Lithium

Lithium

SCHEMBL586148

[Li].c1ccc(COCc2ccccc2)cc1

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 1/20 0.94
▸ IDO1 P14902 1/20 0.57
▸ AGXT P21549 1/20 0.55
▸ CA1 P00915 5/20 0.50
▸ CA2 P00918 3/20 0.50
▸ CA9 Q16790 3/20 0.50
▸ CA7 P43166 2/20 0.50
▸ KDM4E B2RXH2 1/20 0.50
▸ POLB P06746 1/20 0.50
▸ TACR1 P25103 2/20 0.48
▸ CALM1 P0DP23 1/20 0.47
▸ ALDH1A1 P00352 2/20 0.46
▸ LMNA P02545 1/20 0.46
▸ CYP1A2 P05177 1/20 0.46
▸ PTGS1 P23219 1/20 0.46
▸ SLC6A2 P23975 1/20 0.46
▸ CYP2C19 P33261 1/20 0.46
▸ PTGS2 P35354 1/20 0.46
▸ SLC6A3 Q01959 1/20 0.46
▸ HIF1A Q16665 1/20 0.46

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
SCHEMBL5311581 0.97 TSHR (1.00) TSHRIDO1AGXTCA1CA2
SCHEMBL27380 0.97 TSHR (1.00) TSHRIDO1AGXTCA1CA2
Water SCHEMBL15535487 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2
SCHEMBL9491202 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2
Potassium SCHEMBL586337 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2
SCHEMBL574533 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2
Ammonia Solution, Strong SCHEMBL8645051 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2
Barium SCHEMBL3798966 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2
Hydrochloric Acid SCHEMBL11878622 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2
Water SCHEMBL10609439 0.94 TSHR (0.94) TSHRIDO1AGXTCA1CA2

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 102 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0525880-B1 Catalytic alkylation process FMC CORP (US) 1998-05-06 — — EP claimed
US-5332853-A Alkylating tetrachlorosilane or an alkylchlorosilane with an alkyllithium using ether, metal alkoxide, amine, or metal amide as catalyst FMC CORPORATION (US) 1994-07-26 — — US claimed
EP-0525880-A1 Catalytic alkylation process FMC CORPORATION (US) 1993-02-03 — — EP claimed
US-4051320-A PROCESS FOR PREPARING ALKOXYLATED DERIVATIVES OF CEPHALOSPORIN COMPOUNDS SANKYO COMPANY LIMITED (JA) 1977-09-27 — — US claimed
EP-3587490-B1 METHACRYLIC RESIN COMPOSITION AND USE THEREOF KURARAY CO (JP) 2022-10-12 — — EP disclosed
US-11299600-B2 Methacrylic resin composition and use thereof KURARAY CO., LTD. (JP) 2022-04-12 — — US disclosed
US-20210077420-A1 Methods of Treatment of Gout HOOPER MARK (GB) 2021-03-18 — — US disclosed
US-20200377688-A1 METHACRYLIC RESIN COMPOSITION AND USE THEREOF KURARAY CO., LTD. (JP) 2020-12-03 — — US disclosed
EP-3723741-A1 DISSOLUTION OF MONOSODIUM URATE TO TREAT GOUT Hooper, Mark (GB) 2020-10-21 — — EP disclosed
WO-2019116045-A1 DISSOLUTION OF MONOSODIUM URATE TO TREAT GOUT HOOPER MARK (GB) 2019-06-20 — — WO disclosed
US-8119749-B2 Method of taking (meth)acrylic ester polymer out of liquid reaction mixture KURARAY CO., LTD. (JP) 2012-02-21 — — US disclosed
EP-1916262-B1 METHOD OF TAKING (METH)ACRYLIC ESTER POLYMER OUT OF LIQUID REACTION MIXTURE KURARAY CO (JP) 2012-02-15 — — EP disclosed
EP-0279463-A2 Graft polymerization of substituted styrene polymers having pendant vinylidene groups Nippon Paint Co., Ltd. (JP) 1988-08-24 — — EP disclosed
US-4525309-A Lewis acid catalysis of the homologation of boronic esters with haloalkylmetal reagents WASHINGTON STATE UNIVERSITY RESEARCH FOUNDATION, INC. (US) 1985-06-25 — — US disclosed
US-4145540-A ANTIBIOTICS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1979-03-20 — — US disclosed
US-4051320-A PROCESS FOR PREPARING ALKOXYLATED DERIVATIVES OF CEPHALOSPORIN COMPOUNDS SANKYO COMPANY LIMITED (JA) 1977-09-27 — — US disclosed
US-4048160-A Process for preparation of 7-alkoxy-3-bromomethylcephems ELI LILLY AND COMPANY (US) 1977-09-13 — — US disclosed
US-4048163-A Process for preparation of 7-alkoxy-3-chloromethylcephems ELI LILLY AND COMPANY (US) 1977-09-13 — — US disclosed
US-4044000-A Substituted β-lactam antibiotics ELI LILLY AND COMPANY (US) 1977-08-23 — — US disclosed
US-3994885-A WITH ALKALI METAL ALKOXIDE, HALOGENATION ELI LILLY AND COMPANY (US) 1976-11-30 — — 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-20210077420-A1 Methods of Treatment of Gout XDH, SLC10A1, LIPA TSHR 3963/4885IDO1 4149/4885AGXT 240/4885

“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.

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