Telcagepant

Telcagepant

SCHEMBL1198535

O=C(N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(CC(F)(F)F)C1=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CALCRL

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

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
CALCRL known ✓ Q16602 20/20 1.00
RAMP1 O60894 1/20 1.00
CALCA P06881 1/20 1.00

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
Telcagepant SCHEMBL29371277 1.00 CALCRL (1.00) CALCRLRAMP1CALCA
Telcagepant SCHEMBL13345769 1.00 CALCRL (1.00) CALCRLRAMP1CALCA
Telcagepant SCHEMBL3176473 1.00 CALCRL (1.00) CALCRLRAMP1CALCA
Telcagepant SCHEMBL32659727 1.00 CALCRL (1.00) CALCRLRAMP1CALCA
Telcagepant SCHEMBL13025488 1.00 CALCRL (1.00) CALCRLRAMP1CALCA
Telcagepant SCHEMBL3678266 0.99 CALCRL (0.99) CALCRLRAMP1CALCA
Telcagepant SCHEMBL3678268 0.99 CALCRL (0.99) CALCRLRAMP1CALCA
Telcagepant SCHEMBL3678042 0.99 CALCRL (0.97) CALCRLRAMP1CALCA
Telcagepant SCHEMBL3678043 0.99 CALCRL (0.97) CALCRLRAMP1CALCA
Telcagepant SCHEMBL3682410 0.96 CALCRL (0.92) CALCRLRAMP1CALCA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3366286-A1 COMPOUNDS FOR TREATING SEPSIS Keller, Johannes (DE) 2018-08-29 EP claimed
US-7829699-B2 Process for the preparation of CGRP antagonist MERCK SHARP & DOHME CORP. (US) 2010-11-09 US claimed
US-20100009967-A1 SOLID DOSAGE FORMULATIONS OF TELCAGEPANT POTASSIUM MERCK SHARP & DOHME CORP. 2010-01-14 US claimed
WO-2010002763-A1 SOLID DOSAGE FORMULATIONS OF TELCAGEPANT POTASSIUM MERCK & CO., INC. (US) 2010-01-07 WO claimed
US-20090281306-A1 efficient synthesis for the preparation of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1 -carboxamide; salt formation of potassium salt forms; treating migraine and cluster headache MERCK SHARP & DOHME CORP. 2009-11-12 US claimed
EP-2007764-B1 PROCESS FOR THE PREPARATION OF CGRP ANTAGONIST MERCK & CO INC (US) 2009-08-26 EP claimed
US-20240066028-A1 COMPOSITIONS FOR IMPROVED DELIVERY OF CGRP INHIBITORS PFIZER IRELAND PHARMACEUTICALS (IE) 2024-02-29 US disclosed
US-20240066028-A1 COMPOSITIONS FOR IMPROVED DELIVERY OF CGRP INHIBITORS PFIZER IRELAND PHARMACEUTICALS (IE) 2024-02-29 US disclosed
US-11753408-B2 Compounds and method for blocking transmission of malarial parasite THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2023-09-12 US disclosed
WO-2022132989-A1 COMPOSITIONS FOR IMPROVED DELIVERY OF CGRP INHIBITORS BIOHAVEN PHARMACEUTICAL HOLDING COMPANY LTD. (US) 2022-06-23 WO disclosed
WO-2022109077-A1 COMPOSITIONS FOR IMPROVED DELIVERY OF CGRP INHIBITORS BIOHAVEN PHARMACEUTICAL HOLDING COMPANY LTD. (US) 2022-05-27 WO disclosed
US-20210246137-A1 COMPOUNDS AND METHOD FOR BLOCKING TRANSMISSION OF MALARIAL PARASITE THE UNITED STATES OF AMERICA,AS REPRESENTED BY THE SECRETARY,DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2021-08-12 US disclosed
WO-2020252368-A2 NEW THERAPEUTIC APPROACH TO LUNG DISEASE THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2020-12-17 WO disclosed
US-20070225272-A1 CGRP receptor antagonists MERCK SHARP & DOHME LLC 2007-09-27 US disclosed
US-7235545-B2 CGRP receptor antagonists MERCK & CO., INC. (US) 2007-06-26 US disclosed
US-7235545-B2 CGRP receptor antagonists MERCK & CO., INC. (US) 2007-06-26 US disclosed
US-7235545-B2 CGRP receptor antagonists MERCK & CO., INC. (US) 2007-06-26 US disclosed
US-20050256098-A1 CGRP receptor antagonists MERCK SHARP & DOHME LLC 2005-11-17 US disclosed
US-6953790-B2 CGRP receptor antagonists MERCK & CO., INC. (US) 2005-10-11 US disclosed
US-20040229861-A1 CGRP receptor antagonists MERCK SHARP & DOHME LLC 2004-11-18 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 (8 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-11753408-B2 Compounds and method for blocking transmission of malarial parasite PLK1, HSP90B1, CEP170 CALCRL 4345/4885RAMP1 4602/4885CALCA 4095/4885
US-20100009967-A1 SOLID DOSAGE FORMULATIONS OF TELCAGEPANT POTASSIUM KCNN1, KCNN2, KCNN3 CALCRL 1126/4885RAMP1 2254/4885CALCA 2077/4885
US-20240066028-A1 COMPOSITIONS FOR IMPROVED DELIVERY OF CGRP INHIBITORS CALCB, CALCA, CALCRL CALCRL 3/4885RAMP1 46/4885CALCA 2/4885
US-20040229861-A1 CGRP receptor antagonists CCKBR, CCKAR, CALCRL CALCRL 3/4885RAMP1 191/4885CALCA 21/4885
US-20050256098-A1 CGRP receptor antagonists CCKBR, BDKRB1, BDKRB2 CALCRL 6/4885RAMP1 187/4885CALCA 23/4885
US-20070225272-A1 CGRP receptor antagonists CCKBR, BDKRB1, BDKRB2 CALCRL 6/4885RAMP1 187/4885CALCA 23/4885
US-20090281306-A1 efficient synthesis for the preparation of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1 -carboxamide; salt formation of potassium salt forms; treating migraine and cluster headache KCNJ2, KCNN2, KCNN1 CALCRL 200/4885RAMP1 877/4885CALCA 181/4885
US-20210246137-A1 COMPOUNDS AND METHOD FOR BLOCKING TRANSMISSION OF MALARIAL PARASITE PLK1, HSP90B1, CEP170 CALCRL 4345/4885RAMP1 4602/4885CALCA 4095/4885

“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.