Pf-232798

Pf-232798

SCHEMBL3075846

CC(=O)N[C@@H](CCN1C2CCC1CC(n1c(C)nc3c1CCN(C(=O)C(C)C)C3)C2)c1cccc(F)c1.O=C(O)/C=C/C(=O)O

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CCR5

The experimentally established mechanism targets of Pf-232798. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
▸ CCR5 known ✓ P51681 12/20 0.92
▸ KCNH2 Q12809 8/20 0.92

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
Pf-232798 SCHEMBL3075843 1.00 CCR5 (0.92) CCR5KCNH2
Pf-232798 SCHEMBL1049072 0.96 CCR5 (1.00) CCR5KCNH2
Pf-232798 SCHEMBL1527455 0.96 CCR5 (1.00) CCR5KCNH2
Pf-232798 SCHEMBL30227242 0.96 CCR5 (1.00) CCR5KCNH2
Pf-232798 SCHEMBL14700573 0.96 CCR5 (1.00) CCR5KCNH2
Pf-232798 SCHEMBL3071187 0.93 CCR5 (0.92) CCR5KCNH2
SCHEMBL30227452 0.91 CCR5 (0.89) CCR5KCNH2
SCHEMBL2575126 0.90 KCNH2 (0.90) CCR5KCNH2
SCHEMBL2575130 0.90 KCNH2 (0.90) CCR5KCNH2
SCHEMBL3070604 0.90 KCNH2 (1.00) CCR5KCNH2

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1682545-B1 IMIDAZOPYRIDINE SUBSTITUTED TROPANE DERIVATIVES WITH CCR5 RECEPTOR ANTAGONIST ACTIVITY FOR THE TREATMENT OF HIV AND INFLAMMATION PFIZER LTD (GB) 2007-12-12 — — EP claimed
US-7790740-B2 Imidazopyridine substituted tropane derivatives with CCR5 receptor antagonist activity for the treatment of HIV and inflammation PFIZER INC (US) 2010-09-07 — — US disclosed
US-20080045563-A1 IMIDAZOPYRIDINE SUBSTITUTED TROPANE DERIVATIVES WITH CCR5 RECEPTOR ANTAGONIST ACTIVITY FOR THE TREATMENT OF HIV AND INFLAMMATION PFIZER INC. 2008-02-21 — — US disclosed
US-7309790-B2 Chemical compounds PFIZER INC (US) 2007-12-18 — — US disclosed
EP-1682545-B1 IMIDAZOPYRIDINE SUBSTITUTED TROPANE DERIVATIVES WITH CCR5 RECEPTOR ANTAGONIST ACTIVITY FOR THE TREATMENT OF HIV AND INFLAMMATION PFIZER LTD (GB) 2007-12-12 — — EP disclosed
US-20050131011-A1 Chemical compounds PFIZER, INC. 2005-06-16 — — 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 (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-20080045563-A1 IMIDAZOPYRIDINE SUBSTITUTED TROPANE DERIVATIVES WITH CCR5 RECEPTOR ANTAGONIST ACTIVITY FOR THE TREATMENT OF HIV AND INFLAMMATION CCR5, CCR2, CX3CR1 CCR5 1/4885KCNH2 2405/4885
US-20050131011-A1 Chemical compounds CCR5, CCR2, CX3CR1 CCR5 1/4885KCNH2 3565/4885

“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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