SCHEMBL5751334

SCHEMBL5751334

CS(=O)(=O)O.O=C1CCc2cc([C@H](O)CN3CCC(O)(c4cccc(F)c4)CC3)ccc2N1

nearest known ligand 0.90

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
GRIN2B known ✓ Q13224 4/20 0.49
HTR1A known ✓ P08908 1/20 0.41
DRD2 known ✓ P14416 1/20 0.41
HTR2A known ✓ P28223 1/20 0.41
KCNH2 Q12809 8/20 0.90
PKM P14618 1/20 0.42
ALDH1A1 P00352 1/20 0.40
OPRM1 P35372 1/20 0.40
OPRD1 P41143 1/20 0.40
OPRK1 P41145 1/20 0.40
OPRL1 P41146 1/20 0.40

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
SCHEMBL5753988 1.00 KCNH2 (0.90) KCNH2GRIN2BPKMHTR1ADRD2
SCHEMBL5751337 1.00 KCNH2 (0.90) KCNH2GRIN2BPKMHTR1ADRD2
SCHEMBL120402 0.95 KCNH2 (1.00) KCNH2GRIN2BHTR1ADRD2HTR2A
SCHEMBL2599445 0.95 KCNH2 (1.00) KCNH2GRIN2BHTR1ADRD2HTR2A
SCHEMBL877343 0.95 KCNH2 (1.00) KCNH2GRIN2BHTR1ADRD2HTR2A
SCHEMBL6769022 0.91 KCNH2 (0.73) KCNH2GRIN2BPKMHTR1ADRD2
SCHEMBL6769728 0.86 KCNH2 (0.80) KCNH2GRIN2BPKMHTR1ADRD2
SCHEMBL6765758 0.83 KCNH2 (0.76) KCNH2GRIN2BALDH1A1OPRM1OPRD1
Hydrochloric Acid SCHEMBL6765808 0.83 KCNH2 (0.75) KCNH2GRIN2BALDH1A1OPRM1OPRD1
SCHEMBL5457660 0.81 KCNH2 (0.59) KCNH2GRIN2BALDH1A1OPRM1OPRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1499606-B1 3, 4-DIHYDROQUINOLIN-2(1H)-ONE COMPOUNDS AS NR2B RECEPTOR ANTAGONISTS PFIZER (US) 2006-05-03 EP disclosed
US-6713490-B2 6-(2-(4-(3-FLUOROPHENYL)-4-HYDROXY-1-PIPERIDINYL)-1-HYDROXY -ETHYL)-3,4-DIHYDRO-2(1H)-QUINOLINONE; REDUCED INHIBITORY ACTIVITY AT HERG (HUMAN ETHER-A-GO-GO RELATED GENE) POTASSIUM CHANNEL PFIZER, INC. 2004-03-30 US disclosed
US-20030216430-A1 3, 4-dihydroquinolin-2(1H)-one compounds as NR2B receptor antagonists KAWAMURA MITSUHIRO (JP) 2003-11-20 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 (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-20030216430-A1 3, 4-dihydroquinolin-2(1H)-one compounds as NR2B receptor antagonists GRIN3B, GRIN1, GRIN2A GRIN2B 6/4885HTR1A 73/4885DRD2 174/4885

“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.