Sulfuric Acid

SCHEMBL6376476

NOC[C@]1(O[C@@H]2O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O.NOC[C@]1(O[C@@H]2O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O.O=S(=O)(O)O

nearest known ligand 0.57

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1A ADRA1B ADRA1D ADRA2A ADRA2B ADRA2C ADRB1 ADRB2 ADRB3 CALCRL CHRM1 CHRM2 CHRM3 F2R MAOA MAOB MAP2K1 MAP2K2 NTRK1 NTRK2 NTRK3 OPRD1 OPRK1 OPRM1 P2RY12 PKLR SCN10A SCN11A SCN1A SCN2A SCN3A SCN4A SCN5A SCN7A SCN8A SCN9A SLC18A2 SLC6A2 SLC6A3 TLR7 TLR9 TUBA1A TUBA1B TUBA1C TUBA3C TUBA3E TUBA4A TUBB TUBB1 TUBB2A TUBB2B TUBB3 TUBB4A TUBB4B TUBB6 TUBB8 dacA dacB dacC folA ftsI mrcA mrcB mrdA pol rplA rplB rplC rplD rplE rplF rplI rplJ rplK rplL rplM rplN rplO rplP rplQ rplR rplS rplT rplU rplV rplW rplX rplY rpmA rpmB rpmB1 rpmB2 rpmC rpmD rpmE rpmE2 rpmF rpmG rpmG1 rpmG2 rpmH rpmI rpmJ rpmJ2 rpsA rpsB rpsC rpsD rpsE rpsF rpsG rpsH rpsI rpsJ rpsK rpsL rpsM rpsN rpsO rpsP rpsQ rpsR rpsR1 rpsR2 rpsS rpsT rpsU rpsZ ykgM ykgO

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 13)

	gene	UniProt	supporting neighbours	confidence
▸	CDK1	P06493	1/20	0.57

▸	CCNB1	P14635	1/20	0.57

▸	CA2	P00918	8/20	0.46

▸	CA9	Q16790	4/20	0.46

▸	MAPT	P10636	1/20	0.39

▸	MEN1	O00255	1/20	0.39

▸	KMT2A	Q03164	1/20	0.39

▸	LDHA	P00338	1/20	0.39

▸	EPHX2	P34913	1/20	0.37

▸	TYR	P14679	1/20	0.36

▸	PTPN1	P18031	1/20	0.36

▸	CA1	P00915	6/20	0.35

▸	CA12	O43570	3/20	0.35

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.

Compound	similarity	top predicted	shared targets
SCHEMBL925520	0.94	CDK1 (0.63)	CDK1CCNB1CA2CA9MAPT
Bicarbonate SCHEMBL8355662	0.91	CDK1 (0.58)	CDK1CCNB1CA2CA9MAPT
Acetic Acid SCHEMBL190256	0.89	CDK1 (0.56)	CDK1CCNB1CA2CA9MAPT
Nitric Acid SCHEMBL6009046	0.88	CDK1 (0.55)	CDK1CCNB1CA2CA9MEN1
Sucrose SCHEMBL367818	0.87	CDK1 (0.73)	CDK1CCNB1CA2CA9MAPT
Sucrose SCHEMBL10405566	0.87	CDK1 (0.73)	CDK1CCNB1CA2CA9MAPT
SCHEMBL444151	0.86	CDK1 (0.58)	CDK1CCNB1CA2CA9MAPT
Sucrose SCHEMBL9704445	0.86	CDK1 (0.71)	CDK1CCNB1CA2CA9MAPT
Sucrose SCHEMBL9747719	0.86	CDK1 (0.71)	CDK1CCNB1CA2CA9MAPT
Sucrose SCHEMBL2065050	0.86	CDK1 (0.71)	CDK1CCNB1CA2CA9MAPT

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.

Patent	Title	Assignee	Published	Priority	Filing	Country	Status
US-20050124531-A1	Biological inhibitions induced by contact inhibitory factor	NEW YORK UNIVERSITY (US)	2005-06-09	—	—	US	disclosed
WO-2003072737-A2	BIOLOGICAL INHIBITIONS INDUCED BY CONTACT INHIBITORY FACTOR	NEW YORK UNIVERSITY (US)	2003-09-04	—	—	WO	disclosed