Sulfuric Acid

Sulfuric Acid

SCHEMBL3440665

Clc1nncc2ccccc12.O=S(=O)(O)O

nearest known ligand 0.45

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CALCRLCHRM1CHRM2CHRM3F2RMAOAMAOBMAP2K1MAP2K2NTRK1NTRK2NTRK3OPRD1OPRK1OPRM1P2RY12PKLRSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASLC18A2SLC6A2SLC6A3TLR7TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8dacAdacBdacCfolAftsImrcAmrcBmrdApolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmB1rpmB2rpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmHrpmIrpmJrpmJ2rpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsR1rpsR2rpsSrpsTrpsUrpsZykgMykgO

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
▸ MAOA known ✓ P21397 1/20 0.43
▸ ALDH1A1 P00352 5/20 0.43
▸ LMNA P02545 4/20 0.43
▸ KDM4E B2RXH2 3/20 0.43
▸ RAB9A P51151 3/20 0.43
▸ TP53 P04637 2/20 0.43
▸ CYP3A4 P08684 2/20 0.43
▸ GOT1 P17174 2/20 0.43
▸ SMN1; SMN2 Q16637 2/20 0.43
▸ MPO P05164 2/20 0.43
▸ CYP1A2 P05177 2/20 0.43
▸ CYP2D6 P10635 2/20 0.43
▸ NPC1 O15118 2/20 0.43
▸ PKM P14618 1/20 0.43
▸ PTGS1 P23219 1/20 0.43
▸ THPO P40225 1/20 0.43
▸ AOX1 Q06278 1/20 0.43
▸ ACOX1 Q15067 1/20 0.43
▸ EGFR P00533 7/20 0.42
▸ KDR P35968 7/20 0.42

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 SCHEMBL3440667 0.92 EGFR (0.43) ALDH1A1LMNAKDM4ERAB9ATP53
SCHEMBL147684 0.89 KDM4E (0.52) ALDH1A1LMNAKDM4ERAB9ATP53
SCHEMBL31146748 0.89 KDM4E (0.52) ALDH1A1LMNAKDM4ERAB9ATP53
Hydrochloric Acid SCHEMBL3440483 0.87 KDM4E (0.53) ALDH1A1LMNAKDM4ERAB9ATP53
SCHEMBL29178078 0.76 LMNA (0.44) ALDH1A1LMNAKDM4ERAB9ATP53
Hydralazine SCHEMBL8703662 0.75 ALDH1A1 (0.81) ALDH1A1LMNAKDM4ERAB9ATP53
SCHEMBL27679087 0.74 LMNA (0.38) ALDH1A1LMNAKDM4ERAB9ATP53
SCHEMBL10906806 0.72 GOT1 (0.48) ALDH1A1LMNAKDM4ERAB9AGOT1
SCHEMBL27740679 0.70 LMNA (0.46) ALDH1A1LMNAKDM4ERAB9ATP53
SCHEMBL27740684 0.69 LMNA (0.48) ALDH1A1LMNAKDM4ERAB9ATP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7807830-B2 Manufacture of pure hydralazine salts NAVINTA LLC (US) 2010-10-05 — — US disclosed
US-20090187018-A1 temperature-assisted dissolution of hydralazine. HCl in an aqueous solvent ( ethanol, methanol, tetrahydrofuran), treatment of the solution with a clarifying agent selected from chelating agents (EDTA), activated carbon, filtration to remove chelate compounds, cooling to precipitate hydralazine.HCl NAVINTA LLC (US) 2009-07-23 — — US disclosed
US-7531653-B2 Manufacture of pure hydralazine salts NAVINTA LLC (US) 2009-05-12 — — US disclosed
US-20070129546-A1 Manufacture of pure hydralazine salts NAVINTA LLC 2007-06-07 — — US disclosed
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