Sulfuric Acid

Sulfuric Acid

SCHEMBL1626445

O=C(O)CN(c1ccccc1)c1ccccc1.O=S(=O)(O)O

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Sulfuric Acid. 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
SCN9A known ✓ Q15858 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.42
KEAP1 Q14145 1/20 0.42
NFE2L2 Q16236 1/20 0.42
MTNR1A P48039 1/20 0.42
MTNR1B P49286 1/20 0.42
NPSR1 Q6W5P4 2/20 0.41
CACNA2D1 P54289 1/20 0.41
CACNA1B Q00975 1/20 0.41
CACNB1 Q02641 1/20 0.41
HSP90AA1 P07900 1/20 0.40
ALDH1A1 P00352 3/20 0.39
TSHR P16473 2/20 0.39
NPC1 O15118 1/20 0.39
POLB P06746 1/20 0.39
HTT P42858 1/20 0.39
RAB9A P51151 1/20 0.39
KMT2A Q03164 1/20 0.39
GLA P06280 1/20 0.39

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
SCHEMBL440156 0.91 NPSR1 (0.48) L3MBTL1SMN1; SMN2MTNR1AMTNR1BNPSR1
Water SCHEMBL28256553 0.89 NPSR1 (0.46) L3MBTL1SMN1; SMN2MTNR1AMTNR1BNPSR1
Sulfuric Acid SCHEMBL9324944 0.82 HSP90AA1 (0.43) L3MBTL1SMN1; SMN2KEAP1NFE2L2NPSR1
SCHEMBL28088208 0.82 SCN9A (0.44) L3MBTL1SMN1; SMN2MTNR1AMTNR1BNPSR1
SCHEMBL9632432 0.80 KEAP1 (0.51) SMN1; SMN2KEAP1NFE2L2MTNR1AMTNR1B
SCHEMBL5690847 0.80 ALDH1A1 (0.52) L3MBTL1SMN1; SMN2MTNR1AMTNR1BNPSR1
SCHEMBL11341409 0.80 KEAP1 (0.45) L3MBTL1SMN1; SMN2KEAP1NFE2L2MTNR1A
Toluene SCHEMBL9461781 0.80 KEAP1 (0.44) KEAP1NFE2L2MTNR1AMTNR1BNPSR1
SCHEMBL2484595 0.80 CACNA2D1 (0.49) L3MBTL1SMN1; SMN2KEAP1NFE2L2NPSR1
SCHEMBL2485185 0.80 SCN9A (0.52) KEAP1NFE2L2MTNR1AMTNR1BTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7927843-B2 Method of preparing 2-deoxyribose 5-phosphate YUKI GOSEI KOGYO CO., LTD. (JP) 2011-04-19 US disclosed
US-7927842-B2 Method of preparing 2-deoxyribose 5-phosphate YUKI GOSEI KOGYO CO. LTD. (JP) 2011-04-19 US disclosed
EP-1364041-B1 METHOD OF PREPARING 2-DEOXYRIBOSE 5-PHOSPHATE YUKI GOSEI YAKUHIN KOGYO KK (JP) 2009-10-28 EP disclosed
US-20070298468-A1 Method of preparing 2-deoxyribose 5-phosphate SHIMIZU SAKAYU 2007-12-27 US disclosed
US-20070298467-A1 Method of preparing 2-deoxyribose 5-phosphate SHIMIZU SAKAYU 2007-12-27 US disclosed
US-7270992-B2 Method of preparing 2-deoxyribose 5-phosphate NOVARTIS AG (CH) 2007-09-18 US disclosed
CN-1494596-A Method of preparing 2-deoxyribose 5-phosphate 有机合成药品工业株式会社 2004-05-05 CN disclosed
US-20040038351-A1 Method of preparing 2-deoxyribose 5-phosphate NOVARTIS AG (CH) 2004-02-26 US disclosed
EP-1364041-A2 METHOD OF PREPARING 2-DEOXYRIBOSE 5-PHOSPHATE YUKI GOSEI KOGYO CO., LTD. (JP) 2003-11-26 EP disclosed
WO-2002070724-A2 METHOD OF PREPARING 2-DEOXYRIBOSE 5-PHOSPHATE YUKI GOSEI KOGYO CO., LTD. (JP) 2002-09-12 WO disclosed