Aplindore

Aplindore

SCHEMBL119499

O=C1Cc2c(ccc3c2O[C@@H](CNCc2ccccc2)CO3)N1

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2

The experimentally established mechanism targets of Aplindore. 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
DRD2 known ✓ P14416 13/20 0.68
DRD4 P21917 7/20 0.68
DRD3 P35462 7/20 0.68
ALDH1A1 P00352 2/20 0.46
PARP1 P09874 1/20 0.45
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
SLC6A4 P31645 6/20 0.44
HTR2A P28223 2/20 0.44
HTR2B P41595 2/20 0.44
LMNA P02545 1/20 0.42

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
Aplindore SCHEMBL3192098 1.00 DRD2 (0.68) DRD2DRD4DRD3ALDH1A1PARP1
Aplindore SCHEMBL29359212 1.00 DRD2 (0.68) DRD2DRD4DRD3ALDH1A1PARP1
Aplindore SCHEMBL1231153 0.93 DRD2 (0.60) DRD2DRD4DRD3ALDH1A1PARP1
Aplindore SCHEMBL29470967 0.93 DRD2 (0.60) DRD2DRD4DRD3ALDH1A1PARP1
Aplindore SCHEMBL5954695 0.93 DRD2 (0.60) DRD2DRD4DRD3ALDH1A1PARP1
SCHEMBL5957109 0.91 DRD2 (0.58) DRD2DRD4DRD3ALDH1A1PARP1
SCHEMBL5957081 0.90 DRD2 (0.55) DRD2DRD4DRD3ALDH1A1MEN1
SCHEMBL5957139 0.90 DRD2 (0.55) DRD2DRD4DRD3ALDH1A1MEN1
Aplindore SCHEMBL3029385 0.88 DRD2 (0.54) DRD2DRD4DRD3ALDH1A1PARP1
SCHEMBL13481964 0.87 DRD2 (0.52) DRD2DRD4DRD3ALDH1A1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210060123-A1 THERAPEUTIC USE OF P75NTR NEUROTROPHIN BINDING PROTEIN LEVICEPT LTD (GB) 2021-03-04 US claimed
US-20180161392-A1 THERAPEUTIC USE OF P75NTR NEUROTROPHIN BINDING PROTEIN LEVICEPT LTD (GB) 2018-06-14 US claimed
EP-2825208-B1 P75NTR NEUROTROPHIN BINDING PROTEIN FOR THERAPEUTIC USE LEVICEPT LTD (GB) 2017-05-17 EP claimed
EP-2961730-A2 METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS XenoPort, Inc. (US) 2016-01-06 EP claimed
US-20150158809-A9 METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS XENOPORT, INC. (US) 2015-06-11 US claimed
US-20150037335-A1 THERAPEUTIC USE OF P75NTR NEUROTROPHIN BINDING PROTEIN LEVICEPT LTD (GB) 2015-02-05 US claimed
EP-2825208-A1 THERAPEUTIC USE OF P75NTR NEUROTROPHIN BINDING PROTEIN Levicept Ltd. (GB) 2015-01-21 EP claimed
EP-2175728-B1 SODIUM CHANNEL INHIBITORS ICAGEN INC (US) 2014-09-10 EP claimed
WO-2014134005-A2 METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS XENOPORT, INC. (US) 2014-09-04 WO claimed
US-20140243544-A1 METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS XENOPORT, INC. (US) 2014-08-28 US claimed
US-8062870-B2 Enantiomerically resolving acyloxyalkyl thiocarbonates used in synthesizing acyloxyalkyl carbamate prodrugs XENOPORT, INC. (US) 2011-11-22 US claimed
US-20090111837-A1 USE OF PDE7 INHIBITORS FOR THE TREATMENT OF NEUROPATHIC PAIN PFIZER INC. 2009-04-30 US claimed
CN-101146539-A Use of pde7 inhibitors for the treatment of neuropathic pain PFIZER LTD (GB) 2008-03-19 CN claimed
EP-1855686-A1 USE OF PDE7 INHIBITORS FOR THE TREATMENT OF NEUROPATHIC PAIN Pfizer Limited (GB) 2007-11-21 EP claimed
EP-1375503-B1 Dioxino derivatives and their use as dopanine agonists WYETH CORP (US) 2006-12-27 EP claimed
WO-2006092691-A1 USE OF PDE7 INHIBITORS FOR THE TREATMENT OF NEUROPATHIC PAIN PFIZER LIMITED (GB) 2006-09-08 WO claimed
US-20050095292-A1 Sustained release pharmaceutical compositions WYETH (US) 2005-05-05 US claimed
EP-1235570-A2 COMBINATIONS OF (S)-2-(BENZYLAMINO-METHYL)-2,3,8,9,-TETRAHYDRO-7H-1,4-DIOXINO(2,3)-E INDOL-8-ONE AND NEUROLEPTICS Wyeth (US) 2002-09-04 EP claimed
US-6350773-B1 Therapeutic combinations of (S)-2-(benzylamino-methyl)-2,3,8,9,-tetrahydro 7H-1,4-dioxino{2,3-e}indol-8-one and neuroleptics for the treatment or prevention of psychotic disorders AMERICAN HOME PRODUCTS CORPORATION 2002-02-26 US claimed
WO-2001041750-A2 COMBINATIONS OF (S)-2-(BENZYLAMINO-METHYL)-2,3,8,9,-TETRAHYDRO-7H-1,4-DIOXINO(2,3)-E INDOL-8-ONE AND NEUROLEPTICS WYETH (US) 2001-06-14 WO 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 (4 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-20050095292-A1 Sustained release pharmaceutical compositions ADCYAP1R1, ABCB11, SLC10A2 DRD2 3240/4885DRD4 3941/4885DRD3 3367/4885
US-20150158809-A9 METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS CPS1, CA7, NAAA DRD2 3241/4885DRD4 3217/4885DRD3 2698/4885
US-20140243544-A1 METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS CPS1, CA7, NAAA DRD2 3241/4885DRD4 3217/4885DRD3 2698/4885
US-20090111837-A1 USE OF PDE7 INHIBITORS FOR THE TREATMENT OF NEUROPATHIC PAIN PDE7A, PDE7B, PDE3A DRD2 3707/4885DRD4 3460/4885DRD3 3400/4885

“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.