SCHEMBL3806089

SCHEMBL3806089

CN1CCOCC1.CS(=O)(=O)O

nearest known ligand 0.50

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CA12 O43570 1/20 0.50
CA7 P43166 1/20 0.50
CA14 Q9ULX7 1/20 0.50
SMN1; SMN2 Q16637 5/20 0.43
TSHR P16473 4/20 0.43
L3MBTL1 Q9Y468 2/20 0.43
ALDH1A1 P00352 2/20 0.39
MAPK1 P28482 1/20 0.39
POLB P06746 1/20 0.38
CYP2C9 P11712 1/20 0.38
GAA P10253 1/20 0.38
HTT P42858 1/20 0.38

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
Sulfuric Acid SCHEMBL28051044 0.92 CA12 (0.52) CA12CA7CA14SMN1; SMN2TSHR
Sulfuric Acid SCHEMBL21616458 0.92 CA12 (0.52) CA12CA7CA14SMN1; SMN2TSHR
Sulfamate SCHEMBL27744770 0.88 CA7 (0.48) CA12CA7CA14SMN1; SMN2TSHR
SCHEMBL28051043 0.84 CA12 (0.44) CA12CA7CA14SMN1; SMN2TSHR
SCHEMBL3634165 0.84 CA12 (0.44) CA12CA7CA14SMN1; SMN2TSHR
Sulfuric Acid SCHEMBL2374802 0.82 CA12 (0.43) CA12CA7CA14SMN1; SMN2TSHR
Sulfuric Acid SCHEMBL7120564 0.82 CA12 (0.43) CA12CA7CA14SMN1; SMN2TSHR
Trifluoromethanesulfonic Acid SCHEMBL10942760 0.82 CA12 (0.43) CA12CA7CA14SMN1; SMN2TSHR
Methyl Alcohol SCHEMBL28612959 0.81
Hydrogen Peroxide SCHEMBL11793831 0.81

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120022522-A Drug-loaded microneedle, drug-loaded microneedle patch and electrically-controlled drug release microneedle system 成都邦迈医创科技有限公司 2025-05-23 CN claimed
CN-120022522-A Drug-loaded microneedle, drug-loaded microneedle patch and electrically-controlled drug release microneedle system 成都邦迈医创科技有限公司 2025-05-23 CN disclosed
CN-116848087-A Process for the preparation of aryl vinyl sulfones 凯米拉公司 2023-10-03 CN disclosed
CN-101812039-B Method for generating 5-hydroxymethylfurfural by using ionic liquid catalysis UNIV TIANJIN 2012-09-26 CN disclosed
US-20100292469-A1 PROCESS FOR THE PREPARATION OF N-TRIAZINYLAMMONIUM SALTS ITALVELLUTI S.P.A. (IT) 2010-11-18 US disclosed
CN-101812039-A Method for generating 5-hydroxymethylfurfural by using ionic liquid catalysis UNIV TIANJIN 2010-08-25 CN disclosed
CN-101671316-A Ion liquid based on morpholine cations and preparation method thereof DINGZHOU RADI GLORY BIOCHEMICA 2010-03-17 CN disclosed
EP-1794172-B1 ANTIVIRAL 4'-AZIDO-NUCLEOSIDES HOFFMANN LA ROCHE (CH) 2009-07-15 EP disclosed
EP-1951691-A1 PROCESS FOR THE PREPARATION OF N-TRIAZINYLAMMONIUM SALTS Italvelluti S.p.A. (IT) 2008-08-06 EP disclosed
US-7378402-B2 4-Amino-1-((2R,3S,4S,5R)-5-azido-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one; hepatitis C virus. ROCHE PALO ALTO LLC (US) 2008-05-27 US disclosed
EP-1794172-A1 ANTIVIRAL 4'-AZIDO-NUCLEOSIDES F.HOFFMANN-LA ROCHE AG (CH) 2007-06-13 EP disclosed
WO-2007051496-A1 PROCESS FOR THE PREPARATION OF N-TRIAZINYLAMMONIUM SALTS ITALVELLUTI S.P.A. (IT) 2007-05-10 WO disclosed
EP-1644395-B1 PROCESSES FOR PREPARING 4'AZIDO NUCLEOSIDE DERIVATIVES HOFFMANN LA ROCHE (CH) 2006-11-22 EP disclosed
CN-1809582-A Process for preparing 4' -azido nucleoside derivatives HOFFMANN LA ROCHE (CH) 2006-07-26 CN disclosed
EP-1644395-A1 PROCESSES FOR PREPARING 4'AZIDO NUCLEOSIDE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2006-04-12 EP disclosed
WO-2006021341-A1 ANTIVIRAL 4’-AZIDO-NUCLEOSIDES F. HOFFMANN-LA ROCHE AG (CH) 2006-03-02 WO disclosed
US-20060040890-A1 4-Amino-1-((2R,3S,4S,5R)-5-azido-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one; hepatitis C virus. ROCHE PALO ALTO LLC 2006-02-23 US disclosed
US-20050038240-A1 Processes for preparing 4'-azido-nucleoside derivatives ROCHE PALO ALTO LLC 2005-02-17 US disclosed
WO-2005000864-A1 PROCESSES FOR PREPARING 4’AZIDO NUCLEOSIDE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2005-01-06 WO 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-20050038240-A1 Processes for preparing 4'-azido-nucleoside derivatives NUDT1, RNGTT, DUT CA12 3095/4885CA7 1841/4885CA14 3532/4885
US-20060040890-A1 4-Amino-1-((2R,3S,4S,5R)-5-azido-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one; hepatitis C virus. HAVCR2, HCCS, CYP2S1 CA12 4861/4885CA7 4708/4885CA14 4722/4885

“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.