SCHEMBL422343

SCHEMBL422343

NCCCCCCN(CCO)CCO

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 1/20 0.46
DNM1 Q05193 4/20 0.42
CA12 O43570 2/20 0.42
CA1 P00915 2/20 0.42
CA2 P00918 2/20 0.42
CA3 P07451 2/20 0.42
CA4 P22748 2/20 0.42
CA6 P23280 2/20 0.42
CA5A P35218 2/20 0.42
CA7 P43166 2/20 0.42
CA9 Q16790 2/20 0.42
CA14 Q9ULX7 2/20 0.42
CA5B Q9Y2D0 2/20 0.42
TSHR P16473 2/20 0.42
LMNA P02545 2/20 0.42
BLM P54132 1/20 0.42
NFKB1 P19838 1/20 0.37
ALDH1A1 P00352 2/20 0.35
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33

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
SCHEMBL7523529 1.00 CHRM2 (0.46) CHRM2DNM1CA12CA1CA2
SCHEMBL29837911 1.00 CHRM2 (0.46) CHRM2DNM1CA12CA1CA2
SCHEMBL9190540 1.00 CHRM2 (0.46) CHRM2DNM1CA12CA1CA2
SCHEMBL29198096 0.97 CHRM2 (0.42) CHRM2DNM1CA12CA1CA2
SCHEMBL3077794 0.97 CHRM2 (0.42) CHRM2DNM1CA12CA1CA2
SCHEMBL30186917 0.95 CHRM2 (0.40) CHRM2DNM1CA12CA1CA2
Trolamine SCHEMBL28176957 0.95 DNM1 (0.47) CHRM2DNM1CA12CA1CA2
SCHEMBL28333383 0.90 CHRM2 (0.46) CHRM2DNM1CA12CA1CA2
SCHEMBL1674639 0.89 TSHR (0.39) CHRM2DNM1CA12CA1CA2
SCHEMBL11591877 0.89 TSHR (0.39) CHRM2DNM1CA12CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3390344-B1 IMPROVED METHOD FOR SYNTHESISING PARTIALLY N-HYDROXYETHYLATED TERTIARY 1,6-HEXANEDIAMINES IFP ENERGIES NOW (FR) 2020-12-02 EP claimed
US-10618866-B2 Method for synthesising partially N-hydroxyethylated tertiary 1,6-hexanediamines IFP Energies Nouvelles (FR) 2020-04-14 US claimed
US-20190002392-A1 IMPROVED METHOD FOR SYNTHESISING PARTIALLY N-HYDROXYETHYLATED TERTIARY 1,6-HEXANEDIAMINES IFP Energies Nouvelles (FR) 2019-01-03 US claimed
EP-4644507-A1 RUBBER COMPOSITION FOR SEAL MATERIAL VALQUA, Ltd. (JP) 2025-11-05 EP disclosed
US-20250109277-A1 CYCLIC OLEFIN RESIN COMPOSITION, MOLDED ARTICLE, AND OPTICAL COMPONENT MITSUI CHEMICALS, INC. (JP) 2025-04-03 US disclosed
WO-2024142767-A1 RUBBER COMPOSITION FOR SEAL MATERIAL 株式会社バルカー 2024-07-04 WO disclosed
WO-2023153302-A1 CYCLIC OLEFIN RESIN COMPOSITION, MOLDED ARTICLE AND OPTICAL COMPONENT 三井化学株式会社 2023-08-17 WO disclosed
US-10967325-B2 Absorbent solution based on hydroxyl derivatives of 1,6-hexanediamine and method for eliminating acid compounds from a gaseous effluent IFP Energies Nouvelles (FR) 2021-04-06 US disclosed
EP-3390344-B1 IMPROVED METHOD FOR SYNTHESISING PARTIALLY N-HYDROXYETHYLATED TERTIARY 1,6-HEXANEDIAMINES IFP ENERGIES NOW (FR) 2020-12-02 EP disclosed
US-20200323889-A1 CYCLODEXTRIN-BASED POLYMERS FOR THERAPEUTIC DELIVERY CERULEAN PHARMA INC. 2020-10-15 US disclosed
US-20200254380-A1 ABSORBENT SOLUTION BASED ON HYDROXYL DERIVATIVES OF 1,6-HEXANEDIAMINE AND METHOD FOR ELIMINATING ACID COMPOUNDS FROM A GASEOUS EFFLUENT IFP Energies Nouvelles (FR) 2020-08-13 US disclosed
US-20020182581-A1 Treating blood or blood products with compounds which have a mustard, aziridinium or aziridine group and a nucleic acid binding group CERUS CORPORATION (US) 2002-12-05 US disclosed
US-6410219-B1 DECTIONN OF PATHOGEN DEACTION OF PATHOGEN BY COMPLEXING CERUS CORPORATION 2002-06-25 US disclosed
US-6171777-B1 DECONTAMINATING BY CONTACTING WITH COMPOUND, THEN RECOVERING PRODUCT; DEACTIVATES HUMAN IMMUNODEFICIENCY AND HEPATITIS VIRUSES; BEFORE TRANSFUSIONS OR CLINICAL TESTS CERUS CORPORATION 2001-01-09 US disclosed
US-6143490-A IN VITRO METHOD FOR DEACTIVATION OF VIRAL, BACTERIAL, OR PROTOZOAN PATHOGEN BY ADDING COMPOUND CONSISTING OF INTERCALATOR NUCLEIC ACID BINDING LIGAND AND AN ATTACHED MUSTARD GROUP, TREATING THE MIXTURE, AND RECOVERING BLOOD CERUS CORPORATION (US) 2000-11-07 US disclosed
EP-0773716-A4 TREATING RED BLOOD CELL SOLUTIONS WITH ANTI-VIRAL AGENTS CERUS CORP (US) 1999-08-04 EP disclosed
EP-0888283-A1 WIDELY-BRIDGED ALCOHOL POLYETHOXYLATES AND THEIR USE ALBEMARLE CORPORATION (US) 1999-01-07 EP disclosed
WO-1998014422-A1 WIDELY-BRIDGED ALCOHOL POLYETHOXYLATES AND THEIR USE ALBEMARLE CORPORATION (US) 1998-04-09 WO disclosed
EP-0773716-A1 TREATING RED BLOOD CELL SOLUTIONS WITH ANTI-VIRAL AGENTS Cerus Corporation (US) 1997-05-21 EP disclosed
WO-1996039818-A1 TREATING RED BLOOD CELL SOLUTIONS WITH ANTI-VIRAL AGENTS CERUS CORPORATION (US) 1996-12-19 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 (6 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-20190002392-A1 IMPROVED METHOD FOR SYNTHESISING PARTIALLY N-HYDROXYETHYLATED TERTIARY 1,6-HEXANEDIAMINES BHMT2, DNMT1, DNMT3A CHRM2 490/4885DNM1 2488/4885CA12 4587/4885
US-20020182581-A1 Treating blood or blood products with compounds which have a mustard, aziridinium or aziridine group and a nucleic acid binding group ADAR, CD99, AAAS CHRM2 4623/4885DNM1 3633/4885CA12 1068/4885
US-10967325-B2 Absorbent solution based on hydroxyl derivatives of 1,6-hexanediamine and method for eliminating acid compounds from a gaseous effluent HAAO, HPD, ALKBH1 CHRM2 122/4885DNM1 2420/4885CA12 2445/4885
US-20200254380-A1 ABSORBENT SOLUTION BASED ON HYDROXYL DERIVATIVES OF 1,6-HEXANEDIAMINE AND METHOD FOR ELIMINATING ACID COMPOUNDS FROM A GASEOUS EFFLUENT HAAO, HPD, ALKBH1 CHRM2 122/4885DNM1 2420/4885CA12 2445/4885
US-10618866-B2 Method for synthesising partially N-hydroxyethylated tertiary 1,6-hexanediamines BHMT2, DNMT1, HNMT CHRM2 489/4885DNM1 2507/4885CA12 4574/4885
US-20200323889-A1 CYCLODEXTRIN-BASED POLYMERS FOR THERAPEUTIC DELIVERY PSMG3, COPB1, PSMA6 CHRM2 4714/4885DNM1 2474/4885CA12 1452/4885

“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.