SCHEMBL2886770

SCHEMBL2886770

C[C@H](N)C(=O)OC=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
SCHEMBL12211509 1.00
SCHEMBL272347 0.80 SLC7A5 (0.44)
SCHEMBL8924849 0.79
SCHEMBL1461506 0.78 SLC1A3 (0.32)
SCHEMBL524350 0.78
SCHEMBL3255288 0.78 TSHR (0.31)
SCHEMBL11292360 0.77
SCHEMBL7080309 0.77
SCHEMBL525402 0.77
Ammonia Solution, Strong SCHEMBL28494050 0.77 SLC1A3 (0.31)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2013167991-A1 COMPOSITIONS AND METHODS FOR THE TREATMENT OF METABOLIC DISORDERS KANDULA MAHESH (IN) 2013-11-14 WO disclosed
CN-102165333-A Method for producing optical sheet, optical sheet, and light source unit including optical sheet, display unit NIPPON CATALYTIC CHEM IND 2011-08-24 CN disclosed
CN-101889219-A Light diffuser and process for production of light diffuser NIPPON CATALYTIC CHEM IND 2010-11-17 CN disclosed
US-20100284170-A1 LIGHT DIFFUSER PLATE AND PROCESS FOR PRODUCTION OF LIGHT DIFFUSER PLATE NIPPON SHOKUBAI CO., LTD. (JP) 2010-11-11 US disclosed
EP-1773348-A4 TETRAPEPTIDE ANALOGS IDUN PHARMACEUTICALS INC (US) 2009-05-20 EP disclosed
EP-1773348-A2 TETRAPEPTIDE ANALOGS Idun Pharmaceuticals, Inc. (US) 2007-04-18 EP disclosed
WO-2006017295-A2 TETRAPEPTIDE ANALOGS IDUN PHARMACEUTICALS, INC. (US) 2006-02-16 WO disclosed
US-6011152-A REACTING STOICHIOMETRIC AMOUNTS OR MORE OF AN AMINO CARBOXYLIC ACID OR A PROTECTED/ACTIVATED FOR THEREOF WITH AN ACTIVATED DERVATIVE SELECTED FROM THE GROUP CONSISTING OF OXALATES AND MALONATES IN THE PRESENCE OF A SOLVENT AND HEAT CARNEGIE MELLON UNIVERSITY (US) 2000-01-04 US disclosed
US-4260683-A Process for producing antibacterial agents BRISTOL-MYERS COMPANY (US) 1981-04-07 US disclosed
US-4250170-A AMINOGLYCOSIDE ANTIBIOTIC BRISTOL-MYERS COMPANY (US) 1981-02-10 US disclosed