20 0.40
CYSLTR1 Q9Y271 5/20 0.40
BID P55957 3/20 0.38
MCL1 Q07820 3/20 0.38
BCL2L1 Q07817 2/20 0.38
BAK1 Q16611 2/20 0.38

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
SCHEMBL331384 0.93 KCNH2 (0.48) LIPGKCNH2LMNACYP2D6CYP2C9
SCHEMBL330871 0.93 KCNH2 (0.48) LIPGKCNH2LMNACYP2D6CYP2C9
SCHEMBL16895142 0.92 LIPG (0.54) LIPGKCNH2NR1H2NR1H3CYSLTR2
Tetrabuthylammonium SCHEMBL330368 0.91 LIPG (0.47) LIPGKCNH2LMNACYP2D6CYP2C9
SCHEMBL331308 0.91 LIPG (0.47) LIPGKCNH2LMNACYP2D6CYP2C9
Tetrahexylammonium SCHEMBL331148 0.91 LIPG (0.47) LIPGKCNH2LMNACYP2D6CYP2C9
Tetramethylammonium Ion SCHEMBL330911 0.91 LIPG (0.50) LIPGKCNH2NR1H2NR1H3CYSLTR2
Potassium Ion SCHEMBL23749193 0.91 LIPG (0.53) LIPGKCNH2NR1H2NR1H3CYSLTR2
Lithium Ion SCHEMBL21822090 0.91 LIPG (0.53) LIPGKCNH2NR1H2NR1H3CYSLTR2
Lithium Ion SCHEMBL21822174 0.91 LIPG (0.53) LIPGKCNH2NR1H2NR1H3CYSLTR2

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9920020-B2 Using squaraine dyes as near infrared fluorescent sensors for protein detection THE UNIVERSITY OF AKRON (US) 2018-03-20 US claimed
US-20120276642-A1 USING SQUARAINE DYES AS NEAR INFRARED FLUORESCENT SENSORS FOR PROTEIN DETECTION THE UNIVERSITY OF AKRON 2012-11-01 US claimed
US-9920020-B2 Using squaraine dyes as near infrared fluorescent sensors for protein detection THE UNIVERSITY OF AKRON (US) 2018-03-20 US disclosed
EP-2295484-B1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM SAME POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS INC (JP) 2018-01-17 EP disclosed
EP-2407498-B1 Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material MITSUI CHEMICALS INC (JP) 2017-11-15 EP disclosed
US-20170107401-A1 METHOD FOR APPLYING HIGH PERFORMANCE SILICON-BASED COATING COMPOSITIONS BURNING BUSH GROUP, LLC (US) 2017-04-20 US disclosed
EP-2958966-A2 METHOD FOR APPLYING HIGH PERFORMANCE SILICON-BASED COATING COMPOSITIONS Burning Bush Group, LLC (US) 2015-12-30 EP disclosed
WO-2014130774-A2 METHOD FOR APPLYING HIGH PERFORMANCE SILICON-BASED COATING COMPOSITIONS Burning Bush Technologies, LLC (US) 2014-08-28 WO disclosed
US-20140234534-A1 METHOD FOR APPLYING HIGH PERFORMANCE SILICON-BASED COATING COMPOSITIONS Burning Bush Technologies, LLC (US) 2014-08-21 US disclosed
US-8304507-B2 Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material MITSUI CHEMICALS, INC. (JP) 2012-11-06 US disclosed
US-20120276642-A1 USING SQUARAINE DYES AS NEAR INFRARED FLUORESCENT SENSORS FOR PROTEIN DETECTION THE UNIVERSITY OF AKRON 2012-11-01 US disclosed
EP-2407498-A2 Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material Mitsui Chemicals, Inc. (JP) 2012-01-18 EP disclosed
US-20110112269-A1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM THE POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS, INC. (JP) 2011-05-12 US disclosed
EP-2295484-A1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM SAME POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL Mitsui Chemicals, Inc. (JP) 2011-03-16 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-20120276642-A1 USING SQUARAINE DYES AS NEAR INFRARED FLUORESCENT SENSORS FOR PROTEIN DETECTION SPR, IK, SPAST LIPG 3536/4885KCNH2 2929/4885LMNA 3123/4885

“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.