Water — predicted protein targets

Known targets — ChEMBL curated mechanism

ABCC9 ABL1 ACE ACHE ACVR1 ADORA1 ADORA2A ADORA2B ADORA3 ADRA1A ADRA1B ADRA1D ADRA2A ADRA2B ADRA2C ADRB1 ADRB2 ADRB3 AGTR1 ALOX5 ATP4A ATP4B BCR BTK CACNA1A CACNA1B CACNA1C CACNA1D CACNA1E CACNA1F CACNA1G CACNA1H CACNA1I CACNA1S CACNA2D1 CACNA2D2 CACNA2D3 CACNA2D4 CACNB1 CACNB2 CACNB3 CACNB4 CACNG1 CACNG2 CACNG3 CACNG4 CACNG5 CACNG6 CACNG7 CACNG8 CALCRL CFB CHRM1 CHRM2 CHRM3 CHRM4 CHRM5 CHRNA1 CHRNB1 CHRND CHRNE CHRNG CRBN CUL4A CXCR1 CXCR2 DDB1 DDC DHFR DPP4 DRD2 DRD3 DRD4 EGFR ERBB2 ERBB4 ESR1 ESR2 FDPS FKBP1A FLT1 FLT3 FLT4 GART GHSR GRIA1 GRIA2 GRIA3 GRIA4 GRIK1 GRIK2 GRIK3 GRIK4 GRIK5 GRIN2A GSK3A GSK3B HDAC1 HDAC10 HDAC11 HDAC2 HDAC3 HDAC4 HDAC5 HDAC6 HDAC7 HDAC8 HDAC9 HRH1 HTR1A HTR1B HTR1D HTR1E HTR1F HTR2A HTR2B HTR2C HTR3A HTR3B HTR3C HTR3D HTR3E HTR4 HTR5A HTR6 HTR7 IDH1 IDH2 IMPA1 ITGA2B ITGB3 JAK1 JAK2 JAK3 KCNJ11 KCNK3 KCNK9 KDR KIT MEN1 MET MMP1 MMP13 MMP7 MMP8 NA NOD2 NS5b ODC1 OPG057 OPRD1 OPRK1 OPRM1 P PARP1 PARP2 PDE3A PDE3B PDE4A PDE4B PDE4C PDE4D PDGFRB PIK3CA PIK3CB PIK3CD PIK3CG PIK3R1 PIK3R2 PIK3R3 PIK3R5 PKLR PPARD PPAT PTGS1 PTGS2 RBX1 ROCK1 ROCK2 RRM1 RRM2 RRM2B SCN10A SCN11A SCN1A SCN2A SCN3A SCN4A SCN5A SCN7A SCN8A SCN9A SCNN1A SCNN1B SCNN1G SIGMAR1 SLC10A2 SLC5A2 SLC6A2 SLC6A3 SLC6A4 SLC9A3 SYK TACR1 THRA THRB TOP1 TUBA1A TUBA1B TUBA1C TUBA3C TUBA3E TUBA4A TUBB TUBB1 TUBB2A TUBB2B TUBB3 TUBB4A TUBB4B TUBB6 TUBB8 TYK2 TYMS VDR ampC bla blaT-3 blaT-4 blaT-5 blaT-6 blaUOE-1 dacA dacB dacC folA folP ftsI gyrA gyrB ileS mecA mrcA mrcB mrdA parC parE pbp2 pbp4 pbpA pbpF 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 rpmC rpmD rpmE rpmE2 rpmF rpmG rpmG1 rpmG2 rpmG3 rpmH rpmI rpmJ rpsA rpsB rpsC rpsD rpsE rpsF rpsG rpsH rpsI rpsJ rpsK rpsL rpsM rpsN rpsO rpsP rpsQ rpsR rpsS rpsT rpsU thyA ykgM ykgO

The experimentally established mechanism targets of Water. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

	gene	UniProt	supporting neighbours	confidence
▸	SLC6A4 known ✓	P31645	1/20	0.37

▸	MEN1 known ✓	O00255	2/20	0.35

▸	KDM4E	B2RXH2	4/20	0.40

▸	KMT2A	Q03164	3/20	0.40

▸	L3MBTL1	Q9Y468	1/20	0.40

▸	ALDH1A1	P00352	4/20	0.37

▸	CYP1A2	P05177	2/20	0.37

▸	CYP2C19	P33261	2/20	0.37

▸	CYP2C9	P11712	1/20	0.37

▸	CNR1	P21554	3/20	0.35

▸	CNR2	P34972	3/20	0.35

▸	NPC1	O15118	3/20	0.35

▸	GAA	P10253	3/20	0.35

▸	HTT	P42858	3/20	0.35

▸	RAB9A	P51151	3/20	0.35

▸	SMN1; SMN2	Q16637	3/20	0.35

▸	NPSR1	Q6W5P4	2/20	0.35

▸	LMNA	P02545	1/20	0.35

▸	CYP2D6	P10635	1/20	0.35

▸	HPGD	P15428	1/20	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
Hydrochloric Acid SCHEMBL9516629	0.97	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Water SCHEMBL11439162	0.86	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Water SCHEMBL11433319	0.86	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Water SCHEMBL11428305	0.86	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Water SCHEMBL11433831	0.86	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Water SCHEMBL11430549	0.86	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Water SCHEMBL11427301	0.86	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Hydrochloric Acid SCHEMBL9347038	0.84	KDM4E (0.39)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Hydrochloric Acid SCHEMBL11127238	0.83	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1
Hydrochloric Acid SCHEMBL11129284	0.83	KDM4E (0.40)	KDM4EKMT2AL3MBTL1SLC6A4ALDH1A1

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.

Patent	Title	Assignee	Published	Priority	Filing	Country	Status
US-5401390-A	Oxidation of mercaptans to disulfides	UOP (US)	1995-03-28	—	—	US	disclosed
EP-0499743-B1	Two step process for sweetening a sour hydrocarbon fraction	UOP INC (US)	1994-07-20	—	—	EP	disclosed
US-5318936-A	Metal chelate dispersed on catalyst support; layered double hydroxide; for oxidizing mercaptans to disulfides	UOP (US)	1994-06-07	—	—	US	disclosed
US-5286372-A	Catalyst is composed of metal chelate dispersed on basic support which is either a solid solution of metal oxides or a layered double hydroxide	UOP (US)	1994-02-15	—	—	US	disclosed
US-5273646-A	Adding aqueous ammonium hydroxide, metal chelate and an onium compound to the hydrocarbon fraction containing an oxidizer and base	UOP (US)	1993-12-28	—	—	US	disclosed
US-5232887-A	Metal chelate diispersed on a metal oxide or layered double hydroxide support	UOP (US)	1993-08-03	—	—	US	disclosed
US-5204306-A	Oxidizing mercaptans to disulfides with metal chelate catalyst and an onium component	UOP (US)	1993-04-20	—	—	US	disclosed
US-5180484-A	Oxidation in presence of ammonium hydroxide, metal chelate and onium compound	UOP (US)	1993-01-19	—	—	US	disclosed
EP-0499743-A1	Two step process for sweetening a sour hydrocarbon fraction	UOP (US)	1992-08-26	—	—	EP	disclosed
US-5093296-A	Caustic free liquid/liquid process for sweetening a sour hydrocarbon fraction	UOP (US)	1992-03-03	—	—	US	disclosed
US-5064525-A	Catalysis; hydrogenation	UOP (US)	1991-11-12	—	—	US	disclosed
EP-0394571-A1	Use of a novel catalytic composite for sweetening of sour petroleum distillate	UOP (US)	1990-10-31	—	—	EP	disclosed
US-4913802-A	OXIDIZING MERCAPTAN TO DISULFIDES USING AMMONIUM HYDROXIDE AND A QUATERNARY AMMONIUM HYDROXIDE WITH CATALYTIC COMPOSITE	UOP (US)	1990-04-03	—	—	US	disclosed
US-4824818-A	OXIDATION CATALYST CONTAINING METAL CHELATE AND ONIUM COMPOUND	UOP INC. (US)	1989-04-25	—	—	US	disclosed