Tenofovir Anhydrous

Tenofovir Anhydrous

SCHEMBL901180

C[C@H](Cn1cnc2c(N)ncnc21)OCP(=O)(O)O.O=P(O)(O)O

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

Ppol

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

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 15/20 0.98
CYP2D6 P10635 14/20 0.68
FAP Q12884 1/20 0.64

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
Tenofovir Anhydrous SCHEMBL3967109 1.00 CYP3A4 (0.98) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL400718 1.00 CYP3A4 (0.98) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL20295138 1.00 CYP3A4 (0.98) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL19586794 1.00 CYP3A4 (0.98) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL39724 0.99 CYP3A4 (1.00) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL497725 0.99 CYP3A4 (1.00) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL29355255 0.99 CYP3A4 (1.00) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL2040329 0.99 CYP3A4 (1.00) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL18894359 0.99 CYP3A4 (1.00) CYP3A4CYP2D6FAP
Tenofovir Anhydrous SCHEMBL18492311 0.98 CYP3A4 (0.98) CYP3A4CYP2D6FAP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107011382-A A kind of tenofovir prodrug and preparation method thereof 单爱莲 2017-08-04 CN claimed
WO-2025151774-A1 TREATING INFLAMMATORY RESPONSES THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2025-07-17 WO disclosed
US-11826375-B2 Phosphinic amide prodrugs of tenofovir MERCK SHARP & DOHME LLC (US) 2023-11-28 US disclosed
US-20220143050-A1 mTOR Inhibitor MURATA, Kazumoto (JP) 2022-05-12 US disclosed
EP-3559011-B1 ANTIVIRAL ESTER PRODRUGS OF TENOFOVIR MERCK SHARP & DOHME (US) 2022-04-13 EP disclosed
EP-3954389-A1 MTOR INHIBITOR Murata, Kazumoto (JP) 2022-02-16 EP disclosed
CN-113683641-A Tenofovir phosphate crystal form d and preparation and application thereof 西安新通药物研究股份有限公司 2021-11-23 CN disclosed
CN-113683641-A Tenofovir phosphate crystal form d and preparation and application thereof 西安新通药物研究股份有限公司 2021-11-23 CN disclosed
CN-113683641-A Tenofovir phosphate crystal form d and preparation and application thereof 西安新通药物研究股份有限公司 2021-11-23 CN disclosed
CN-113583049-A Tenofovir phosphate e crystal form and preparation and application thereof 西安新通药物研究股份有限公司 2021-11-02 CN disclosed
CN-104903334-B Tenofovir prodrug and application thereof in medicine 江苏豪森药业集团有限公司 2017-03-15 CN disclosed
CN-106188139-A Tenofovir list benzyl ester phosphoamide prodrug, its preparation method and application 江苏天士力帝益药业有限公司 2016-12-07 CN disclosed
CN-104903334-A Tenofovir prodrug and application thereof in medicine JIANGSU HANSOH PHARMACEUTICAL 2015-09-09 CN disclosed
US-20150225433-A1 TENOFOVIR PRODRUG AND PHARMACEUTICAL USES THEREOF JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2015-08-13 US disclosed
EP-2891658-A1 TENOFOVIR PRODRUG AND PHARMACEUTICAL USES THEREOF Jiangsu Hansoh Pharmaceutical Co., Ltd. (CN) 2015-07-08 EP disclosed
WO-2013132314-A1 TENOFOVIR PHOSPHATE, PROCESSES FOR THE PREPARATION AND PHARMACEUTICAL COMPOSITION THEREOF LAURUS LABS PRIVATE LIMITED (IN) 2013-09-12 WO disclosed
WO-2013132314-A1 TENOFOVIR PHOSPHATE, PROCESSES FOR THE PREPARATION AND PHARMACEUTICAL COMPOSITION THEREOF LAURUS LABS PRIVATE LIMITED (IN) 2013-09-12 WO disclosed
WO-2012041015-A1 METHOD FOR PREPARING ACYCLIC NUCLEOSIDE MONOPHOSPHATE COMPOUND AS ANTIVIRAL DRUG 中国医学科学院医药生物技术研究所 (CN) 2012-04-05 WO disclosed
CN-1319520-C Liposome and lipid composite preparation of nucleoside phosphoric acid compound SHANGHAI COMM UNIVERSITY (CN) 2007-06-06 CN disclosed
CN-1679514-A Liposome and lipid composite preparation of nucleoside phosphoric acid compound UNIV SHANGHAI COMMUNICATION (CN) 2005-10-12 CN 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 (3 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-20220143050-A1 mTOR Inhibitor MTOR, RICTOR, RPTOR CYP3A4 602/4885CYP2D6 739/4885FAP 1685/4885
US-20150225433-A1 TENOFOVIR PRODRUG AND PHARMACEUTICAL USES THEREOF SLC10A1, HPRT1, SLC5A1 CYP3A4 35/4885CYP2D6 14/4885FAP 414/4885
US-11826375-B2 Phosphinic amide prodrugs of tenofovir TYMP, PPA1, PNP CYP3A4 1743/4885CYP2D6 2129/4885FAP 436/4885

“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.