Lansoprazole Sulfide

Lansoprazole Sulfide

SCHEMBL106519

Cc1c(OCC(F)(F)F)ccnc1CSc1nc2ccccc2[nH]1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 8/20 1.00
NPC1 O15118 7/20 1.00
CYP1A2 P05177 3/20 1.00
CYP2D6 P10635 3/20 1.00
CYP2C9 P11712 3/20 1.00
CYP2C19 P33261 3/20 1.00
CYP3A4 P08684 2/20 1.00
KMT2A Q03164 5/20 0.63
MAPT P10636 5/20 0.63
LMNA P02545 3/20 0.63
WDR5 P61964 2/20 0.63
ENGASE Q8NFI3 2/20 0.63
CYP2C8 P10632 2/20 0.63
ALOX15 P16050 2/20 0.63
TSHR P16473 2/20 0.63
HSD17B10 Q99714 2/20 0.63
ALDH1A1 P00352 2/20 0.63
HPGD P15428 2/20 0.63
SARM1 Q6SZW1 1/20 0.63
KDM4E B2RXH2 1/20 0.63

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
Lansoprazole Sulfide SCHEMBL30053816 1.00 RAB9A (1.00) RAB9ANPC1CYP1A2CYP2D6CYP2C9
Lansoprazole Sulfide SCHEMBL6948284 0.99 RAB9A (0.98) RAB9ANPC1CYP1A2CYP2D6CYP2C9
Lansoprazole Sulfide SCHEMBL1680900 0.99 RAB9A (0.98) RAB9ANPC1CYP1A2CYP2D6CYP2C9
Lansoprazole Sulfide SCHEMBL1681186 0.99 RAB9A (0.98) RAB9ANPC1CYP1A2CYP2D6CYP2C9
Lansoprazole Sulfide SCHEMBL1681462 0.95 RAB9A (0.90) RAB9ANPC1CYP1A2CYP2D6CYP2C9
Lansoprazole Sulfide SCHEMBL8184520 0.94 RAB9A (0.89) RAB9ANPC1CYP1A2CYP2D6CYP2C9
SCHEMBL29323856 0.93 RAB9A (0.86) RAB9ANPC1CYP1A2CYP2D6CYP2C9
SCHEMBL6440543 0.92 RAB9A (0.85) RAB9ANPC1CYP1A2CYP2D6CYP2C9
Water SCHEMBL6737292 0.91 RAB9A (0.83) RAB9ANPC1CYP1A2CYP2D6CYP2C9
Water SCHEMBL6737289 0.91 RAB9A (0.83) RAB9ANPC1CYP1A2CYP2D6CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114163419-A Preparation method of lansoprazole 辰欣药业股份有限公司 2022-03-11 CN claimed
CN-111714639-A Composition comprising histamine release-promoting substance and benzimidazole derivative 黄泳华 2020-09-29 CN claimed
CN-111084886-A Composition comprising fatty acid or derivative thereof and benzimidazole derivative 黄泳华 2020-05-01 CN claimed
US-9228216-B2 Synthesis of prazole compounds CODEXIS, INC. (US) 2016-01-05 US claimed
US-20150056668-A1 SYNTHESIS OF PRAZOLE COMPOUNDS INNOVATUS LIFE SCIENCES LENDING FUND I, LP, AS COLLATERAL AGENT 2015-02-26 US claimed
US-20130012714-A1 NOVEL SOLVATE OF DEXLANSOPRAZOLE ORCHID CHEMICALS & PHARMACEUTICALS LIMITED (IN) 2013-01-10 US claimed
EP-2510089-A2 SYNTHESIS OF PRAZOLE COMPOUNDS Codexis, Inc. (US) 2012-10-17 EP claimed
US-8039631-B2 Process for preparing crystalline form A of Lansoprazole DAEWOONG PHARMACEUTICAL CO., LTD. (KR) 2011-10-18 US claimed
WO-2011098938-A1 NOVEL SOLVATE OF DEXLANSOPRAZOLE ORCHID CHEMICALS AND PHARMACEUTICALS LIMITED (IN) 2011-08-18 WO claimed
WO-2011071982-A2 SYNTHESIS OF PRAZOLE COMPOUNDS CODEXIS, INC. (US) 2011-06-16 WO claimed
US-6603009-B2 Oxidation of a thioether to a sulfoxide using sodium percarbonate and a molybdenum salt as catalyst; making lansoprazole, omeprazole, rabeprazole, and pantoprazole ESTEVE QUIMICA, S.A. (ES) 2003-08-05 US claimed
US-20030028030-A1 Method for oxidizing a thioether group into a sulfoxide group ESTEVE QUIMICA, S.A. (ES) 2003-02-06 US claimed
EP-1270555-A1 METHOD FOR OXIDIZING A THIOETHER GROUP INTO A SULFOXIDE GROUP ESTEVE QUIMICA, S.A. (ES) 2003-01-02 EP claimed
WO-2000078729-A1 CRYSTALLINE FORMS OF LANSOPRAZOLE INSTYTUT FARMACEUTYCZNY (PL) 2000-12-28 WO claimed
WO-2000027841-A1 METHOD OF PREPARING SULFIDE DERIVATIVES DONG-A PHARMACEUTICAL CO., LTD. (KR) 2000-05-18 WO claimed
US-5578732-A MONO-OXIDATION OF SULFUR ATOM BY HYDROGEN PEROXIDE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1996-11-26 US claimed
EP-0382489-B1 Use of benzimidazole derivatives as antibacterial agents TAKEDA CHEMICAL INDUSTRIES LTD (JP) 1994-11-17 EP claimed
US-5013743-A Use of substituted pyridylmethylsulfinyl- and pyridylmethylthiobenzimidazoles such as lansoprazole, 2-(3-methyl-4-(2,2,2-trifluoroethoxy)pyrid-2-yl)methylthiobenzimidazole TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1991-05-07 US claimed
EP-0382489-A2 Use of benzimidazole derivatives as antibacterial agents Takeda Chemical Industries, Ltd. (JP) 1990-08-16 EP claimed
US-4628098-A Including Prevacid (TM) lansoprazole, 2-(3-methyl-4-(2,2,2-trifluoroethoxy)-5-methyl-pyrid-2 -yl)methylsulfinylbenzimidazole; proton pump inhibitors, antiulcer, antisecretory agents TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1986-12-09 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20030028030-A1 Method for oxidizing a thioether group into a sulfoxide group CBR1, CBR3, SCO2 RAB9A 2297/4885NPC1 1435/4885CYP1A2 2157/4885
US-20130012714-A1 NOVEL SOLVATE OF DEXLANSOPRAZOLE CYP2D6, CYP2S1, CYP2F1 RAB9A 1039/4885NPC1 4592/4885CYP1A2 46/4885

“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.