T-2000

T-2000

SCHEMBL711204

COCN1C(=O)N(COC)C(=O)C(c2ccccc2)(c2ccccc2)C1=O

nearest known ligand 0.69

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.69
CNR1 P21554 1/20 0.40
GPR55 Q9Y2T6 1/20 0.40
NPSR1 Q6W5P4 1/20 0.39
ELANE P08246 2/20 0.37
F2 P00734 1/20 0.37
PLG P00747 1/20 0.37
CTSG P08311 1/20 0.37
CMA1 P23946 1/20 0.37
CTRC Q99895 1/20 0.37
ALDH1A1 P00352 2/20 0.37
NPC1 O15118 1/20 0.36
BACE1 P56817 1/20 0.36
BACE2 Q9Y5Z0 1/20 0.36
POLB P06746 1/20 0.36
PLA2G7 Q13093 1/20 0.36
GAA P10253 1/20 0.35
CYP2C19 P33261 3/20 0.35
TSHR P16473 1/20 0.35
ATM Q13315 2/20 0.35

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
SCHEMBL14035379 0.91 LMNA (0.63) LMNACNR1GPR55NPSR1ALDH1A1
SCHEMBL13002842 0.89 LMNA (0.57) LMNACNR1GPR55NPSR1NPC1
SCHEMBL5873336 0.83 LMNA (0.54) LMNACNR1GPR55NPSR1ELANE
SCHEMBL711198 0.82 LMNA (0.52) LMNACNR1GPR55ALDH1A1NPC1
SCHEMBL1861854 0.81 LMNA (0.51) LMNACNR1GPR55ALDH1A1NPC1
SCHEMBL13002849 0.79 LMNA (0.46) LMNACNR1GPR55NPSR1ELANE
SCHEMBL3662305 0.77 LMNA (0.48) LMNACNR1GPR55ALDH1A1NPC1
SCHEMBL11278773 0.73 POLB (0.61) LMNACNR1NPC1POLBMEN1
SCHEMBL3662307 0.73 LMNA (0.43) LMNAELANEALDH1A1GAACYP2C19
SCHEMBL13241901 0.71 LMNA (0.51) LMNANPC1CYP2C19TSHRATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170348303-A1 PHARMACEUTICAL COMPOSITIONS CHARLESTON LABORATORIES, INC. 2017-12-07 US claimed
US-20140030322-A1 PHARMACEUTICAL COMPOSITIONS LOCL PHARMA, INC. 2014-01-30 US claimed
US-20120201888-A1 Pharmaceutical Compositions CHARLESTON LABORATORIES, INC. (US) 2012-08-09 US claimed
EP-2240022-A2 PHARMACEUTICAL COMPOSITIONS Charleston Laboratories, Inc. (US) 2010-10-20 EP claimed
WO-2009089494-A2 PHARMACEUTICAL COMPOSITIONS CHARLESTON LABORATORIES, INC. (US) 2009-07-16 WO claimed
US-20090175939-A1 PHARMACEUTICAL COMPOSITIONS CHARLESTON LABORATORIES, INC. (US) 2009-07-09 US claimed
EP-1311270-B1 NON-SEDATING BARBITURATE COMPOUNDS AS NEUROPROTECTIVE AGENTS TARO PHARMA IND (IL) 2008-01-09 EP claimed
US-20070167624-A1 Process for preparing 1-methoxymethyl 5,5-diphenybarbituric acid TARO PHARMACEUTICAL INDUSTRIES LTD. (US) 2007-07-19 US claimed
US-7227021-B2 Process for preparing 1-methoxymethyl-5,5-diphenylbarbituric acid TARA PHARMACEUTICAL INDUSTRIES LTD (IL) 2007-06-05 US claimed
EP-1781624-A2 A PROCESS FOR PREPARING 1-METHOXYMETHYL-5,5-DIPHENYLBARBITURIC ACID Taro Pharmaceutical Industries Ltd. (IL) 2007-05-09 EP claimed
US-20060004031-A1 Process for preparing 1-methoxymethyl-5,5-diphenylbarbituric acid TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2006-01-05 US claimed
US-20040224947-A1 Non-sedating barbiturate compounds as neuroprotective agents TARO PHARMACEUTICAL INDUSTRIES LTD (IL) 2004-11-11 US claimed
US-20040167358-A1 Method and reagents for N-alkylating ureides GUTMAN DANIELA (IL) 2004-08-26 US claimed
US-6756379-B2 USING SUCH AS 1,3-DIMETHOXYMETHYL-5,5-DIPHENYL-BARBITURIC ACID TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-06-29 US claimed
US-20030153589-A1 Non-sedating barbiturate compounds as neuroprotective agents TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2003-08-14 US claimed
EP-1311270-A1 NON-SEDATING BARBITURATE COMPOUNDS AS NEUROPROTECTIVE AGENTS TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2003-05-21 EP claimed
US-20030018080-A1 N-methoxymethyl-5,5-diphenylbarbituric acid TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2003-01-23 US claimed
WO-2002007729-A9 NON-SEDATING BARBITURATE COMPOUNDS AS NEUROPROTECTIVE AGENTS TARO PHARMA IND (IL) 2002-08-08 WO claimed
WO-2002007729-A1 NON-SEDATING BARBITURATE COMPOUNDS AS NEUROPROTECTIVE AGENTS TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2002-01-31 WO claimed
US-6093820-A REACTING AN IMIDE WITH A (SUBSTITUTED)ALKOXYALKYLSULFONIC ACID ESTER TO FORM A N-ALKOXYALKYL IMIDE SUCH AS METHOXYMETHYL ETHOSUXIMIDE; ADMINISTERING AS ANTICONVULSANT, ANTIANXIETY AGENT AND MUSCLE RELAXANT TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2000-07-25 US claimed

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-20030018080-A1 N-methoxymethyl-5,5-diphenylbarbituric acid MGMT, ALKBH3, ALKBH5 LMNA 2679/4885CNR1 801/4885GPR55 1056/4885
US-20040167358-A1 Method and reagents for N-alkylating ureides MGMT, ETV6, ALKBH3 LMNA 2608/4885CNR1 767/4885GPR55 1512/4885
US-20030153589-A1 Non-sedating barbiturate compounds as neuroprotective agents GABRB1, GABRB3, GABRB2 LMNA 2395/4885CNR1 268/4885GPR55 1625/4885
US-20040224947-A1 Non-sedating barbiturate compounds as neuroprotective agents GABRB1, GABRB2, GABRB3 LMNA 2733/4885CNR1 271/4885GPR55 1538/4885
US-20060004031-A1 Process for preparing 1-methoxymethyl-5,5-diphenylbarbituric acid ALKBH5, KDM5A, ALKBH1 LMNA 1095/4885CNR1 1424/4885GPR55 870/4885
US-20070167624-A1 Process for preparing 1-methoxymethyl 5,5-diphenybarbituric acid ALKBH5, KDM5A, ALKBH1 LMNA 1594/4885CNR1 1306/4885GPR55 393/4885

“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.