Thiosulfuric Acid

Thiosulfuric Acid

SCHEMBL1195014

O=C(O)O.O=S([O-])(O)=S.[Na+]

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GSK3AGSK3BIMPA1

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.53
MEN1 O00255 1/20 0.53
TSHR P16473 1/20 0.53
KMT2A Q03164 1/20 0.53
CA1 P00915 1/20 0.36
CA2 P00918 1/20 0.36
CA9 Q16790 1/20 0.36
CA5A P35218 1/20 0.33
CA5B Q9Y2D0 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.30

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
Thiosulfuric Acid SCHEMBL29211051 0.97 MEN1 (0.50) ALDH1A1MEN1TSHRKMT2ACA1
Thiosulfuric Acid SCHEMBL230065 0.90 MEN1 (0.50) ALDH1A1MEN1TSHRKMT2ACA1
Bicarbonate SCHEMBL31485808 0.89 MEN1 (0.47) ALDH1A1MEN1TSHRKMT2ACA1
Thiosulfuric Acid SCHEMBL1027061 0.89 MEN1 (0.47) ALDH1A1MEN1TSHRKMT2ACA1
Thiosulfuric Acid SCHEMBL262317 0.89
Thiosulfuric Acid SCHEMBL10770655 0.85
Thiosulfuric Acid SCHEMBL908689 0.85
Thiosulfuric Acid SCHEMBL29518665 0.85 TSHR (0.61) ALDH1A1MEN1TSHRKMT2ACA1
Thiosulfuric Acid SCHEMBL3422846 0.85 TSHR (0.61) ALDH1A1MEN1TSHRKMT2ACA1
Thiosulfuric Acid SCHEMBL10958542 0.85 TSHR (0.61) ALDH1A1MEN1TSHRKMT2ACA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7884128-B2 reacting 11-{[tert-butyl(dimethyl)silyl]oxy}-7-[(E)-2-formyl-1-methyleth-1-en-1-yl]-6,13a-dimethyl-2-phenyl-3a,6,7,10,11,12,13,13a-octahydro-9H-[1,3]dioxolo[4,5-f]oxacyclododecin-9-one with 2-methyl-3-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]propyl}oxiran-2-yl)pentane-3-ol, to form pladienolide analogues EISAI R&D MANAGEMENT CO., LTD. (JP) 2011-02-08 US disclosed
US-20100204490-A1 PROCESS FOR TOTAL SYNTHESIS OF PLADIENOLIDE B AND PLADIENOLIDE D KANADA REGINA MIKIE 2010-08-12 US disclosed
CN-101663296-A 12-membered ring macrolactam derivatives EISAI R&D MAN CO LTD 2010-03-03 CN disclosed
EP-1935893-A1 TOTAL SYNTHESIS OF PLADIENOLIDE B AND PLADIENOLIDE D Eisai R&D Management Co., Ltd. (JP) 2008-06-25 EP disclosed
US-20080021226-A1 Process for total synthesis of pladienolide B and pladienolide D EISAI R&D MANAGEMENT CO., LTD. 2008-01-24 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 (2 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-20100204490-A1 PROCESS FOR TOTAL SYNTHESIS OF PLADIENOLIDE B AND PLADIENOLIDE D CYP8B1, PLA2G2D, HPD ALDH1A1 2637/4885MEN1 3007/4885TSHR 2691/4885
US-20080021226-A1 Process for total synthesis of pladienolide B and pladienolide D TPD52L2, CYP8B1, HPD ALDH1A1 2011/4885MEN1 1894/4885TSHR 2611/4885

“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.