Tetrylammonium

Tetrylammonium

SCHEMBL5374883

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nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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 9)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 1.00
PMP22 Q01453 1/20 1.00
ATM Q13315 1/20 1.00
TSHR P16473 2/20 0.89
NFKB1 P19838 1/20 0.89
KCNA1 Q09470 1/20 0.89
DNM1 Q05193 4/20 0.39
SLC22A1 O15245 3/20 0.36
SLC22A2 O15244 1/20 0.31

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 SCHEMBL10982449 1.00 KDM4E (1.00) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL49847 1.00 KDM4E (1.00) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL9183225 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL6560332 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL11589433 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL9183233 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL5374887 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL228998 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL22664597 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1
Tetrylammonium SCHEMBL9183220 0.95 KDM4E (0.90) KDM4EPMP22ATMTSHRNFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250188006-A1 13C-LABELLED CHLORINATED PARAFFINS AND THEIR PREPARATION CHIRON AS (NO) 2025-06-12 US claimed
EP-4493530-A1 13 C-LABELLED CHLORINATED PARAFFINS AND THEIR PREPARATION Chiron AS (NO) 2025-01-22 EP claimed
WO-2023174709-A1 13C-LABELLED CHLORINATED PARAFFINS AND THEIR PREPARATION CHIRON AS (NO) 2023-09-21 WO claimed
EP-4245742-A1 13C-LABELLED CHLORINATED PARAFFINS AND THEIR PREPARATION Chiron AS (NO) 2023-09-20 EP claimed
US-3997362-A AMMONIUM EXXON RESEARCH AND ENGINEERING COMPANY (US) 1976-12-14 US claimed
EP-3507316-B1 HALOGEN AND POLYHALIDE MEDIATED PHENOLIC POLYMERIZATION 3M INNOVATIVE PROPERTIES COMPANY (US) 2026-02-11 EP disclosed
EP-4617325-A1 QUINACRIDONE COMPOUND DIC Corporation (JP) 2025-09-17 EP disclosed
EP-4617326-A1 DIKETOPYRROLOPYRROLE COMPOUND DIC Corporation (JP) 2025-09-17 EP disclosed
US-20250188006-A1 13C-LABELLED CHLORINATED PARAFFINS AND THEIR PREPARATION CHIRON AS (NO) 2025-06-12 US disclosed
CN-119907833-A Pyrrolopyrroldione compounds DIC株式会社 2025-04-29 CN disclosed
CN-119604587-A Quinacridone compounds DIC株式会社 2025-03-11 CN disclosed
EP-4493530-A1 13 C-LABELLED CHLORINATED PARAFFINS AND THEIR PREPARATION Chiron AS (NO) 2025-01-22 EP disclosed
US-6528664-B2 Synthetic methods for polyphenols MARS, INCORPORATED 2003-03-04 US disclosed
EP-1027345-B1 SYNTHETIC METHODS FOR POLYPHENOLS MARS INC (US) 2003-02-19 EP disclosed
US-20020128493-A1 Coupling flavonoid-like compounds having protected hydroxy groups by functionalizing the C-4; oxidative dehydrogenation to form dimers and oligomers; efficiency; anticarciogenic agents; breast cancer MARS, INCORPORATED 2002-09-12 US disclosed
US-6420572-B1 FLAVANOID DERIVATIVES AND PHENOLIC DERIVATIVES WITH HALOGENATION MARS, INCORPORATED 2002-07-16 US disclosed
US-6242609-B1 AMMONIUM TRIHALIDE FOR HALOGENATION OF COLOR COUPLERS AND SILVER HALIDE EMULSIONS KONICA CORPORATION (JP) 2001-06-05 US disclosed
EP-1027345-A1 SYNTHETIC METHODS FOR POLYPHENOLS Mars Incorporated (US) 2000-08-16 EP disclosed
WO-1999019319-A1 SYNTHETIC METHODS FOR POLYPHENOLS MARS INCORPORATED (US) 1999-04-22 WO disclosed
US-3997362-A AMMONIUM EXXON RESEARCH AND ENGINEERING COMPANY (US) 1976-12-14 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-20020128493-A1 Coupling flavonoid-like compounds having protected hydroxy groups by functionalizing the C-4; oxidative dehydrogenation to form dimers and oligomers; efficiency; anticarciogenic agents; breast cancer GPX4, NOX4, TPD52L2 KDM4E 1217/4885PMP22 4726/4885ATM 4487/4885
US-20250188006-A1 13C-LABELLED CHLORINATED PARAFFINS AND THEIR PREPARATION PCNA, CAT, CDC73 KDM4E 785/4885PMP22 289/4885ATM 2328/4885

“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.