Lansoprazole

Lansoprazole

SCHEMBL1269346

Cc1c(OCC(F)(F)F)ccnc1C[S+]([O-])c1nc2ccccc2[nH]1.Cc1c(OCC(F)(F)F)ccnc1C[S+]([O-])c1nc2ccccc2[nH]1.S

nearest known ligand 0.62

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ATP4AATP4B

The experimentally established mechanism targets of Lansoprazole. 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
ATP4A known ✓ P20648 4/20 0.60
ATP4B known ✓ P51164 4/20 0.60
CYP2C9 P11712 4/20 0.62
NPC1 O15118 3/20 0.62
RAB9A P51151 3/20 0.62
CYP1A2 P05177 2/20 0.62
CYP3A4 P08684 2/20 0.62
CYP2D6 P10635 2/20 0.62
CYP2C19 P33261 2/20 0.62
MAPT P10636 4/20 0.60
WDR5 P61964 3/20 0.60
KMT2A Q03164 3/20 0.60
ENGASE Q8NFI3 3/20 0.60
SARM1 Q6SZW1 3/20 0.60
ALDH1A1 P00352 3/20 0.60
ATP1A1 P05023 3/20 0.60
ATP1B1 P05026 3/20 0.60
ATP1A3 P13637 3/20 0.60
ATP1B2 P14415 3/20 0.60
ATP1A2 P50993 3/20 0.60

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 SCHEMBL17956714 1.00 CYP2C9 (0.62) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Lansoprazole SCHEMBL29358567 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Dexlansoprazole SCHEMBL29750802 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Dexlansoprazole SCHEMBL29950208 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Lansoprazole SCHEMBL8597994 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Lansoprazole SCHEMBL22366 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Dexlansoprazole SCHEMBL29353881 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Lansoprazole SCHEMBL1559598 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Dexlansoprazole SCHEMBL44975 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4
Dexlansoprazole SCHEMBL29598842 0.99 CYP2C9 (0.63) CYP2C9NPC1RAB9ACYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118530954-A Polycyclic ketone monooxygenase mutant and application thereof in chiral azole drug synthesis 福州大学 2024-08-23 CN claimed
US-20220016099-A1 BENZIMIDAZOLE OR BENZOXAZOLE DERIVATIVES FOR PREVENTING AND TREATING CENTRAL NERVOUS SYSTEM DISEASE, DIABETES, AND COMPLICATIONS THEREOF TRINUERO (KR) 2022-01-20 US claimed
CN-113582973-A Preparation method of thioether 丽珠医药集团股份有限公司 2021-11-02 CN claimed
CN-112939941-A Preparation method of lansoprazole 珠海润都制药股份有限公司 2021-06-11 CN claimed
CN-109467527-B Tartrate thioester compound and preparation method and application thereof 江苏奥赛康药业有限公司 2021-04-06 CN claimed
WO-2020116742-A1 BENZIMIDAZOLE OR BENZOXAZOLE DERIVATIVES FOR PREVENTING AND TREATING CENTRAL NERVOUS SYSTEM DISEASE, DIABETES, AND COMPLICATIONS THEREOF 주식회사 트리뉴로 2020-06-11 WO claimed
CN-110545815-A Medical application of cytochrome bc1 compound inhibitor BEIJING WEILANZHIYUAN MEDICAL TECH CO LTD 2019-12-06 CN claimed
CN-107365300-B A method of effectively removing impurity in Lansoprazole crude product 桂林华信制药有限公司 2019-08-02 CN claimed
CN-109467527-A Tartaric acid sulfur ester and its preparation method and application 江苏奥赛康药业股份有限公司 2019-03-15 CN claimed
CN-107556290-A A kind of Lansoprazole thioether monohydrate structure cell and preparation method thereof 陕西合成药业股份有限公司 2018-01-09 CN claimed
CN-107365300-A A kind of method for effectively removing impurity in Lansoprazole crude product 桂林华信制药有限公司 2017-11-21 CN claimed
CN-106946849-A A kind of R-lansoprazole and preparation method thereof and purposes 乐普药业科技有限公司 2017-07-14 CN claimed
EP-2521531-B1 SKIN LIGHTENING COMPOSITIONS ELC MAN LLC (US) 2017-07-12 EP claimed
CN-106518847-A Oxidation method for Dexlansoprazole 李景丕 2017-03-22 CN claimed
WO-2008001392-A2 AN IMPROVED PROCESS FOR THE PREPARATION OF PANTOPRAZOLE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS MSN LABORATORIES LIMITED (IN) 2008-01-03 WO claimed
WO-2007138468-A2 PROCESSES FOR THE PREPARATION OF LANSOPRAZOLE WOCKHARDT LTD (IN) 2007-12-06 WO claimed
CN-118530954-A Polycyclic ketone monooxygenase mutant and application thereof in chiral azole drug synthesis 福州大学 2024-08-23 CN disclosed
US-20240238264-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF DISARM THERAPEUTICS, INC. 2024-07-18 US disclosed
WO-2004080440-A1 PROCESS FOR THE PREPARING OF HARDCAPSULE FORMULATION CONTAINING LANSOPRAZOLE KOREA UNITED PHARM, INC. (KR) 2004-09-23 WO disclosed
WO-2004056803-A1 PROCESS FOR THE PREPARATION OF SULPHINYL DERIVATIVES BY OXIDATION OF THE CORRESPONDING SULFIDES CHEMI SPA (IT) 2004-07-08 WO 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 (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-20240238264-A1 INHIBITORS OF SARM1 NADASE ACTIVITY AND USES THEREOF SARM1, NADK, NNMT ATP4A 3164/4885ATP4B 3335/4885CYP2C9 4424/4885
US-20220016099-A1 BENZIMIDAZOLE OR BENZOXAZOLE DERIVATIVES FOR PREVENTING AND TREATING CENTRAL NERVOUS SYSTEM DISEASE, DIABETES, AND COMPLICATIONS THEREOF KEAP1, SLC5A1, GCLC ATP4A 484/4885ATP4B 844/4885CYP2C9 1053/4885

“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.