Mavorixafor

Mavorixafor

SCHEMBL2511950

NCCCCN(Cc1nc2ccccc2[nH]1)[C@H]1CCCc2cccnc21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CXCR4

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

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
CXCR4 known ✓ P61073 20/20 1.00
CHRM2 P08172 1/20 1.00
CYP2D6 P10635 1/20 1.00
DRD2 P14416 1/20 1.00
OPRM1 P35372 1/20 1.00
KCNH2 Q12809 1/20 1.00
CYP3A4 P08684 1/20 0.73

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
Mavorixafor SCHEMBL29379072 1.00 CXCR4 (1.00) CXCR4CHRM2CYP2D6DRD2OPRM1
Mavorixafor SCHEMBL29932203 1.00 CXCR4 (1.00) CXCR4CHRM2CYP2D6DRD2OPRM1
Mavorixafor SCHEMBL4716578 1.00 CXCR4 (1.00) CXCR4CHRM2CYP2D6DRD2OPRM1
Mavorixafor SCHEMBL1288182 1.00 CXCR4 (1.00) CXCR4CHRM2CYP2D6DRD2OPRM1
Mavorixafor SCHEMBL29701264 1.00 CXCR4 (1.00) CXCR4CHRM2CYP2D6DRD2OPRM1
SCHEMBL2508418 0.99 CXCR4 (1.00) CXCR4CHRM2CYP2D6DRD2OPRM1
SCHEMBL2511014 0.99 CXCR4 (1.00) CXCR4CHRM2CYP2D6DRD2OPRM1
Mavorixafor SCHEMBL3798687 0.99 CXCR4 (0.98) CXCR4CHRM2CYP2D6DRD2OPRM1
SCHEMBL14131151 0.97 CXCR4 (0.95) CXCR4CHRM2CYP2D6DRD2OPRM1
SCHEMBL30096707 0.97 CXCR4 (0.95) CXCR4CHRM2CYP2D6DRD2OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1465889-B1 CHEMOKINE RECEPTOR BINDING HETEROCYCLIC COMPOUNDS WITH ENHANCED EFFICACY GENZYME CORP (US) 2017-03-22 EP claimed
EP-1730113-B1 PROCESS FOR THE SYNTHESIS OF A CXCR4 ANTAGONIST GENZYME CORP (US) 2016-12-28 EP claimed
US-8211879-B2 Cationic steroid antimicrobial compositions and methods of use BRIGHAM YOUNG UNIVERSITY (US) 2012-07-03 US claimed
US-20080167341-A1 CHEMOKINE RECEPTOR BINDING HETEROCYCLIC COMPOUNDS WITH ENHANCED EFFICACY GENZYME CORPORATION 2008-07-10 US claimed
US-7354934-B2 Chemokine receptor binding heterocyclic compounds with enhanced efficacy ANORMED, INC. (CA) 2008-04-08 US claimed
EP-1730113-A1 PROCESS FOR THE SYNTHESIS OF A CXCR4 ANTAGONIST ANORMED INC. (CA) 2006-12-13 EP claimed
WO-2005090308-A1 PROCESS FOR THE SYNTHESIS OF A CXCR4 ANTAGONIST ANORMED, INC. (CA) 2005-09-29 WO claimed
US-20050209277-A1 Process for the synthesis of CXCR4 antagonist ANORMED CORPORATION (CA) 2005-09-22 US claimed
US-20260130893-A1 PRMT5 INHIBITORS AND USES THEREOF GILEAD SCIENCES INC (US) 2026-05-14 US disclosed
EP-4735445-A1 KRAS MODULATING COMPOUNDS GILEAD SCIENCES, INC. (US) 2026-05-06 EP disclosed
EP-4735453-A1 KRAS MODULATING COMPOUNDS GILEAD SCIENCES, INC. (US) 2026-05-06 EP disclosed
US-20260116987-A1 ANTIBODIES AND FUSION PROTEINS THAT BIND TO CCR8 AND USES THEREOF GILEAD SCIENCES INC (US) 2026-04-30 US disclosed
WO-2026090160-A2 CD4-TARGETED IL-15 MOLECULES AND METHODS OF USE GILEAD SCIENCES, INC. (US) 2026-04-30 WO disclosed
WO-2026089992-A1 PRMT5 INHIBITORS AND USES THEREOF GILEAD SCIENCES, INC. (US) 2026-04-30 WO disclosed
WO-2006020891-A2 CHEMOKINE COMBINATIONS TO MOBILIZE PROGENITOR/STEM CELLS ANORMED INC. (CA) 2006-02-23 WO disclosed
US-20060035829-A1 Chemokine combinations to mobilize progenitor/stem cells ANORMED INC. 2006-02-16 US disclosed
US-20050209277-A1 Process for the synthesis of CXCR4 antagonist ANORMED CORPORATION (CA) 2005-09-22 US disclosed
WO-2004106493-A2 CHEMOKINE RECEPTOR BINDING HETEROCYCLIC COMPOUNDS WITH ENHANCED EFFICACY ANORMED INC. (CA) 2004-12-09 WO disclosed
US-20040019058-A1 Chemokine receptor binding heterocyclic compounds with enhanced efficacy ANORMED CORPORATION (CA) 2004-01-29 US disclosed
US-20030220341-A1 Chemokine receptor binding heterocyclic compounds with enhanced efficacy ANORMED, INC. (CA) 2003-11-27 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 (7 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-20080167341-A1 CHEMOKINE RECEPTOR BINDING HETEROCYCLIC COMPOUNDS WITH ENHANCED EFFICACY CCR5, CXCR4, CXCR3 CXCR4 2/4885CHRM2 2757/4885CYP2D6 3057/4885
US-20050209277-A1 Process for the synthesis of CXCR4 antagonist CXCR4, CXCR1, CXCL12 CXCR4 1/4885CHRM2 2228/4885CYP2D6 1779/4885
US-20030220341-A1 Chemokine receptor binding heterocyclic compounds with enhanced efficacy CCR5, CXCR4, CXCR3 CXCR4 2/4885CHRM2 2757/4885CYP2D6 3057/4885
US-20260116987-A1 ANTIBODIES AND FUSION PROTEINS THAT BIND TO CCR8 AND USES THEREOF CCR8, VSIG8, CCR3 CXCR4 61/4885CHRM2 3068/4885CYP2D6 3318/4885
US-20060035829-A1 Chemokine combinations to mobilize progenitor/stem cells CXCL12, CXCR2, CXCR4 CXCR4 3/4885CHRM2 2486/4885CYP2D6 4178/4885
US-20260130893-A1 PRMT5 INHIBITORS AND USES THEREOF PRMT5, PRMT1, PRMT6 CXCR4 3851/4885CHRM2 2728/4885CYP2D6 3755/4885
US-20040019058-A1 Chemokine receptor binding heterocyclic compounds with enhanced efficacy CCR5, CXCR4, CXCR3 CXCR4 2/4885CHRM2 2757/4885CYP2D6 3057/4885

“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.