SCHEMBL1443821

SCHEMBL1443821

NC(=O)C(c1ccccc1)(c1ccc(F)cc1)c1ccccc1F

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ KCNN4 O15554 14/20 1.00
▸ KCNE1 P15382 1/20 1.00
▸ KCNQ1 P51787 1/20 1.00
▸ MLNR O43193 1/20 0.43
▸ NR1I2 O75469 1/20 0.43
▸ ADORA3 P0DMS8 1/20 0.43
▸ TBXA2R P21731 1/20 0.43
▸ CCKBR P32239 1/20 0.43
▸ OPRK1 P41145 1/20 0.43
▸ SLC6A3 Q01959 1/20 0.43
▸ KCNH2 Q12809 1/20 0.43
▸ NR1H4 Q96RI1 1/20 0.43
▸ KIF11 P52732 3/20 0.41
▸ MAPT P10636 1/20 0.41
▸ KMT2A Q03164 1/20 0.41
▸ NPC1 O15118 1/20 0.37
▸ RAB9A P51151 1/20 0.37

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
SCHEMBL12812130 1.00 KCNN4 (1.00) KCNN4KCNE1KCNQ1MLNRNR1I2
SCHEMBL12812145 1.00 KCNN4 (1.00) KCNN4KCNE1KCNQ1MLNRNR1I2
SCHEMBL1443968 0.97 KCNN4 (1.00) KCNN4KCNE1KCNQ1MLNRNR1I2
SCHEMBL2339426 0.93 KCNN4 (1.00) KCNN4KCNE1KCNQ1MLNRNR1I2
SCHEMBL1784375 0.93 KCNN4 (1.00) KCNN4KCNE1KCNQ1KIF11MAPT
SCHEMBL2332073 0.90 KCNN4 (1.00) KCNN4KCNE1KCNQ1KIF11MAPT
SCHEMBL12812582 0.88 KCNN4 (0.94) KCNN4KCNE1KCNQ1KIF11MAPT
SCHEMBL19872256 0.87 KCNN4 (0.76) KCNN4KCNE1KCNQ1MLNRNR1I2
SCHEMBL2337394 0.86 KCNN4 (1.00) KCNN4KCNE1KCNQ1KIF11MAPT
Senicapoc SCHEMBL1443805 0.86 KCNN4 (1.00) KCNN4KCNE1KCNQ1KIF11MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2003004010-A1 CARBONYLAMINO DERIVATIVES USEFUL FOR OBTAINING IMMUNE REGULATION POSEIDON PHARMACEUTICALS A/S (DK) 2003-01-16 — — WO claimed
US-10179115-B2 Methods for treating malaria using potassium channel inhibitors THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 2019-01-15 — — US disclosed
US-20180042872-A1 METHODS FOR TREATING MALARIA USING POTASSIUM CHANNEL INHIBITORS THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 2018-02-15 — — US disclosed
US-20180042872-A1 METHODS FOR TREATING MALARIA USING POTASSIUM CHANNEL INHIBITORS THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 2018-02-15 — — US disclosed
WO-2017070536-A1 METHODS AND AGENTS FOR TREATING DISEASES ANGION BIOMEDICA CORP. (US) 2017-04-27 — — WO disclosed
US-9428568-B2 Compositions and methods for modulating cell-cell fusion via intermediate-conductance calcium-activated potassium channels BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2016-08-30 — — US disclosed
US-20110300152-A1 COMPOSITIONS AND METHODS FOR MODULATING CELL-CELL FUSION VIA INTERMEDIATE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNELS YALE UNIVERSITY (US) 2011-12-08 — — US disclosed
CN-102272152-A Compositions and methods for modulating cell-cell fusion via intermediate-conductance calcium-activated potassium channels — 2011-12-07 — — CN disclosed
WO-2011034860-A1 TREATMENT METHODS USING TRIARYL METHANE COMPOUNDS ICAGEN, INC. (US) 2011-03-24 — — WO disclosed
US-20100056637-A1 TREATMENT METHODS USING TRIARYL METHANE COMPOUNDS ICAGEN, INC. (US) 2010-03-04 — — US disclosed
US-20070185209-A1 Treatment methods using triaryl methane compounds ICAGEN, INC. (US) 2007-08-09 — — US disclosed
US-20070185209-A1 Treatment methods using triaryl methane compounds ICAGEN, INC. (US) 2007-08-09 — — US disclosed
WO-2007075849-A2 TREATMENT METHODS USING TRIARYL METHANE COMPOUNDS ICAGEN, INC. (US) 2007-07-05 — — WO disclosed
CN-1193748-C Gardos channel antagonists ICAGEN INC (US) 2005-03-23 — — CN disclosed
EP-1158971-A4 GARDOS CHANNEL ANTAGONISTS ICAGEN INC (US) 2003-04-16 — — EP disclosed
WO-2003004010-A1 CARBONYLAMINO DERIVATIVES USEFUL FOR OBTAINING IMMUNE REGULATION POSEIDON PHARMACEUTICALS A/S (DK) 2003-01-16 — — WO disclosed
CN-1344158-A Gardos channel antagonists ICAGEN INC (US) 2002-04-10 — — CN disclosed
EP-1158971-A1 GARDOS CHANNEL ANTAGONISTS Icagen, Inc. (US) 2001-12-05 — — EP disclosed
US-6288122-B1 A TRIPHENYL ACETAMIDE ICAGEN, INC. 2001-09-11 — — US disclosed
WO-2000050026-A1 GARDOS CHANNEL ANTAGONISTS ICAGEN, INC. (US) 2000-08-31 — — 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 (5 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-20070185209-A1 Treatment methods using triaryl methane compounds KCNH3, KCNH2, KCNJ2 KCNN4 37/4885KCNE1 20/4885KCNQ1 23/4885
US-20110300152-A1 COMPOSITIONS AND METHODS FOR MODULATING CELL-CELL FUSION VIA INTERMEDIATE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNELS KCNN3, KCNN4, KCNMA1 KCNN4 2/4885KCNE1 68/4885KCNQ1 27/4885
US-20180042872-A1 METHODS FOR TREATING MALARIA USING POTASSIUM CHANNEL INHIBITORS KCNN1, KCNN2, KCNN3 KCNN4 10/4885KCNE1 41/4885KCNQ1 5/4885
US-10179115-B2 Methods for treating malaria using potassium channel inhibitors KCNN1, KCNN2, KCNN3 KCNN4 10/4885KCNE1 41/4885KCNQ1 5/4885
US-20100056637-A1 TREATMENT METHODS USING TRIARYL METHANE COMPOUNDS LTC4S, LTB4R2, CYSLTR2 KCNN4 2132/4885KCNE1 2203/4885KCNQ1 646/4885

“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.

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