Tecalcet

Tecalcet

SCHEMBL311950

COc1cccc([C@@H](C)NCCCc2ccccc2Cl)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CASR

The experimentally established mechanism targets of Tecalcet. 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
CASR known ✓ P41180 13/20 1.00
HTR1A P08908 1/20 0.98
ADRA2B P18089 1/20 0.98
ADRA2C P18825 1/20 0.98
SLC6A2 P23975 1/20 0.98
HRH2 P25021 1/20 0.98
HTR2A P28223 1/20 0.98
HTR2C P28335 1/20 0.98
HRH1 P35367 1/20 0.98
OPRM1 P35372 1/20 0.98
DRD3 P35462 1/20 0.98
OPRK1 P41145 1/20 0.98
HTR2B P41595 1/20 0.98
HTR5A P47898 1/20 0.98
HTR6 P50406 1/20 0.98
TMEM97 Q5BJF2 1/20 0.98
GPR65 Q8IYL9 1/20 0.98
SIGMAR1 Q99720 1/20 0.98
SMN1; SMN2 Q16637 1/20 0.49
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
Tecalcet SCHEMBL1275509 1.00 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
Tecalcet SCHEMBL30092843 1.00 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
Tecalcet SCHEMBL31424074 1.00 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
Tecalcet SCHEMBL31424064 1.00 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
Tecalcet SCHEMBL896469 1.00 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
Tecalcet SCHEMBL29374613 0.99 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
Tecalcet SCHEMBL1178449 0.99 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
Tecalcet SCHEMBL1178446 0.99 CASR (1.00) CASRHTR1AADRA2BADRA2CSLC6A2
SCHEMBL6222202 0.96 CASR (0.93) CASRHTR1AADRA2BADRA2CSLC6A2
SCHEMBL7355756 0.92 CASR (0.84) CASRHTR1AADRA2BADRA2CSLC6A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260102414-A1 USE OF DERIVATIVES CONTAINING C-O-P BONDS IN PATIENTS WITH KIDNEY FAILURE SANIFIT THERAPEUTICS S A (ES) 2026-04-16 US claimed
US-20250295676-A1 INOSITOL PHOSPHATE COMPOUNDS FOR USE IN TREATING, INHIBITING THE PROGRESSION, OR PREVENTING CARDIOVASCULAR CALCIFICATION VIFOR (INTERNATIONAL) LTD. (CH) 2025-09-25 US claimed
US-20220249521-A1 USE OF DERIVATIVES CONTAINING C-O-P BONDS IN PATIENTS WITH KIDNEY FAILURE Sanifit Therapeutics S.A. (ES) 2022-08-11 US claimed
US-20190134054-A1 ASSOCIATION OF ANTAGONISTS OF THE VASOPRESSIN RECEPTOR AND CALCIMIMETICS, COMPOSITION AND USE THEREOF FOR THE TREATMENT OF POLYCYSTIC KIDNEY UNIVERSITA' DEGLI STUDI DI BARI ALDO MORO (IT) 2019-05-09 US claimed
EP-3427753-A1 COMBINATION OF ANTAGONISTS OF THE VASOPRESSIN RECEPTOR AND CALCIOMIMETICS, COMPOSITION AND USE THEREOF FOR THE TREATMENT OF POLYCYSTIC KIDNEY Università degli Studi di Bari "Aldo Moro" (IT) 2019-01-16 EP claimed
US-10010559-B2 Use of derivatives containing C-O-P bonds in patients with kidney failure LABORATORIOS SANIFIT, S.L. (ES) 2018-07-03 US claimed
US-20170020903-A1 USE OF DERIVATIVES CONTAINING C-O-P BONDS IN PATIENTS WITH KIDNEY FAILURE VIFOR (INTERNATIONAL) LTD. (CH) 2017-01-26 US 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-9016221-B2 Surface topographies for non-toxic bioadhesion control UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC. (US) 2015-04-28 US claimed
WO-2007061529-A1 LYOPHILIZATION PROCESS AND PRODUCTS OBTAINED THEREBY SCIDOSE LLC. (US) 2007-05-31 WO claimed
US-20070116729-A1 Lyophilization process and products obtained thereby SCIDOSE LLC 2007-05-24 US claimed
US-20070060625-A1 Methods of modulating intestinal fluid balance AMGEN INC. (US) 2007-03-15 US claimed
WO-2007027548-A2 METHODS OF MODULATING INTESTINAL FLUID BALANCE AMGEN INC. (US) 2007-03-08 WO claimed
US-20060276534-A1 Methods of decreasing calcification AMGEN INC. (US) 2006-12-07 US claimed
EP-1281702-A2 Calcium receptor active molecules NPS PHARMACEUTICALS, INC. (US) 2003-02-05 EP claimed
US-6313146-B1 CAN BE USED FOR THERAPY OF DISEASES OR DISORDERS IN A PATIENT BY MODULATING ONE OR MORE INORGANIC ION RECEPTOR ACTIVITIES NPS PHARMACEUTICALS, INC. 2001-11-06 US claimed
US-6031003-A TREATING A PATIENT HAVING A DISEASE OR DISORDER TREATABLE BY MODULATING ACTIVITY OF CALCIUM RECEPTORS IN VITRO BY ADMINISTERING A CALCIMIMETIC COMPOUND DETERMINED BY THE CALCILYTIC BOVINE PARATHYROID CELL TEST; OSTEOPOROSIS NPS PHARMACEUTICALS, INC. (US) 2000-02-29 US claimed
US-5504253-A Amine preparation NPS PHARMACEUTICALS, INC. (US) 1996-04-02 US claimed
WO-1996002492-A1 METHOD OF MAKING A BENZYLPROPANAMINE NSP PHARMACEUTICALS, INC. (US) 1996-02-01 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 (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-20170020903-A1 USE OF DERIVATIVES CONTAINING C-O-P BONDS IN PATIENTS WITH KIDNEY FAILURE ATP6V1B1, PROC, GC CASR 49/4885HTR1A 4771/4885ADRA2B 1630/4885
US-20250295676-A1 INOSITOL PHOSPHATE COMPOUNDS FOR USE IN TREATING, INHIBITING THE PROGRESSION, OR PREVENTING CARDIOVASCULAR CALCIFICATION PPIP5K2, INPP5B, IP6K3 CASR 46/4885HTR1A 4363/4885ADRA2B 3608/4885
US-20150158809-A9 METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS CPS1, CA7, NAAA CASR 1710/4885HTR1A 1381/4885ADRA2B 2797/4885
US-20220249521-A1 USE OF DERIVATIVES CONTAINING C-O-P BONDS IN PATIENTS WITH KIDNEY FAILURE ATP6V1B1, PROC, GC CASR 43/4885HTR1A 4777/4885ADRA2B 1684/4885
US-20060276534-A1 Methods of decreasing calcification CALCB, CALCA, CALCR CASR 9/4885HTR1A 4131/4885ADRA2B 1371/4885
US-20260102414-A1 USE OF DERIVATIVES CONTAINING C-O-P BONDS IN PATIENTS WITH KIDNEY FAILURE ATP6V1B1, IP6K3, IP6K1 CASR 28/4885HTR1A 4192/4885ADRA2B 1581/4885
US-10010559-B2 Use of derivatives containing C-O-P bonds in patients with kidney failure ATP6V1B1, PROC, GC CASR 43/4885HTR1A 4777/4885ADRA2B 1684/4885
US-20070060625-A1 Methods of modulating intestinal fluid balance SLC10A2, VIP, FABP2 CASR 23/4885HTR1A 2979/4885ADRA2B 1484/4885

“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.