Monophosphothiamine

Monophosphothiamine

SCHEMBL94443

Cc1ncc(C[n+]2csc(CCOP(=O)(O)O)c2C)c(N)n1.[Cl-]

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ TDP1 Q9NUW8 1/20 0.98
▸ TKT P29401 9/20 0.84
▸ LMNA P02545 1/20 0.84
▸ HSP90AA1 P07900 1/20 0.68
▸ ALDH1A1 P00352 2/20 0.60
▸ KDM4E B2RXH2 1/20 0.57

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
Monophosphothiamine SCHEMBL29733068 1.00 TDP1 (0.98) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL3681710 0.99 TDP1 (0.96) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL642271 0.99 TDP1 (0.96) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL17768676 0.99 TDP1 (0.96) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL9159014 0.99 TDP1 (0.96) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL23151818 0.99 TDP1 (0.96) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL399485 0.99 TDP1 (0.96) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL29373566 0.99 TDP1 (1.00) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL94444 0.99 TDP1 (1.00) TDP1TKTLMNAHSP90AA1ALDH1A1
Monophosphothiamine SCHEMBL4302184 0.98 TDP1 (0.94) TDP1TKTLMNAHSP90AA1ALDH1A1

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 1182 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4747627-A1 METHODS AND SYSTEMS FOR PREDICTIVE CLASSIFICATION BY MASS SPECTROMETRY AND TRAINED LARGE SPECTRAL MODELS Matterworks Inc (US) 2026-05-27 — — EP claimed
US-20260097063-A1 ANTI-C5 ANTIBODY/C5 IRNA DOSING REGIMENS FOR TREATING C5-ASSOCIATED DISEASES REGENERON PHARMA (US) 2026-04-09 — — US claimed
EP-3889160-B1 THIAMINE COMPOUND, PREPARATION METHOD AND PHARMACEUTICAL COMPOSITION THEREOF SHANGHAI RAISING PHARMACEUTICAL CO LTD (CN) 2026-04-01 — — EP claimed
US-20260041634-A1 VISCOSITY REDUCING EXCIPIENTS AND COMBINATIONS THEREOF FOR HIGHLY CONCENTRATED NUCLEIC ACID COMPOSITIONS MERCK PATENT GMBH (DE) 2026-02-12 — — US claimed
US-20260022411-A1 MICROBIAL CELL FACTORIES PRODUCING THIAMINE BIOSYNTIA APS (DK) 2026-01-22 — — US claimed
US-20250332134-A1 COMPOSITIONS FOR USE NESTLE SA (CH) 2025-10-30 — — US claimed
EP-4608449-A1 ANTI-C5 ANTIBODY/C5 IRNA CO-FORMULATIONS AND COMBINATION THERAPIES Regeneron Pharmaceuticals, Inc. (US) 2025-09-03 — — EP claimed
US-20250228810-A1 COMPOSITIONS FOR USE NESTLE SA (CH) 2025-07-17 — — US claimed
US-20250228809-A1 COMPOSITIONS FOR USE NESTLE SA (CH) 2025-07-17 — — US claimed
WO-2025131987-A1 VISCOSITY REDUCING EXCIPIENTS AND COMBINATIONS THEREOF FOR LIQUID COMPOSITIONS COMPRISING A PROTEIN MERCK PATENT GMBH (DE) 2025-06-26 — — WO claimed
US-5681554-A CONTAINING DIVALENT CATION, HYDROLYZED PROTEIN AND A VITAMIN COSMAIR, INC. (US) 1997-10-28 — — US claimed
US-5679697-A Palladium complexes and methods for using same in the treatment of tumors GARNETT MCKEEN LABORATORY, INC. 1997-10-21 — — US claimed
EP-0730449-A1 NOVEL PALLADIUM COMPLEXES AND METHODS FOR USING SAME IN THE TREATMENT OF TUMORS AND PSORIASIS Garnett, Merrill (US) 1996-09-11 — — EP claimed
EP-0385379-B1 Extractive procedure of thiamine monophosphate from a solution of thiamine phosphates BASF AG (DE) 1995-06-21 — — EP claimed
WO-1995014466-A1 NOVEL PALLADIUM COMPLEXES AND METHODS FOR USING SAME IN THE TREATMENT OF TUMORS AND PSORIASIS GARNETT MERRILL (US) 1995-06-01 — — WO claimed
US-5047223-A Separation of phosphoric acid from aqueous solutions of thiamine phosphates BASF AKTIENGESELLSCHAFT (DE) 1991-09-10 — — US claimed
EP-0417953-A1 Process for producing thiamine phosphates KYOWA HAKKO KOGYO CO., LTD. (JP) 1991-03-20 — — EP claimed
US-4999112-A Using a Cation Exchanger Resin BASF AKTIENGESELLSCHAFT (DE) 1991-03-12 — — US claimed
EP-0385379-A1 Extractive procedure of thiamine monophosphate from a solution of thiamine phosphates BASF Aktiengesellschaft (DE) 1990-09-05 — — EP claimed
US-4717663-A XANTHOMONAS, CULTURES, AEROBIC, PANTOTHENIC ACID AND/OR THIAMINE (DERIVATIVE) THE NISSHIN OIL MILLS, LTD. (JP) 1988-01-05 — — US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-20260097063-A1 ANTI-C5 ANTIBODY/C5 IRNA DOSING REGIMENS FOR TREATING C5-ASSOCIATED DISEASES LDLR, CHRNG, FCGR2A TDP1 3420/4885TKT 4192/4885LMNA 316/4885
US-20260022411-A1 MICROBIAL CELL FACTORIES PRODUCING THIAMINE AHCY, SHMT1, MTHFD1 TDP1 1224/4885TKT 22/4885LMNA 4260/4885
US-20260041634-A1 VISCOSITY REDUCING EXCIPIENTS AND COMBINATIONS THEREOF FOR HIGHLY CONCENTRATED NUCLEIC ACID COMPOSITIONS TYMS, MTHFD1, TYMP TDP1 12/4885TKT 169/4885LMNA 935/4885

“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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