SCHEMBL6567116

SCHEMBL6567116

CCNCP(=O)(O)O

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL21271950 0.82 MMP1 (0.40)
Iminobis(Methylphosphonic Acid) SCHEMBL357369 0.81 KDM4E (0.44)
SCHEMBL4422829 0.78
Diethylamine SCHEMBL29187214 0.78 TP53 (0.57)
Diethylamine SCHEMBL320756 0.78 TP53 (0.57)
Diethylamine SCHEMBL9484949 0.78 TP53 (0.57)
Diethylamine SCHEMBL1203507 0.78 TP53 (0.57)
Medronic Acid SCHEMBL10395759 0.77 MMP2 (0.59)
Hydrochloric Acid SCHEMBL16225606 0.76 ANPEP (0.52)
Diethylamine SCHEMBL29262325 0.75 TP53 (0.53)

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2001507695-A 2001-06-12 JP claimed
EP-0948507-A1 HYDROGENATION OF CYANOPHOSPHONATE DERIVATIVES MONSANTO COMPANY (US) 1999-10-13 EP claimed
US-5905163-A REDUCTION OF CYANO GROUP BY CATALYTIC HYDROGENATION MONSANTO COMPANY (US) 1999-05-18 US claimed
WO-1998029423-A1 HYDROGENATION OF CYANOPHOSPHONATE DERIVATIVES MONSANTO COMPANY (US) 1998-07-09 WO claimed
US-9150419-B2 Polycrystalline articles for reagent delivery US SYNTHETIC CORPORATION (US) 2015-10-06 US disclosed
US-8778874-B2 Glycopeptide antibiotic monomer derivatives NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2014-07-15 US disclosed
US-20040236144-A1 Method for producing $g(a)-aminophosphonic acids BASF AKTIENGESELLSCHAFT (DE) 2004-11-25 US disclosed
EP-1401847-A1 METHOD FOR PRODUCING $G(A)-AMINOPHOSPHONIC ACIDS BASF AKTIENGESELLSCHAFT (DE) 2004-03-31 EP disclosed
WO-2003000702-A1 METHOD FOR PRODUCING $G(A)-AMINOPHOSPHONIC ACIDS BASF AKTIENGESELLSCHAFT (DE) 2003-01-03 WO disclosed
US-5099056-A PROCESS FOR THE PRODUCTION OF N-SUBSTITUTED-AMINOMETHYLPHOSPHONIC ACID DIALKYLESTERS AND OF THE CORRESPONDING ACIDS KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 1992-03-24 US disclosed
EP-0385014-A1 Process for preparation of substituted aminomethylphosphonic acids CROMPTON &amp; KNOWLES CORPORATION (US) 1990-09-05 EP disclosed
EP-0385010-A1 N-alkyl-N-(Aminophenylsulfonyl)-aminoalkylphosphonic acids and salts CROMPTON &amp; KNOWLES CORPORATION (US) 1990-09-05 EP disclosed
US-4851158-A N-alkyl-N-(aminophenylsulfonyl)-aminoalkylphosphonic acids CROMPTON & KNOWLES CORPORATION (US) 1989-07-25 US disclosed
US-4830788-A Process for preparation of substituted-aminomethylphosphonic acids CROMPTON & KNOWLES CORPORATION (US) 1989-05-16 US disclosed
US-4804500-A Amine dealkylation process MONSANTO COMPANY (US) 1989-02-14 US disclosed
EP-0199702-B1 AMINE DEALKYLATION PROCESS Monsanto Company (US) 1988-12-21 EP disclosed
EP-0199702-A1 Amine dealkylation process Monsanto Company (US) 1986-10-29 EP disclosed
EP-0186648-A1 Process for the preparation of glyphosate and glyphosate derivatives Monsanto Company (US) 1986-07-02 EP disclosed