Vicriviroc

Vicriviroc

SCHEMBL15375740

COCC(c1ccc(C(F)(F)F)cc1)N1CCN(C2(C)CCN(C(=O)c3c(C)ncnc3C)CC2)C[C@@H]1C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CCR5

The experimentally established mechanism targets of Vicriviroc. 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
▸ CCR5 known ✓ P51681 20/20 1.00
▸ CHRM2 P08172 16/20 0.84
▸ CHRM1 P11229 4/20 0.84
▸ CHRM3 P20309 2/20 0.84

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
Vicriviroc SCHEMBL118885 1.00 CCR5 (1.00) CCR5CHRM2CHRM1CHRM3
Vicriviroc SCHEMBL4638191 1.00 CCR5 (1.00) CCR5CHRM2CHRM1CHRM3
Vicriviroc SCHEMBL4447817 1.00 CCR5 (1.00) CCR5CHRM2CHRM1CHRM3
Vicriviroc SCHEMBL29392831 0.96 CCR5 (0.91) CCR5CHRM2CHRM1CHRM3
SCHEMBL19656878 0.95 CCR5 (0.91) CCR5CHRM2CHRM1CHRM3
Vicriviroc SCHEMBL3321008 0.95 CCR5 (0.90) CCR5CHRM2CHRM1CHRM3
SCHEMBL14032029 0.92 CCR5 (0.85) CCR5CHRM2CHRM1CHRM3
SCHEMBL13484306 0.92 CCR5 (0.84) CCR5CHRM2CHRM1CHRM3
SCHEMBL15199622 0.91 CCR5 (1.00) CCR5CHRM2CHRM1CHRM3
SCHEMBL10073358 0.91 CCR5 (1.00) CCR5CHRM2CHRM1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12228580-B2 Methods of assigning a COVID pathological type based on a cytokine/chemokine panel INCELLDX, INC. (US) 2025-02-18 — — US disclosed
US-11952373-B2 Method of treating hypercytokinemia by administering the CCR5/CCL5 (RANTES) interaction inhibitor maraviroc INCELLDX, INC. (US) 2024-04-09 — — US disclosed
US-20240019447-A1 Methods of Assigning a COVID Pathological Type and Compositions for Practicing the Same, and Methods of Treating a Subject for Chronic COVID-19 INCELLDX, INC. 2024-01-18 — — US disclosed
US-20230364085-A1 USE OF MODULATORS OF CCR5 IN THE TREATMENT OF CANCER AND CANCER METASTASIS PESTELL RICHARD G (US) 2023-11-16 — — US disclosed
EP-4264280-A1 METHODS OF ASSIGNING A COVID PATHOLOGICAL TYPE AND COMPOSITIONS FOR PRACTICING THE SAME, AND METHODS OF TREATING A SUBJECT FOR CHRONIC COVID-19 IncellDx, Inc. (US) 2023-10-25 — — EP disclosed
US-11633397-B2 Use of modulators of CCR5 in the treatment of cancer and cancer metastasis PESTELL RICHARD G (US) 2023-04-25 — — US disclosed
US-11629196-B2 Method of treating SARS-CoV-2-associated hypercytokinemia by administering a human monoclonal antibody (PRO-140) that inhibits CCR5/CCL5 binding interactions INCELLDX, INC. (US) 2023-04-18 — — US disclosed
EP-4143235-A1 METHODS AND COMPOSITIONS FOR TREATING CYTOKINE STORM INFECTIONS, INCLUDING COVID-19, BY INHIBITING CCR5/CCL5 INTERACTION IncellDx, Inc. (US) 2023-03-08 — — EP disclosed
CN-115414480-A Dianhydrogalactitol in combination with radiation for treatment of non-small cell lung cancer and glioblastoma multiforme 德玛医药 2022-12-02 — — CN disclosed
US-20220317134-A1 Methods of Assigning a COVID Pathological Type and Compositions for Practicing the Same, and Methods of Treating a Subject for Chronic COVID-19 INCELLDX, INC. 2022-10-06 — — US disclosed
US-10301281-B2 Crystal forms of a CCR5 antagonist MERCK SHARP & DOHME CORP. (US) 2019-05-28 — — US disclosed
EP-3463373-A1 COMBINATION THERAPIES WITH FARNESOID X RECEPTOR (FXR) MODULATORS Akarna Therapeutics, Ltd. (GB) 2019-04-10 — — EP disclosed
US-20180303830-A1 CANCERS EXPRESSING CCR5 AND METHODS OF TREATMENT OF SAME THOMAS JEFFERSON UNIVERSITY (US) 2018-10-25 — — US disclosed
US-20170342053-A1 CRYSTAL FORMS OF A CCR5 ANTAGONIST MERCK SHARP & DOHME CORP. (US) 2017-11-30 — — US disclosed
WO-2017205684-A1 COMBINATION THERAPIES WITH FARNESOID X RECEPTOR (FXR) MODULATORS AKARNA THERAPEUTICS, LTD. (GB) 2017-11-30 — — WO disclosed
US-20170342053-A1 CRYSTAL FORMS OF A CCR5 ANTAGONIST MERCK SHARP & DOHME CORP. (US) 2017-11-30 — — US disclosed
US-20170231991-A1 Use Of Modulators Of CCR5 In The Treatment Of Cancer And Cancer Metastasis NIH-DEITR 2017-08-17 — — US disclosed
WO-2016209926-A1 CANCERS EXPRESSING CCR5 AND METHODS OF TREATMENT OF SAME THOMAS JEFFERSON UNIVERSITY (US) 2016-12-29 — — WO disclosed
US-9453836-B2 Use of modulators of CCR5 in the treatment of cancer and cancer metastasis PESTELL, RICHARD G. 2016-09-27 — — US disclosed
US-20130303512-A1 Use of modulators of CCR5 in the treatment of Cancer and cancer metastasis PESTELL, RICHARD G. 2013-11-14 — — 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-20170342053-A1 CRYSTAL FORMS OF A CCR5 ANTAGONIST CCR5, CCL5, CCR2 CCR5 1/4885CHRM2 421/4885CHRM1 207/4885
US-10301281-B2 Crystal forms of a CCR5 antagonist CCR5, CCL5, CCR2 CCR5 1/4885CHRM2 421/4885CHRM1 207/4885

“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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