Eleclazine

Eleclazine

SCHEMBL16989319

O=C1c2cc(-c3ccc(OC(F)(F)F)cc3)ccc2OCCN1Cc1ncccn1.O=S(=O)(O)CCS(=O)(=O)O

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2

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

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ KCNH2 Q12809 5/20 0.88
▸ SCN1A P35498 1/20 0.88
▸ SCN4A P35499 1/20 0.88
▸ SCN5A Q14524 1/20 0.88
▸ SCN9A Q15858 1/20 0.88
▸ SCN2A Q99250 1/20 0.88
▸ SCN3A Q9NY46 1/20 0.88
▸ SCN8A Q9UQD0 1/20 0.88
▸ SCN10A Q9Y5Y9 1/20 0.88
▸ ROCK2 O75116 9/20 0.53
▸ ROCK1 Q13464 8/20 0.53
▸ TNIK Q9UKE5 5/20 0.41
▸ CYP2D6 P10635 4/20 0.40
▸ CYP2C9 P11712 4/20 0.40
▸ GPR142 Q7Z601 4/20 0.40
▸ CYP3A4 P08684 1/20 0.40
▸ HRH3 Q9Y5N1 1/20 0.39

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
Eleclazine SCHEMBL16989317 0.95 KCNH2 (0.88) KCNH2SCN1ASCN4ASCN5ASCN9A
Eleclazine SCHEMBL29377130 0.94 KCNH2 (1.00) KCNH2SCN1ASCN4ASCN5ASCN9A
Eleclazine SCHEMBL14480722 0.94 KCNH2 (1.00) KCNH2SCN1ASCN4ASCN5ASCN9A
Eleclazine SCHEMBL16989336 0.93 KCNH2 (0.98) KCNH2SCN1ASCN4ASCN5ASCN9A
Eleclazine SCHEMBL16989316 0.93 KCNH2 (0.84) KCNH2SCN1ASCN4ASCN5ASCN9A
Eleclazine SCHEMBL16989318 0.91 KCNH2 (0.91) KCNH2SCN1ASCN4ASCN5ASCN9A
Eleclazine SCHEMBL16989341 0.90 KCNH2 (0.80) KCNH2SCN1ASCN4ASCN5ASCN9A
Eleclazine SCHEMBL19923836 0.87 KCNH2 (0.84) KCNH2SCN1ASCN4ASCN5ASCN9A
SCHEMBL17014542 0.87 SCN1A (0.86) KCNH2SCN1ASCN4ASCN5ASCN9A
SCHEMBL14480581 0.86 SCN1A (0.85) KCNH2SCN1ASCN4ASCN5ASCN9A

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9273038-B2 Solid forms of an ion channel modulator GILEAD SCIENCES, INC. (US) 2016-03-01 — — US claimed
US-20150225383-A1 SOLID FORMS OF AN ION CHANNEL MODULATOR GILEAD SCIENCES, INC. 2015-08-13 — — US claimed
EP-3105227-A1 SOLID FORMS OF AN ION CHANNEL MODULATOR Gilead Sciences, Inc. (US) 2016-12-21 — — EP disclosed
US-9273038-B2 Solid forms of an ion channel modulator GILEAD SCIENCES, INC. (US) 2016-03-01 — — US disclosed
WO-2015123434-A1 SOLID FORMS OF AN ION CHANNEL MODULATOR GILEAD SCIENCES, INC. (US) 2015-08-20 — — WO disclosed
US-20150225383-A1 SOLID FORMS OF AN ION CHANNEL MODULATOR GILEAD SCIENCES, INC. 2015-08-13 — — 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 (1 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-20150225383-A1 SOLID FORMS OF AN ION CHANNEL MODULATOR KCNN1, SCN4A, KCNN2 KCNH2 13/4885SCN1A 19/4885SCN4A 2/4885

“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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