SCHEMBL6604556

SCHEMBL6604556

N[C@H]1C2CCN(CC2)[C@H]1C(c1ccccc1)c1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
TACR1 P25103 17/20 0.55
NPC1 O15118 1/20 0.49
MTOR P42345 1/20 0.49
RAB9A P51151 1/20 0.49

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
SCHEMBL9185372 1.00 TACR1 (0.55) TACR1NPC1MTORRAB9A
SCHEMBL8078188 1.00 TACR1 (0.55) TACR1NPC1MTORRAB9A
SCHEMBL13875665 1.00 TACR1 (0.55) TACR1NPC1MTORRAB9A
SCHEMBL472020 1.00 TACR1 (0.55) TACR1NPC1MTORRAB9A
SCHEMBL14364969 1.00 TACR1 (0.55) TACR1NPC1MTORRAB9A
SCHEMBL6135633 1.00 TACR1 (0.55) TACR1NPC1MTORRAB9A
SCHEMBL6135412 1.00 TACR1 (0.55) TACR1NPC1MTORRAB9A
SCHEMBL7121023 0.90 TACR1 (0.49) TACR1NPC1MTORRAB9A
SCHEMBL9537788 0.87 TACR1 (0.46) TACR1
SCHEMBL9532928 0.87 TACR1 (0.46) TACR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112557541-B Detection method of maropiptan citrate and related substances thereof 河北科技大学 2022-07-12 CN disclosed
CN-112557541-A Detection method of maropiptan citrate and related substances thereof 河北科技大学 2021-03-26 CN disclosed
EP-1713504-B1 ANTIMICROBIAL PRESERVATIVES TO ACHIEVE MULTI-DOSE FORMULATION USING BETA-CYCLODEXTRINS FOR LIQUID DOSAGE FORMS ZOETIS SERVICES LLC (US) 2017-06-07 EP disclosed
US-8183230-B2 Antimicrobial preservatives to achieve multi-dose formulation using beta-cyclodextrins for liquid dosage forms PFIZER INC. (US) 2012-05-22 US disclosed
US-20090099364-A1 Process for preparation of 1-(2s,3s)-2-benzhydryl-n-(5- tert-butyl-2-methoxybenzyl)quinuclidin-3-amine PFIZER INC. 2009-04-16 US disclosed
US-20090099364-A1 Process for preparation of 1-(2s,3s)-2-benzhydryl-n-(5- tert-butyl-2-methoxybenzyl)quinuclidin-3-amine PFIZER INC. 2009-04-16 US disclosed
EP-1713801-B1 PROCESS FOR PREPARATION OF 1-(2S,3S)-2-BENZHYDR YL-N-(5-TERT-BUTYL-2-METHOXYBENZYL)QUINUCLIDIN-3-AMINE PFIZER PROD INC (US) 2007-12-12 EP disclosed
US-20070155697-A1 Antimicrobial preservatives to achieve multi-dose formulation using beta-cyclodextrins for liquid dosage forms PFIZER INC. 2007-07-05 US disclosed
EP-1175417-B1 SUBSTITUTED BENZOLACTAM COMPOUNDS PFIZER PROD INC (US) 2004-01-07 EP disclosed
US-20030105124-A1 Substituted benzolactam compounds SOBOLOV-JAYNES SUSAN BETH (US) 2003-06-05 US disclosed
EP-0690835-A1 FORMYLATION PROCESS FOR AROMATIC ALDEHYDES PFIZER INC. (US) 1996-01-10 EP disclosed
EP-0668863-A1 QUINUCLIDINE DERIVATIVE AS SUBSTANCE P ANTAGONIST. PFIZER (US) 1995-08-30 EP disclosed
EP-0665844-A1 SUBSTITUTED BENZYLAMINOQUINUCLIDINES AS SUBSTANCE P ANTAGONISTS PFIZER INC. (US) 1995-08-09 EP disclosed
EP-0655996-A1 SUBSTITUTED BENZYLAMINO NITROGEN CONTAINING NON-AROMATIC HETEROCYCLES PFIZER INC. (US) 1995-06-07 EP disclosed
WO-1994004496-A9 SUBSTITUTED BENZYLAMINO NITROGEN CONTAINING NON-AROMATIC HETEROCYCLES 1995-01-26 WO disclosed
WO-1994024081-A1 FORMYLATION PROCESS FOR AROMATIC ALDEHYDES PFIZER INC. (US) 1994-10-27 WO disclosed
WO-1994011368-A1 QUINUCLIDINE DERIVATIVE AS SUBSTANCE P ANTAGONIST PFIZER INC. (US) 1994-05-26 WO disclosed
WO-1994008997-A1 SUBSTITUTED BENZYLAMINOQUINUCLIDINES AS SUBSTANCE P ANTAGONISTS PFIZER INC. (US) 1994-04-28 WO disclosed
US-5294744-A Formylation process for aromatic aldehydes PFIZER INC. (US) 1994-03-15 US disclosed
WO-1994004496-A1 SUBSTITUTED BENZYLAMINO NITROGEN CONTAINING NON-AROMATIC HETEROCYCLES PFIZER INC. (US) 1994-03-03 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 (3 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-20030105124-A1 Substituted benzolactam compounds NPY1R, HAX1, CBR1 TACR1 687/4885NPC1 1977/4885MTOR 3395/4885
US-20090099364-A1 Process for preparation of 1-(2s,3s)-2-benzhydryl-n-(5- tert-butyl-2-methoxybenzyl)quinuclidin-3-amine CS, GATD3, AQP1 TACR1 636/4885NPC1 1136/4885MTOR 2073/4885
US-20070155697-A1 Antimicrobial preservatives to achieve multi-dose formulation using beta-cyclodextrins for liquid dosage forms TBCD, CFTR, BTK TACR1 3742/4885NPC1 110/4885MTOR 117/4885

“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.