Dioxane

Dioxane

SCHEMBL3328111

C1COCCO1.O=C([O-])[O-].[H+].[H+]

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GSK3AGSK3BIMPA1

The experimentally established mechanism targets of Dioxane. 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
TTR P02766 1/20 0.46
SMN1; SMN2 Q16637 4/20 0.39
GAA P10253 1/20 0.39
CA1 P00915 3/20 0.39
CA12 O43570 2/20 0.39
CA9 Q16790 2/20 0.39
HSD17B10 Q99714 1/20 0.36
KDM4E B2RXH2 2/20 0.35
TSHR P16473 1/20 0.32
MEN1 O00255 2/20 0.32
KMT2A Q03164 2/20 0.32
TP53 P04637 1/20 0.32
ALDH1A1 P00352 1/20 0.31
CA4 P22748 1/20 0.31
FAHD1 Q6P587 1/20 0.31
USP2 O75604 1/20 0.31
PKM P14618 1/20 0.31
MMP1 P03956 1/20 0.31
MMP3 P08254 1/20 0.31
MMP8 P22894 1/20 0.31

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
Dioxane SCHEMBL1758720 0.92 TTR (0.46) TTRSMN1; SMN2GAACA1CA12
Dioxane SCHEMBL28141413 0.92 TTR (0.46) TTRSMN1; SMN2GAACA1CA12
Dioxane SCHEMBL1045521 0.92 TTR (0.46) TTRSMN1; SMN2GAACA1CA12
Dioxane SCHEMBL10803588 0.89 SMN1; SMN2 (0.43) TTRSMN1; SMN2GAACA1CA12
Bicarbonate SCHEMBL10990881 0.88 CA4 (0.43) TTRSMN1; SMN2GAACA1CA12
Bicarbonate SCHEMBL10990882 0.88
Bicarbonate SCHEMBL28325709 0.85 CA4 (0.40) TTRSMN1; SMN2GAACA1CA12
Dioxane SCHEMBL27496812 0.81 TTR (0.43) TTRSMN1; SMN2GAACA1CA12
Tetrahydrofuran SCHEMBL28850538 0.79 ALDH1A1 (0.53) TTRSMN1; SMN2GAACA1CA12
Tetrahydrofuran SCHEMBL11210402 0.79 ALDH1A1 (0.53) TTRSMN1; SMN2GAACA1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7737166-B2 Antifungal bicyclic hetero ring compounds DAIICHI SANKYO COMPANY, LIMITED (JP) 2010-06-15 US disclosed
US-20090143353-A1 such as 2-tert-Butyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile hydrochloride, a 1,6-beta-glucan synthetase inhibitor having potent growth inhibition, used treating a fungal infections; fungicides DAIICHI SANKYO COMPANY, LIMITED (JP) 2009-06-04 US disclosed
EP-1932837-A1 BICYCLO HETEROCYCLIC COMPOUND HAVING ANTIFUNGAL ACTION Daiichi Sankyo Company, Limited (JP) 2008-06-18 EP 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-20090143353-A1 such as 2-tert-Butyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile hydrochloride, a 1,6-beta-glucan synthetase inhibitor having potent growth inhibition, used treating a fungal infections; fungicides CTPS1, TPP1, STS TTR 2006/4885SMN1; SMN2 3267/4885GAA 62/4885

“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.