Sulfuric Acid

Sulfuric Acid

SCHEMBL6801606

O=S(=O)(O)O.c1ccc(-c2ccncc2)cc1

nearest known ligand 0.71

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
NOTUM Q6P988 1/20 0.71
MAPT P10636 3/20 0.52
LMNA P02545 1/20 0.52
NPC1 O15118 3/20 0.48
RAB9A P51151 3/20 0.48
ATAD2 Q6PL18 1/20 0.48
SMN1; SMN2 Q16637 5/20 0.47
POLB P06746 1/20 0.47
STAT3 P40763 1/20 0.47
KMT2A Q03164 2/20 0.46
MEN1 O00255 1/20 0.46
HSD17B10 Q99714 2/20 0.46
ALDH1A1 P00352 2/20 0.46
TP53 P04637 1/20 0.46
MAPK10 P53779 1/20 0.46
IKBKB O14920 1/20 0.45
CHUK O15111 1/20 0.45
IKBKE Q14164 1/20 0.45
PKMYT1 Q99640 1/20 0.45
NFKB1 P19838 1/20 0.44

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 SCHEMBL11418697 0.90 MAPT (0.65) NOTUMMAPTLMNANPC1RAB9A
SCHEMBL2331074 0.86 NOTUM (0.71) NOTUMMAPTLMNANPC1RAB9A
Biphenyl SCHEMBL1681197 0.84 ALDH1A1 (0.60) MAPTLMNASMN1; SMN2ALDH1A1MMP13
SCHEMBL124353 0.84 NOTUM (1.00) NOTUMMAPTLMNANPC1RAB9A
SCHEMBL1312790 0.84 NOTUM (1.00) NOTUMMAPTLMNANPC1RAB9A
Biphenyl SCHEMBL7077316 0.84 ALDH1A1 (0.60) MAPTLMNASMN1; SMN2ALDH1A1MMP13
SCHEMBL443953 0.82 NOTUM (0.94) NOTUMMAPTLMNANPC1RAB9A
Hydrochloric Acid SCHEMBL3862741 0.82 NOTUM (0.94) NOTUMMAPTLMNANPC1RAB9A
Bromide SCHEMBL10968966 0.82 NOTUM (0.94) NOTUMMAPTLMNANPC1RAB9A
Iodide SCHEMBL15720488 0.82 NOTUM (0.94) NOTUMMAPTLMNANPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6762303-B2 OXIDIZING A DIHYDROPYRIDINE COMPOUND IN THE PRESENCE OF NITROUS ACID OR A NITRITE OR A BASE AND HYDROGEN PEROXIDE SOLUTION FUJI PHOTO FILM CO., LTD. (JP) 2004-07-13 US disclosed
US-20020065420-A1 Method for producing pyridine compounds FUJIFILM CORPORATION (JP) 2002-05-30 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 (1 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-20020065420-A1 Method for producing pyridine compounds NOX1, NOX5, NOX4 NOTUM 1519/4885MAPT 3323/4885LMNA 2698/4885

“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.