SCHEMBL3971438

SCHEMBL3971438

Cc1ccc(S(=O)(=O)N2CCN(S(=O)(=O)c3ccc(C)cc3)CCN(S(=O)(=O)c3ccc(C)cc3)CC2)cc1

nearest known ligand 0.88

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
PKM P14618 3/20 0.88
HTT P42858 2/20 0.88
ALDH1A1 P00352 2/20 0.88
POLB P06746 1/20 0.88
KMT2A Q03164 5/20 0.79
MEN1 O00255 3/20 0.79
GAA P10253 2/20 0.76
LMNA P02545 2/20 0.76
SMN1; SMN2 Q16637 1/20 0.76
TSHR P16473 1/20 0.72
CYP2C19 P33261 1/20 0.72
NPC1 O15118 1/20 0.67
RAB9A P51151 1/20 0.67

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
SCHEMBL3303527 1.00 PKM (0.88) PKMHTTALDH1A1POLBKMT2A
SCHEMBL699639 1.00 PKM (0.88) PKMHTTALDH1A1POLBKMT2A
SCHEMBL4537086 1.00 PKM (0.88) PKMHTTALDH1A1POLBKMT2A
SCHEMBL8200466 1.00 PKM (0.88) PKMHTTALDH1A1POLBKMT2A
SCHEMBL565301 1.00 PKM (0.88) PKMHTTALDH1A1POLBKMT2A
SCHEMBL8203532 1.00 PKM (0.88) PKMHTTALDH1A1POLBKMT2A
SCHEMBL10724066 1.00 PKM (0.88) PKMHTTALDH1A1POLBKMT2A
SCHEMBL8502340 0.94 PKM (1.00) PKMHTTALDH1A1POLBKMT2A
SCHEMBL8583228 0.94 PKM (1.00) PKMHTTALDH1A1POLBKMT2A
SCHEMBL7953663 0.94 PKM (1.00) PKMHTTALDH1A1POLBKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190276416-A1 METHOD FOR PREPARING NOTA DERIVATIVE Institute of Nuclear Energy Research, Atomic Energy Council, Executive Yuan, R.O.C. (TW) 2019-09-12 US claimed
US-5326861-A Cyclization LEVER BROTHERS COMPANY, DIVISION OF CONOPCO, INC. (US) 1994-07-05 US claimed
EP-3176155-B1 1,2-BIS-(4,7-DIMETHYL-1,4,7-TRIAZACYCLONON-1-YL)-ETHANE AND INTERMEDIATE FOR THE SYNTHESIS OF SAME CATEXEL LTD (GB) 2019-09-25 EP disclosed
US-20190276416-A1 METHOD FOR PREPARING NOTA DERIVATIVE Institute of Nuclear Energy Research, Atomic Energy Council, Executive Yuan, R.O.C. (TW) 2019-09-12 US disclosed
US-9988388-B2 Synthesis of imidazo[1,2-a]pyrazin-4-ium salts for the synthesis of 1,4,7-triazacyclononane (tacn) and N- and/or C- functionalized derivatives thereof UNIVERSITE DE BOURGOGNE (FR) 2018-06-05 US disclosed
US-9981967-B2 Synthesis of imidazo[1,2-a]pyrazin-4-ium salts for the synthesis of 1,4,7-triazacyclononane (tacn) and N- and/or C-functionalized derivatives thereof UNIVERSITE DE BOURGOGNE (FR) 2018-05-29 US disclosed
EP-3176155-A1 1,2-BIS-(4,7-DIMETHYL-1,4,7-TRIAZACYCLONON-1-YL)-ETHANE AND INTERMEDIATE FOR THE SYNTHESIS OF SAME Catexel Limited (GB) 2017-06-07 EP disclosed
EP-2590952-B1 1,2-BIS-(4,7-DIMETHYL-1,4,7-TRIAZACYCLONON-1-YL)-ETHANE AND INTERMEDIATE THEREOF CATEXEL LTD (GB) 2017-01-18 EP disclosed
US-20160222018-A1 SYNTHESIS OF IMIDAZO[1,2-a]PYRAZIN-4-IUM SALTS FOR THE SYNTHESIS OF 1,4,7-TRIAZACYCLONONANE (TACN) AND N- AND/OR C- FUNCTIONALIZED DERIVATIVES THEREOF UNIVERSITE DE BOURGOGNE (FR) 2016-08-04 US disclosed
US-20160222018-A1 SYNTHESIS OF IMIDAZO[1,2-a]PYRAZIN-4-IUM SALTS FOR THE SYNTHESIS OF 1,4,7-TRIAZACYCLONONANE (TACN) AND N- AND/OR C- FUNCTIONALIZED DERIVATIVES THEREOF UNIVERSITE DE BOURGOGNE (FR) 2016-08-04 US disclosed
CN-104529922-A Preparation method of 1,4,7-triazacyclononane hydrochloride SHENZHEN RES INST OF THE PHOTOGRAPHIC MATERIALS & CHEMICAL INDUSTRY 2015-04-22 CN disclosed
US-5874573-A Compounds with chelation affinity and selectivity for first transition series elements: use in medical therapy CONCAT, INC. (US) 1999-02-23 US disclosed
EP-0841951-A2 COMPOUNDS WITH CHELATION AFFINITY AND SELECTIVITY FOR FIRST TRANSITION SERIES ELEMENTS, AND THEIR USE IN MEDICAL THERAPY AND DIAGNOSIS CONCAT LTD. (US) 1998-05-20 EP disclosed
US-5739022-A CLEAVAGE PHOSPHORUS, OXYGEN LINKAGE FO NUCLEIC ACIDS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1998-04-14 US disclosed
WO-1997001360-A9 COMPOUNDS WITH CHELATION AFFINITY AND SELECTIVITY FOR FIRST TRANSITION SERIES ELEMENTS AND THEIR USE IN MEDICAL THERAPY AND DIAGNOSIS 1997-07-17 WO disclosed
WO-1997001360-A2 COMPOUNDS WITH CHELATION AFFINITY AND SELECTIVITY FOR FIRST TRANSITION SERIES ELEMENTS AND THEIR USE IN MEDICAL THERAPY AND DIAGNOSIS CONCAT, LTD. (US) 1997-01-16 WO disclosed
US-5326861-A Cyclization LEVER BROTHERS COMPANY, DIVISION OF CONOPCO, INC. (US) 1994-07-05 US disclosed
US-5326861-A Cyclization LEVER BROTHERS COMPANY, DIVISION OF CONOPCO, INC. (US) 1994-07-05 US disclosed
WO-1994008981-A1 PREPARATION OF ORGANIC MACROCYCLIC COMPOUNDS UNILEVER PLC (GB) 1994-04-28 WO disclosed
WO-1994008981-A1 PREPARATION OF ORGANIC MACROCYCLIC COMPOUNDS UNILEVER PLC (GB) 1994-04-28 WO 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-20160222018-A1 SYNTHESIS OF IMIDAZO[1,2-a]PYRAZIN-4-IUM SALTS FOR THE SYNTHESIS OF 1,4,7-TRIAZACYCLONONANE (TACN) AND N- AND/OR C- FUNCTIONALIZED DERIVATIVES THEREOF TAC3, TACR2, TACR3 PKM 627/4885HTT 2718/4885ALDH1A1 1366/4885

“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.