Gacyclidine

Gacyclidine

SCHEMBL5402379

C[C@H]1CCCC[C@@]1(c1cccs1)N1CCCCC1.NC(=O)OCC(COC(N)=O)c1ccccc1

nearest known ligand 0.45

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3B

The experimentally established mechanism targets of Gacyclidine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.45
CYP2D6 P10635 2/20 0.45
PKM P14618 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
NPSR1 Q6W5P4 1/20 0.45
MEN1 O00255 2/20 0.40
PRCP P42785 2/20 0.40
KMT2A Q03164 2/20 0.40
SIGMAR1 Q99720 1/20 0.40
CHRM3 P20309 2/20 0.36
SLC6A9 P48067 2/20 0.35
OPRM1 P35372 2/20 0.34
OPRD1 P41143 1/20 0.34
OPRK1 P41145 1/20 0.34
OPRL1 P41146 1/20 0.34
GAA P10253 1/20 0.34
CYP3A4 P08684 2/20 0.33
CHRM2 P08172 1/20 0.33
HTR1A P08908 1/20 0.33
ADRA2A P08913 1/20 0.33

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
Gacyclidine SCHEMBL397836 0.79 SIGMAR1 (0.57) MEN1PRCPKMT2ASIGMAR1CHRM3
Gacyclidine SCHEMBL7190367 0.79 SIGMAR1 (0.57) MEN1PRCPKMT2ASIGMAR1CHRM3
Gacyclidine SCHEMBL4465879 0.79 SIGMAR1 (0.57) MEN1PRCPKMT2ASIGMAR1CHRM3
Gacyclidine SCHEMBL3457748 0.79 SIGMAR1 (0.57) MEN1PRCPKMT2ASIGMAR1CHRM3
Gacyclidine SCHEMBL5398234 0.78 SIGMAR1 (0.56) MEN1PRCPKMT2ASIGMAR1CHRM3
Gacyclidine SCHEMBL1662223 0.78 SIGMAR1 (0.56) MEN1PRCPKMT2ASIGMAR1CHRM3
SCHEMBL8206550 0.68 MEN1 (0.42) MEN1PRCPKMT2ASIGMAR1CHRM3
Felbamate SCHEMBL2946508 0.67 CYP1A2 (1.00) CYP1A2CYP2D6PKMSMN1; SMN2NPSR1
Felbamate SCHEMBL34947 0.67 CYP1A2 (1.00) CYP1A2CYP2D6PKMSMN1; SMN2NPSR1
Hydrochloric Acid SCHEMBL8205944 0.67 MEN1 (0.41) MEN1PRCPKMT2ASIGMAR1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2007518755-A 2007-07-12 JP claimed
EP-1708707-A1 PHARMACEUTICAL COMPOSITION COMPRISING A MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITOR AND AN N-METHYL-D-ASPARTATE (NMDA) RECEPTORS ANTAGONIST NEUROSEARCH A/S (DK) 2006-10-11 EP claimed
US-20050182089-A1 Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and an N-methyl-D-aspartate (NMDA) receptors antagonist BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2005-08-18 US claimed
WO-2005070429-A1 PHARMACEUTICAL COMPOSITION COMPRISING A MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITOR AND AN N-METHYL-D-ASPARTATE (NMDA) RECEPTORS ANTAGONIST NEUROSEARCH A/S (DK) 2005-08-04 WO claimed
EP-1708707-A1 PHARMACEUTICAL COMPOSITION COMPRISING A MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITOR AND AN N-METHYL-D-ASPARTATE (NMDA) RECEPTORS ANTAGONIST NEUROSEARCH A/S (DK) 2006-10-11 EP disclosed
US-20050182089-A1 Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and an N-methyl-D-aspartate (NMDA) receptors antagonist BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2005-08-18 US disclosed
WO-2005070429-A1 PHARMACEUTICAL COMPOSITION COMPRISING A MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITOR AND AN N-METHYL-D-ASPARTATE (NMDA) RECEPTORS ANTAGONIST NEUROSEARCH A/S (DK) 2005-08-04 WO 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 (1 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-20050182089-A1 Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and an N-methyl-D-aspartate (NMDA) receptors antagonist SLC18A2, SLC6A2, SLC6A3 CYP1A2 685/4885CYP2D6 341/4885PKM 800/4885

“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.