Sulfuric Acid

Sulfuric Acid

SCHEMBL7488838

O=S(=O)([O-])[O-].[Cu+2].c1cnc2c(c1)ccc1ncccc12.c1cnc2c(c1)ccc1ncccc12

nearest known ligand 0.77

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Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

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
▸ LMNA P02545 3/20 0.77
▸ CYP3A4 P08684 2/20 0.53
▸ KDM4E B2RXH2 6/20 0.48
▸ MAPT P10636 5/20 0.48
▸ HTT P42858 3/20 0.48
▸ TDP1 Q9NUW8 3/20 0.48
▸ SMN1; SMN2 Q16637 2/20 0.48
▸ HSP90AA1 P07900 2/20 0.48
▸ ALOX15 P16050 2/20 0.48
▸ CCR1 P32246 2/20 0.48
▸ CCR5 P51681 2/20 0.48
▸ CCR8 P51685 2/20 0.48
▸ GMNN O75496 1/20 0.48
▸ TP53 P04637 1/20 0.48
▸ MMP2 P08253 1/20 0.48
▸ CYP2D6 P10635 1/20 0.48
▸ MMP9 P14780 1/20 0.48
▸ TSHR P16473 1/20 0.48
▸ NFKB1 P19838 1/20 0.48
▸ MMP8 P22894 1/20 0.48

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 SCHEMBL28806456 0.97 LMNA (0.77) LMNACYP3A4KDM4EMAPTHTT
Sulfuric Acid SCHEMBL3271974 0.97 LMNA (0.77) LMNACYP3A4KDM4EMAPTHTT
Hydrochloric Acid SCHEMBL27811005 0.89 LMNA (0.96) LMNACYP3A4KDM4EMAPTHTT
Sulfuric Acid SCHEMBL11132378 0.88 LMNA (0.79) LMNACYP3A4KDM4EMAPTHTT
Bromide SCHEMBL28796063 0.88 LMNA (0.92) LMNACYP3A4KDM4EMAPTHTT
SCHEMBL6513577 0.88 LMNA (1.00) LMNACYP3A4KDM4EMAPTHTT
SCHEMBL8313 0.88 LMNA (1.00) LMNACYP3A4KDM4EMAPTHTT
Trifluoromethanesulfonic Acid SCHEMBL6799589 0.86 LMNA (0.66) LMNACYP3A4KDM4EMAPTHTT
SCHEMBL28527433 0.86 LMNA (0.89) LMNACYP3A4KDM4EMAPTHTT
SCHEMBL1814141 0.86 LMNA (0.96) LMNACYP3A4KDM4EMAPTHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0646180-B1 METHODS FOR INACTIVATING NUCLEOTIDE SEQUENCES AND METAL CHELATES FOR USE THEREIN ABBOTT LAB (US) 2002-02-27 — — EP disclosed
US-5858650-A BLOCKING POLYMERASE, LIPASE CHAIN REACTION ABBOTT LABORATORIES (US) 1999-01-12 — — US disclosed
EP-0646180-A4 METHODS FOR INACTIVATING NUCLEOTIDE SEQUENCES AND METAL CHELATES FOR USE THEREIN. ABBOTT LAB (US) 1998-03-11 — — EP disclosed
EP-0646180-A1 METHODS FOR INACTIVATING NUCLEOTIDE SEQUENCES AND METAL CHELATES FOR USE THEREIN ABBOTT LABORATORIES (US) 1995-04-05 — — EP disclosed
WO-1993020241-A1 METHODS FOR INACTIVATING NUCLEOTIDE SEQUENCES AND METAL CHELATES FOR USE THEREIN ABBOTT LABORATORIES (US) 1993-10-14 — — WO disclosed
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