SCHEMBL16600116

SCHEMBL16600116

CCS(=O)(=O)N1CCN(c2ccc(COC3COC(Cn4ccnc4)(c4ccc(Cl)cc4Cl)OC3)cc2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
CYP17A1 P05093 20/20 1.00
CYP21A2 P08686 20/20 1.00
CYP11B1 P15538 19/20 1.00
CYP3A4 P08684 7/20 0.80
CYP19A1 P11511 7/20 0.80
CYP7A1 P22680 1/20 0.80

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
SCHEMBL16608216 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16600117 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16599723 0.94 CYP17A1 (0.89) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16599720 0.94 CYP17A1 (0.89) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16608555 0.94 CYP17A1 (0.89) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16599844 0.93 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16599848 0.93 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16608506 0.93 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16599852 0.92 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1
SCHEMBL16608386 0.92 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP19A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160244436-A1 NOVEL FUNCTIONALIZED 5-(PHENOXYMETHYL)-1,3-DIOXANE ANALOGS EXHIBITING CYTOCHROME P450 INHIBITION AND THEIR METHOD OF USE CORTENDO AB (PUBL) 2016-08-25 US claimed
EP-3049084-A1 NOVEL FUNCTIONALIZED 5-(PHENOXYMETHYL)-1,3-DIOXANE ANALOGS EXHIBITNG CYTOCHROME P450 INHIBITION Cortendo AB (publ) (US) 2016-08-03 EP claimed
WO-2015048311-A1 NOVEL FUNCTIONALIZED 5-(PHENOXYMETHYL)-1,3-DIOXANE ANALOGS EXHIBITNG CYTOCHROME P450 INHIBITION CORTENDO AB (PUBL) (US) 2015-04-02 WO claimed
US-20160244436-A1 NOVEL FUNCTIONALIZED 5-(PHENOXYMETHYL)-1,3-DIOXANE ANALOGS EXHIBITING CYTOCHROME P450 INHIBITION AND THEIR METHOD OF USE CORTENDO AB (PUBL) 2016-08-25 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-20160244436-A1 NOVEL FUNCTIONALIZED 5-(PHENOXYMETHYL)-1,3-DIOXANE ANALOGS EXHIBITING CYTOCHROME P450 INHIBITION AND THEIR METHOD OF USE CYP11B1, CYP11B2, CYP21A2 CYP17A1 4/4885CYP21A2 3/4885CYP11B1 1/4885

“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.