SCHEMBL3881699

SCHEMBL3881699

C[C@H](NCCN[C@@H](C)c1ccccc1)c1ccccc1

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 3/20 0.76
LMNA P02545 2/20 0.76
CHRM2 P08172 1/20 0.76
HTR1A P08908 1/20 0.76
ADRA2A P08913 1/20 0.76
ADORA3 P0DMS8 1/20 0.76
CHRM1 P11229 1/20 0.76
SMPD1 P17405 1/20 0.76
DRD1 P21728 1/20 0.76
TBXA2R P21731 1/20 0.76
SLC6A2 P23975 1/20 0.76
SLC6A4 P31645 1/20 0.76
ADRA1A P35348 1/20 0.76
OPRM1 P35372 1/20 0.76
DRD3 P35462 1/20 0.76
CASR P41180 1/20 0.76
HTR2B P41595 1/20 0.76
SLC6A3 Q01959 1/20 0.76
KCNH2 Q12809 1/20 0.76
CYP1A2 P05177 1/20 0.76

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
SCHEMBL24406703 1.00 CYP3A4 (0.76) CYP3A4LMNACHRM2HTR1AADRA2A
SCHEMBL3881700 1.00 CYP3A4 (0.76) CYP3A4LMNACHRM2HTR1AADRA2A
SCHEMBL5471668 1.00 CYP3A4 (0.76) CYP3A4LMNACHRM2HTR1AADRA2A
Hydrochloric Acid SCHEMBL9633453 0.98 KMT2A (0.77) CYP3A4LMNACHRM2HTR1AADRA2A
Hydrochloric Acid SCHEMBL9633690 0.98 KMT2A (0.77) CYP3A4LMNACHRM2HTR1AADRA2A
SCHEMBL11094399 0.91 MTOR (0.75) CYP3A4LMNACHRM2HTR1AADRA2A
SCHEMBL1101513 0.91 CYP3A4 (0.70) CYP3A4LMNACHRM2HTR1AADRA2A
SCHEMBL5461331 0.91 CYP3A4 (0.70) CYP3A4LMNACHRM2HTR1AADRA2A
SCHEMBL10779809 0.91 CYP3A4 (0.70) CYP3A4LMNACHRM2HTR1AADRA2A
SCHEMBL12964248 0.89 CYP3A4 (0.68) CYP3A4LMNACHRM2HTR1AADRA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0577171-A2 Use of piperazine acetamide derivatives against reperfusion damage JANSSEN PHARMACEUTICA N.V. (BE) 1994-01-05 EP claimed
US-20190031695-A1 Methods and Compositions for Substituted Alpha-Aminophosphonate Analogues THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION ON BEHALF OF THE UNIV OF (US) 2019-01-31 US disclosed
US-20170267707-A1 Methods and Compositions for Substituted Alpha-Aminophosphonate Analogues THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION ON BEHALF OF THE UNIVERSITY OF NEVADA, LAS VEGAS 2017-09-21 US disclosed
US-20170267707-A1 Methods and Compositions for Substituted Alpha-Aminophosphonate Analogues THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION ON BEHALF OF THE UNIVERSITY OF NEVADA, LAS VEGAS 2017-09-21 US disclosed
EP-1483273-B1 LIGANDS FOR ASYMMETRIC REACTIONS SOLVIAS AG (CH) 2009-01-07 EP disclosed
US-7407910-B2 Ligands for asymmetric reactions SOLVIAS AG (CH) 2008-08-05 US disclosed
US-20060241307-A1 Bidentate having a heterocyclic ring, especially benzothiophene, 2,3-disubstituted with phosphonate, phosphine, phosphine oxide, dioxyphosphine or diaminophosphine groups; transition metal complexes; hydrogenation, isomerizatioin, hydroformylation, hydroboration, hydrosilylation or hydrocyanation BERENS ULRICH 2006-10-26 US disclosed
US-7094907-B2 Ligands for asymmetric reactions SOLVIAS AG (CH) 2006-08-22 US disclosed
US-20040260091-A1 Ligands for asymmetric reactions SOLVIAS AG (CH) 2004-12-23 US disclosed
EP-1483273-A2 LIGANDS FOR ASYMMETRIC REACTIONS Solvias AG (CH) 2004-12-08 EP disclosed
US-6573395-B2 Zinc complex with a chiral ligand, such as diethylzinc((S,S)-N-N'-ethylene-bis-(1-phenylethylamine)) FIRMENICH SA (CH) 2003-06-03 US disclosed
WO-2003031456-A2 LIGANDS FOR ASYMMETRIC REACTIONS SOLVIAS AG (CH) 2003-04-17 WO disclosed
EP-1012131-B1 ENANTIOSELECTIVE REDUCTION OF KETONES WITH A SILANE AGENT/METAL COMPOUND/CHIRAL LIGAND SYSTEM FIRMENICH & CIE (CH) 2003-03-19 EP disclosed
US-20020161252-A1 Zinc complex with a chiral ligand, such as diethylzinc((S,S)-N-N'-ethylene-bis-(1-phenylethylamine)) FIRMENICH SA, A SWISS COMPANY 2002-10-31 US disclosed
US-6392103-B1 USING ORGANOMETALLIC COMPOUND AS CATALYST FIRMENICH SA (CH) 2002-05-21 US disclosed
EP-1012131-A1 ENANTIOSELECTIVE REDUCTION OF KETONES WITH A SILANE AGENT/METAL COMPOUND/CHIRAL LIGAND SYSTEM FIRMENICH SA (CH) 2000-06-28 EP disclosed
WO-1999012877-A1 ENANTIOSELECTIVE REDUCTION OF KETONES WITH A SILANE AGENT/METAL COMPOUND/CHIRAL LIGAND SYSTEM FIRMENICH S.A. (CH) 1999-03-18 WO disclosed
WO-1991007967-A2 METHOD OF PREVENTING OR LIMITING REPERFUSION DAMAGE JANSSEN PHARMACEUTICA N.V. (BE) 1991-06-13 WO disclosed
US-4204997-A Asymmetric amination of 1,3-dienes MONSANTO COMPANY (US) 1980-05-27 US 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 (5 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-20170267707-A1 Methods and Compositions for Substituted Alpha-Aminophosphonate Analogues NPEPPS, AGPS, PHOSPHO1 CYP3A4 3167/4885LMNA 2248/4885CHRM2 3936/4885
US-20020161252-A1 Zinc complex with a chiral ligand, such as diethylzinc((S,S)-N-N'-ethylene-bis-(1-phenylethylamine)) ERH, POLH, PNMT CYP3A4 1202/4885LMNA 1045/4885CHRM2 1849/4885
US-20060241307-A1 Bidentate having a heterocyclic ring, especially benzothiophene, 2,3-disubstituted with phosphonate, phosphine, phosphine oxide, dioxyphosphine or diaminophosphine groups; transition metal complexes; hydrogenation, isomerizatioin, hydroformylation, hydroboration, hydrosilylation or hydrocyanation NR2E3, WNK2, OXSR1 CYP3A4 1948/4885LMNA 3394/4885CHRM2 20/4885
US-20040260091-A1 Ligands for asymmetric reactions COASY, ICMT, AP2M1 CYP3A4 72/4885LMNA 4664/4885CHRM2 1607/4885
US-20190031695-A1 Methods and Compositions for Substituted Alpha-Aminophosphonate Analogues NPEPPS, AGPS, PHOSPHO1 CYP3A4 3167/4885LMNA 2248/4885CHRM2 3936/4885

“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.