Sulfuric Acid

Sulfuric Acid

SCHEMBL1521031

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

nearest known ligand 0.49

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
CYP1A2 P05177 2/20 0.43
CASR P41180 1/20 0.43
TET2 Q6N021 3/20 0.40
KDM4A O75164 2/20 0.40
KDM4C Q9H3R0 2/20 0.40
KDM2A Q9Y2K7 2/20 0.40
TET3 O43151 1/20 0.40
FOLH1 Q04609 8/20 0.39
GABRP O00591 2/20 0.39
GABRD O14764 2/20 0.39
GABRA1 P14867 2/20 0.39
GABRB1 P18505 2/20 0.39
GABRG2 P18507 2/20 0.39
GABRB3 P28472 2/20 0.39
GABRA5 P31644 2/20 0.39
GABRA3 P34903 2/20 0.39
GABRA2 P47869 2/20 0.39
GABRB2 P47870 2/20 0.39
GABRA4 P48169 2/20 0.39
GABRE P78334 2/20 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
Sulfuric Acid SCHEMBL1521033 1.00 CYP1A2 (0.43) CYP1A2CASRTET2KDM4AKDM4C
SCHEMBL198528 0.92 CYP1A2 (0.50) CYP1A2TET2KDM4AKDM4CKDM2A
SCHEMBL198527 0.92 CYP1A2 (0.50) CYP1A2TET2KDM4AKDM4CKDM2A
Hydrochloric Acid SCHEMBL1934550 0.90 CYP1A2 (0.48) CYP1A2TET2KDM4AKDM4CKDM2A
Hydrochloric Acid SCHEMBL2257624 0.90 CYP1A2 (0.48) CYP1A2TET2KDM4AKDM4CKDM2A
SCHEMBL2984816 0.81 CYP1A2 (0.48) CYP1A2TET2KDM4AKDM4CKDM2A
SCHEMBL2984814 0.81 CYP1A2 (0.48) CYP1A2TET2KDM4AKDM4CKDM2A
SCHEMBL15405381 0.79 LMNA (0.42) CYP1A2FOLH1TSHRLMNAPMP22
Sulfuric Acid SCHEMBL1521198 0.79 TDP1 (0.37) CASRFOLH1MAPT
Sulfuric Acid SCHEMBL1521195 0.79 TDP1 (0.37) CASRFOLH1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102039179-B Catalytic composition for preparing amide and method for preparing amide CHINA PETROCHEMICAL DEV CORP 2013-03-06 CN claimed
US-8367865-B2 Method and catalyst composition for preparing amide China Petrichemical Development Corporation (TW) 2013-02-05 US claimed
CN-102039179-A Catalytic composition for preparing amide and method for preparing amide CHINA PETROCHEMICAL DEV CORP 2011-05-04 CN claimed
EP-2308831-A1 Method and catalyst composition comprising an amino acid-ionic liquid and a Bronsted acid, for preparing amide China Petrochemical Development Corporation (TW) 2011-04-13 EP claimed
US-20110077429-A1 METHOD AND CATALYST COMPOSITION FOR PREPARING AMIDE CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2011-03-31 US claimed
US-8552180-B2 Method for separating amide from amino acid ionic liquid CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2013-10-08 US disclosed
US-8524895-B2 Method for preparing amide CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2013-09-03 US disclosed
CN-102039179-B Catalytic composition for preparing amide and method for preparing amide CHINA PETROCHEMICAL DEV CORP 2013-03-06 CN disclosed
US-8367865-B2 Method and catalyst composition for preparing amide China Petrichemical Development Corporation (TW) 2013-02-05 US disclosed
US-20110105793-A1 METHOD FOR SEPARATING AMIDE FROM AMINO ACID IONIC LIQUID CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2011-05-05 US disclosed
CN-102039179-A Catalytic composition for preparing amide and method for preparing amide CHINA PETROCHEMICAL DEV CORP 2011-05-04 CN disclosed
EP-2308831-A1 Method and catalyst composition comprising an amino acid-ionic liquid and a Bronsted acid, for preparing amide China Petrochemical Development Corporation (TW) 2011-04-13 EP disclosed
US-20110077429-A1 METHOD AND CATALYST COMPOSITION FOR PREPARING AMIDE CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2011-03-31 US disclosed
US-20100063274-A1 METHOD FOR PREPARING AMIDE CHINA PETROCHEMICAL DEVELOPMENT CORPORATION, Taipei(Taiwan) (TW) 2010-03-11 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 (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-20110105793-A1 METHOD FOR SEPARATING AMIDE FROM AMINO ACID IONIC LIQUID ASNS, AADAT, SLC1A5 CYP1A2 4306/4885CASR 2571/4885TET2 4450/4885
US-20100063274-A1 METHOD FOR PREPARING AMIDE ASNS, KMO, AADAT CYP1A2 483/4885CASR 2954/4885TET2 1143/4885
US-20110077429-A1 METHOD AND CATALYST COMPOSITION FOR PREPARING AMIDE BCAT2, BCAT1, KYAT3 CYP1A2 858/4885CASR 4716/4885TET2 1517/4885

“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.