Tenofovir Alafenamide

Tenofovir Alafenamide

SCHEMBL16280324

CC(C)OC(=O)[C@H](C)N[P@](=O)(COC(C)Cn1cnc2c(N)ncnc21)Oc1ccccc1

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

pol

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
FAP Q12884 2/20 0.60
CYP3A4 P08684 14/20 0.58
CYP2D6 P10635 14/20 0.50
BTN3A1 O00481 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
Tenofovir Alafenamide SCHEMBL16402708 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL20456396 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL14440384 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL13155662 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL3107149 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL3107144 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL20456397 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL19467840 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL22139335 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1
Tenofovir Alafenamide SCHEMBL13964717 1.00 FAP (0.60) FAPCYP3A4CYP2D6BTN3A1

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.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2017118928-A9 PROCESS FOR THE SEPARATION OF DIASTEREOMERS OF TENOFOVIR ALAFENAMIDE LUPIN LIMITED (IN) 2017-12-07 WO disclosed
WO-2017118928-A9 PROCESS FOR THE SEPARATION OF DIASTEREOMERS OF TENOFOVIR ALAFENAMIDE LUPIN LIMITED (IN) 2017-12-07 WO disclosed
WO-2017118928-A1 PROCESS FOR THE SEPARATION OF DIASTEREOMERS OF TENOFOVIR ALAFENAMIDE LUPIN LIMITED (IN) 2017-07-13 WO disclosed
WO-2017118928-A1 PROCESS FOR THE SEPARATION OF DIASTEREOMERS OF TENOFOVIR ALAFENAMIDE LUPIN LIMITED (IN) 2017-07-13 WO disclosed
US-9676803-B2 Efficient process for separation of diastereomers of 9-[(R)-2-[[(R,S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl]methoxy]propyl]adenine CIPLA LIMITED (IN) 2017-06-13 US disclosed
US-9676803-B2 Efficient process for separation of diastereomers of 9-[(R)-2-[[(R,S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl]methoxy]propyl]adenine CIPLA LIMITED (IN) 2017-06-13 US disclosed
US-9676803-B2 Efficient process for separation of diastereomers of 9-[(R)-2-[[(R,S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl]methoxy]propyl]adenine CIPLA LIMITED (IN) 2017-06-13 US disclosed
US-20160122373-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL] METHOXY]PROPYL]ADENINE CIPLA LIMITED (IN) 2016-05-05 US disclosed
US-20160122373-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL] METHOXY]PROPYL]ADENINE CIPLA LIMITED (IN) 2016-05-05 US disclosed
EP-3004121-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL]METHOXY]PROPYL]ADENINE Cipla Limited (IN) 2016-04-13 EP disclosed
EP-3004121-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL]METHOXY]PROPYL]ADENINE Cipla Limited (IN) 2016-04-13 EP disclosed
EP-3004121-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL]METHOXY]PROPYL]ADENINE Cipla Limited (IN) 2016-04-13 EP disclosed
WO-2014195724-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL] METHOXY]PROPYL]ADENINE CIPLA LIMITED (IN) 2014-12-11 WO disclosed
WO-2014195724-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL] METHOXY]PROPYL]ADENINE CIPLA LIMITED (IN) 2014-12-11 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 (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-20160122373-A1 AN EFFICIENT PROCESS FOR SEPARATION OF DIASTEREOMERS OF 9-[(R)-2-[[(R,S)-[[(S)-1-(ISOPROPOXYCARBONYL)ETHYL]AMINO]-PHENOXYPHOSPHINYL] METHOXY]PROPYL]ADENINE MTAP, PARP9, APRT FAP 1817/4885CYP3A4 758/4885CYP2D6 775/4885

“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.