SCHEMBL9640608

SCHEMBL9640608

CCOC(=N)CC(=N)OCC

nearest known ligand 0.43

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MGAM O43451 1/20 0.43
GAA P10253 1/20 0.43
SI P14410 1/20 0.43
MGAM2 Q2M2H8 1/20 0.43
ALDH1A1 P00352 3/20 0.40
LMNA P02545 1/20 0.38
HSD17B10 Q99714 1/20 0.38
CA12 O43570 2/20 0.36
CA1 P00915 2/20 0.36
CA2 P00918 2/20 0.36
CA9 Q16790 2/20 0.36
ALOX15 P16050 1/20 0.36
SOAT1 P35610 1/20 0.36
TRPA1 O75762 1/20 0.33
EGLN1 Q9GZT9 1/20 0.31
DGAT1 O75907 1/20 0.30
MAPT P10636 1/20 0.30

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
Hydrochloric Acid SCHEMBL10722495 0.97 MGAM (0.41) MGAMGAASIMGAM2ALDH1A1
SCHEMBL4057076 0.81
SCHEMBL932146 0.81
SCHEMBL873457 0.81 GAA (0.67) MGAMGAASIMGAM2ALDH1A1
SCHEMBL9604212 0.80
Hydrochloric Acid SCHEMBL7367447 0.79 GAA (0.44) MGAMGAASIMGAM2ALDH1A1
Hydrochloric Acid SCHEMBL4057071 0.79 ALDH1A1 (0.46) MGAMGAASIMGAM2ALDH1A1
SCHEMBL8277426 0.79 GAA (0.50) MGAMGAASIMGAM2ALDH1A1
SCHEMBL9547351 0.79
Hydrochloric Acid SCHEMBL282717 0.79 GAA (0.64) MGAMGAASIMGAM2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250312347-A1 THERAPEUTIC BENEFIT OF SUBOPTIMALLY ADMINISTERED CHEMICAL COMPOUNDS BROWN DENNIS M (US) 2025-10-09 US disclosed
US-12336993-B2 Therapeutic benefit of suboptimally administered chemical compounds BROWN DENNIS M (US) 2025-06-24 US disclosed
US-20230133044-A1 THERAPEUTIC BENEFIT OF SUBOPTIMALLY ADMINISTERED CHEMICAL COMPOUNDS BROWN DENNIS M (US) 2023-05-04 US disclosed
US-11491154-B2 Therapeutic benefit of suboptimally administered chemical compounds BROWN DENNIS M (US) 2022-11-08 US disclosed
US-11446274-B2 Use of dianhydrogalactitol or derivatives or analogs thereof for treatment of pediatric central nervous system malignancies DEL MAR PHARMACEUTICALS (BC) LTD. (CA) 2022-09-20 US disclosed
WO-2021076681-A1 PROCESS FOR SYNTHESIS OF PICOLINAMIDES DOW AGROSCIENCES LLC (US) 2021-04-22 WO disclosed
EP-1931675-B1 PYRAZOLO(1, 5A) PYRIMIDINES AS PROTEIN KINASE INHIBITORS MERCK SHARP & DOHME (US) 2015-01-14 EP disclosed
US-8232393-B2 Aromatic AZA heterocycles, method of production and use of the material in organic electronics OSRAM OPTO SEMICONDUCTORS GMBH (DE) 2012-07-31 US disclosed
US-8232393-B2 Aromatic AZA heterocycles, method of production and use of the material in organic electronics OSRAM OPTO SEMICONDUCTORS GMBH (DE) 2012-07-31 US disclosed
US-8110679-B2 Nanofilm and membrane compositions COVALENT PARTNERS LLC (US) 2012-02-07 US disclosed
US-7595368-B2 Nanofilm compositions with polymeric components COVALENT PARTNERS, LLC (US) 2009-09-29 US disclosed
US-20090114596-A1 NANOFILM AND MEMBRANE COMPOSITIONS COVALENT PARTNERS LLC 2009-05-07 US disclosed
US-7432371-B2 Nanofilm and membrane compositions COVALENT PARTNERS, LLC (US) 2008-10-07 US disclosed
US-20070276145-A1 Method of Preparing a Ring Compound Having Two Adjacent Chiral Centers ICOS CORPORATION (US) 2007-11-29 US disclosed
US-20070276145-A1 Method of Preparing a Ring Compound Having Two Adjacent Chiral Centers ICOS CORPORATION (US) 2007-11-29 US disclosed
US-20070082902-A1 Pyrazolopyrimidines as protein kinase inhibitors SCHERING CORPORATION 2007-04-12 US disclosed
US-20070082902-A1 Pyrazolopyrimidines as protein kinase inhibitors SCHERING CORPORATION 2007-04-12 US disclosed
EP-0279366-B1 PROCESS FOR THE PREPARATION OF PYRIMIDINES HOECHST AKTIENGESELLSCHAFT (DE) 1992-08-12 EP disclosed
US-4960887-A REACTING PROPANEDIIMIDATE WITH CARBONIC ACID IMINEDERIVATIVE HOECHST AKTIENGESELLSCHAFT (DE) 1990-10-02 US disclosed
EP-0279366-A2 Process for the preparation of pyrimidines HOECHST AKTIENGESELLSCHAFT (DE) 1988-08-24 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 (7 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-20230133044-A1 THERAPEUTIC BENEFIT OF SUBOPTIMALLY ADMINISTERED CHEMICAL COMPOUNDS UNG, DPYD, TPMT MGAM 2375/4885GAA 999/4885SI 968/4885
US-20250312347-A1 THERAPEUTIC BENEFIT OF SUBOPTIMALLY ADMINISTERED CHEMICAL COMPOUNDS UNG, DPYD, TPMT MGAM 2375/4885GAA 999/4885SI 968/4885
US-11491154-B2 Therapeutic benefit of suboptimally administered chemical compounds UNG, DPYD, TPMT MGAM 2375/4885GAA 999/4885SI 968/4885
US-20070276145-A1 Method of Preparing a Ring Compound Having Two Adjacent Chiral Centers NISCH, NDC1, SUCLG2 MGAM 3029/4885GAA 1861/4885SI 456/4885
US-11446274-B2 Use of dianhydrogalactitol or derivatives or analogs thereof for treatment of pediatric central nervous system malignancies DCK, CDC7, DNMT1 MGAM 1475/4885GAA 2478/4885SI 1919/4885
US-12336993-B2 Therapeutic benefit of suboptimally administered chemical compounds UNG, DPYD, TPMT MGAM 2375/4885GAA 999/4885SI 968/4885
US-20070082902-A1 Pyrazolopyrimidines as protein kinase inhibitors CHEK1, CHEK2, BUB1 MGAM 4629/4885GAA 2665/4885SI 3610/4885

“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.