Thiosulfuric Acid

Thiosulfuric Acid

SCHEMBL230065

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

nearest known ligand 0.50

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 11)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.50
KMT2A Q03164 2/20 0.50
ALDH1A1 P00352 1/20 0.50
TSHR P16473 1/20 0.50
CA4 P22748 3/20 0.35
FAHD1 Q6P587 1/20 0.35
CA1 P00915 1/20 0.33
CA5A P35218 1/20 0.31
CA5B Q9Y2D0 1/20 0.31
LDHA P00338 1/20 0.30
BLM P54132 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 SCHEMBL4209172 0.90 MEN1 (0.44) MEN1KMT2AALDH1A1TSHRCA4
Thiosulfuric Acid SCHEMBL145183 0.90 MEN1 (0.44) MEN1KMT2AALDH1A1TSHRCA4
Thiosulfuric Acid SCHEMBL1195014 0.90 ALDH1A1 (0.53) MEN1KMT2AALDH1A1TSHRCA1
Thiosulfuric Acid SCHEMBL230064 0.90 MEN1 (0.44) MEN1KMT2AALDH1A1TSHRCA4
Thiosulfuric Acid SCHEMBL29211051 0.87 MEN1 (0.50) MEN1KMT2AALDH1A1TSHRCA1
Sulfuric Acid SCHEMBL600964 0.86 TSHR (0.69) MEN1KMT2AALDH1A1TSHRCA4
Thiosulfuric Acid SCHEMBL262317 0.86
Thiosulfuric Acid SCHEMBL3422846 0.82 TSHR (0.61) MEN1KMT2AALDH1A1TSHRCA4
Thiosulfuric Acid SCHEMBL908689 0.82
Thiosulfuric Acid SCHEMBL10958542 0.82 TSHR (0.61) MEN1KMT2AALDH1A1TSHRCA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240158372-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF AMGEN INC. 2024-05-16 US disclosed
US-11780826-B2 Bisamide sarcomere activating compounds and uses thereof AMGEN INC. (US) 2023-10-10 US disclosed
CN-111601798-B Bisamide sarcomere activating compounds and uses thereof 美国安进公司 2023-08-11 CN disclosed
US-20220281850-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF AMGEN INC. 2022-09-08 US disclosed
EP-3494960-B1 STABILIZED COMPOSITIONS OF ALKYLATING AGENTS AND METHODS OF USING SAME HELSINN HEALTHCARE SA (CH) 2020-11-25 EP disclosed
CN-111601798-A Bisamide sarcomere activating compound and use thereof 美国安进公司 2020-08-28 CN disclosed
US-10723720-B2 Bisamide sarcomere activating compounds and uses therof AMGEN INC. (US) 2020-07-28 US disclosed
EP-3494960-A1 STABILIZED COMPOSITIONS OF ALKYLATING AGENTS AND METHODS OF USING SAME Helsinn Healthcare SA (CH) 2019-06-12 EP disclosed
US-20190077793-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF AMGEN INC. 2019-03-14 US disclosed
WO-2015130890-A9 SYNTHETIC SALT COMPLEXES FOR IMPROVEMENT OF PLANT GROWTH AND YIELD E. I. DU PONT DE NEMOURS AND COMPANY (US) 2016-09-29 WO disclosed
WO-2001057023-A1 HETEROCYCLIC AMIDE DERIVATIVES PFIZER PRODUCTS INC. (US) 2001-08-09 WO disclosed
EP-0654031-B1 STEREOSELECTIVE SYNTHESIS OF NUCLEOSIDE ANALOGUES USING BICYCLIC INTERMEDIATE IAF BIOCHEM INT (CA) 1999-12-29 EP disclosed
CN-1046720-C Stereoselective synthesis of nucleoside analogues using bicyclic intermediate IAF BIOCHEM INT (CA) 1999-11-24 CN disclosed
US-5763606-A Stereoselective synthesis of nucleoside analogues using bicyclic intermediate BIOCHEM PHARMA, INC. (CA) 1998-06-09 US disclosed
CN-1110479-A Stereoselective synthesis of nucleoside analogues using bicyclic intermediate IAF BIOCHEM INT (CA) 1995-10-18 CN disclosed
EP-0654031-A1 STEREOSELECTIVE SYNTHESIS OF NUCLEOSIDE ANALOGUES USING BICYCLIC INTERMEDIATE BIOCHEM PHARMA INC (CA) 1995-05-24 EP disclosed
WO-1994029301-A1 STEREOSELECTIVE SYNTHESIS OF NUCLEOSIDE ANALOGUES USING BICYCLIC INTERMEDIATE BIOCHEM PHARMA INC. (CA) 1994-12-22 WO disclosed
US-4233296-A STEROIDS HAVING PROGESTOMIMETIC PROPERTIES ROUSSEL UCLAF (FR) 1980-11-11 US disclosed
US-4147695-A 11β-Substituted-Δ9 -steroids ROUSSEL UCLAF (FR) 1979-04-03 US disclosed
US-3963772-A ACRYLIC TELOMERS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1976-06-15 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 (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-11780826-B2 Bisamide sarcomere activating compounds and uses thereof TNNI3, TNNT2, TNNC1 MEN1 4097/4885KMT2A 1593/4885ALDH1A1 3628/4885
US-20240158372-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF TNNI3, TNNT2, TNNC1 MEN1 4097/4885KMT2A 1593/4885ALDH1A1 3628/4885
US-20190077793-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF TNNI3, TNNT2, TNNC1 MEN1 4097/4885KMT2A 1593/4885ALDH1A1 3628/4885
US-10723720-B2 Bisamide sarcomere activating compounds and uses therof TNNI3, TNNT2, TNNC1 MEN1 3176/4885KMT2A 2746/4885ALDH1A1 4627/4885
US-20220281850-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF TNNI3, TNNT2, TNNC1 MEN1 4097/4885KMT2A 1593/4885ALDH1A1 3628/4885

“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.