SCHEMBL4001682

SCHEMBL4001682

NCCOCCCCOCCN

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ODC1 P11926 1/20 0.37
NFKB1 P19838 1/20 0.33
HTT P42858 2/20 0.32
MEN1 O00255 1/20 0.32
THRB P10828 1/20 0.32
KMT2A Q03164 1/20 0.32
MAPT P10636 1/20 0.32
CA12 O43570 2/20 0.31
CA1 P00915 2/20 0.31
CA2 P00918 2/20 0.31
CA3 P07451 2/20 0.31
CA4 P22748 2/20 0.31
CA6 P23280 2/20 0.31
CA5A P35218 2/20 0.31
CA7 P43166 2/20 0.31
CA9 Q16790 2/20 0.31
CA14 Q9ULX7 2/20 0.31
CA5B Q9Y2D0 2/20 0.31
TSHR P16473 2/20 0.31
DNM1 Q05193 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
SCHEMBL16353341 0.96 MEN1 (0.36) ODC1NFKB1HTTMEN1THRB
SCHEMBL3998325 0.96 CA1 (0.38) ODC1NFKB1HTTMEN1THRB
SCHEMBL18902842 0.96 CA1 (0.38) ODC1NFKB1HTTMEN1THRB
SCHEMBL3996449 0.96 CA1 (0.38) ODC1NFKB1HTTMEN1THRB
SCHEMBL24870864 0.93 HTT (0.40) ODC1HTTMEN1THRBKMT2A
SCHEMBL10796626 0.93 ODC1 (0.47) ODC1NFKB1CA12CA1CA2
SCHEMBL6826021 0.93
SCHEMBL3292227 0.92 ODC1 (0.37) ODC1NFKB1CA12CA1CA2
SCHEMBL12918856 0.92 ODC1 (0.37) ODC1NFKB1CA12CA1CA2
SCHEMBL23193800 0.90 DNM1 (0.50) ODC1NFKB1MEN1KMT2ACA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0375355-B1 Process for the catalytic reforming of alkylene amines to linearly-extended polyalkylene polyamines DOW CHEMICAL CO (US) 1994-02-02 EP claimed
US-12091491-B2 Silylamine compound and latent curing agent comprising said silylamine compound KOEI CHEMICAL COMPANY, LIMITED (JP) 2024-09-17 US disclosed
US-20220119583-A1 SILYLAMINE COMPOUND AND LATENT CURING AGENT COMPRISING SAID SILYLAMINE COMPOUND KOEI CHEMICAL COMPANY, LIMITED (JP) 2022-04-21 US disclosed
EP-3875461-A1 SILYLAMINE COMPOUND AND LATENT CURING AGENT COMPRISING SAID SILYLAMINE COMPOUND Koei Chemical Company, Limited (JP) 2021-09-08 EP disclosed
CN-112930352-A Silylamine compound and latent curing agent containing the same 广荣化学株式会社 2021-06-08 CN disclosed
US-10190009-B2 Ink composition, ink jet recording method using same, and colored material NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2019-01-29 US disclosed
US-9587129-B2 Ink composition and ink set SEIKO EPSON CORPORATION (JP) 2017-03-07 US disclosed
US-20160160065-A1 INK COMPOSITION, INK JET RECORDING METHOD USING SAME, AND COLORED MATERIAL NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2016-06-09 US disclosed
US-20160137859-A1 INK COMPOSITION AND INK SET SEIKO EPSON CORPORATION (JP) 2016-05-19 US disclosed
EP-3015516-A1 INK COMPOSITION, INK JET RECORDING METHOD USING SAME, AND COLORED MATERIAL Nippon Kayaku Kabushiki Kaisha (JP) 2016-05-04 EP disclosed
US-5288909-A Group 5B catalyst, such as niobic acid THE DOW CHEMICAL COMPANY (US) 1994-02-22 US disclosed
WO-1994003835-A1 THERMALLY DEVELOPABLE PHOTOSENSITIVE MATERIAL POLAROID CORPORATION (US) 1994-02-17 WO disclosed
EP-0375355-B1 Process for the catalytic reforming of alkylene amines to linearly-extended polyalkylene polyamines DOW CHEMICAL CO (US) 1994-02-02 EP disclosed
US-5256786-A Catalytic reforming of cyclic alkyleneamines THE DOW CHEMICAL COMPANY (US) 1993-10-26 US disclosed
WO-1993018017-A1 CATALYTIC REFORMING OF CYCLIC ALKYLENEAMINES THE DOW CHEMICAL COMPANY (US) 1993-09-16 WO disclosed
US-5210307-A Thorium silicate catalyst THE DOW CHEMICAL COMPANY (US) 1993-05-11 US disclosed
US-5166442-A Group IIA metal silicates as catalysts THE DOW CHEMICAL COMPANY (US) 1992-11-24 US disclosed
US-5118850-A Catalytic reforming of alkyleneamines to linearly-extended polyalkylenepolyamines THE DOW CHEMICAL COMPANY (US) 1992-06-02 US disclosed
US-4996363-A Contacting with Group 2A metal silicate catalyst; aluminum-free THE DOW CHEMICAL COMPANY (US) 1991-02-26 US disclosed
EP-0375355-A2 Process for the catalytic reforming of alkylene amines to linearly-extended polyalkylene polyamines THE DOW CHEMICAL COMPANY (US) 1990-06-27 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 (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-20220119583-A1 SILYLAMINE COMPOUND AND LATENT CURING AGENT COMPRISING SAID SILYLAMINE COMPOUND CDKN1A, SIRT2, H1-4 ODC1 745/4885NFKB1 697/4885HTT 4234/4885
US-12091491-B2 Silylamine compound and latent curing agent comprising said silylamine compound CDKN1A, SIRT2, H1-4 ODC1 745/4885NFKB1 697/4885HTT 4234/4885

“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.