Ribavirin

Ribavirin

SCHEMBL379651

NC(=O)c1ncn(C2O[C@H](CO)[C@@H](O)[C@H]2O)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

IMPDH1NS5b

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 1.00
SMN1; SMN2 Q16637 3/20 1.00
ALDH1A1 P00352 3/20 1.00
TSHR P16473 2/20 1.00
ADORA1 P30542 2/20 1.00
THPO P40225 2/20 1.00
PMP22 Q01453 2/20 1.00
GLA P06280 1/20 1.00
EIF4E P06730 1/20 1.00
CYP3A4 P08684 1/20 1.00
TOP1 P11387 1/20 1.00
PNP P00491 4/20 0.76
KDM4E B2RXH2 2/20 0.56
HTT P42858 2/20 0.56
BLM P54132 2/20 0.56
TP53 P04637 2/20 0.56
MAPT P10636 2/20 0.56
TDP1 Q9NUW8 1/20 0.56
GAA P10253 1/20 0.56
HTR2C P28335 1/20 0.49

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
Ribavirin SCHEMBL1981630 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL326516 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL427229 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL14379766 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL41472 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL12758160 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL18537396 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL3954927 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL21311208 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1
Ribavirin SCHEMBL20806078 1.00 LMNA (1.00) LMNASMN1; SMN2ALDH1A1TSHRADORA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260083840-A1 METHODS FOR ABLATING MYELOID DERIVED SUPPRESSOR CELLS USING NEO-201 ANTIBODY PREC BIOLOGICS INC (US) 2026-03-26 US claimed
CN-119403836-A Methods for eliminating myeloid-derived suppressor cells using NEO-201 antibodies 精密生物制品股份有限公司 2025-02-07 CN claimed
EP-4499710-A1 METHODS FOR ABLATING MYELOID DERIVED SUPPRESSOR CELLS USING NEO-201 ANTIBODY Precision Biologics, Inc. (US) 2025-02-05 EP claimed
US-20240400714-A1 METHODS AND COMPOSITIONS FOR TARGETING TREG CELLS PREC BIOLOGICS INC (US) 2024-12-05 US claimed
US-20240384003-A1 METHODS AND COMPOSITIONS FOR TREATING HEMATOLOGICAL MALIGNANCIES PREC BIOLOGICS INC (US) 2024-11-21 US claimed
US-12037410-B2 Methods and compositions for targeting Treg cells PRECISION BIOLOGICS, INC. (US) 2024-07-16 US claimed
EP-4352103-A2 METHODS AND COMPOSITIONS FOR TREATING HEMATOLOGICAL MALIGNANCIES Precision Biologics, Inc. (US) 2024-04-17 EP claimed
WO-2023225608-A1 METHODS FOR ABLATING MYELOID DERIVED SUPPRESSOR CELLS USING NEO-201 ANTIBODY PRECISION BIOLOGICS, INC. (US) 2023-11-23 WO claimed
WO-2022246066-A2 METHODS AND COMPOSITIONS FOR TREATING HEMATOLOGICAL MALIGNANCIES PRECISION BIOLOGICS, INC. (US) 2022-11-24 WO claimed
US-20210002383-A1 METHODS AND COMPOSITIONS FOR TARGETING TREG CELLS PREC BIOLOGICS INC (US) 2021-01-07 US claimed
WO-2015143190-A1 ENHANCED ATRA-RELATED COMPOUNDS DERIVED FROM STRUCTURE-ACTIVITY RELATIONSHIPS AND MODELING FOR INHIBITING PIN1 BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2015-09-24 WO claimed
EP-2858648-A1 METHODS AND COMPOSITIONS FOR THE INHIBITION OF PIN1 Beth Israel Deaconess Medical Center, Inc. (US) 2015-04-15 EP claimed
US-20140219957-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF IMMUNE DISORDERS BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2014-08-07 US claimed
WO-2013185055-A1 METHODS AND COMPOSITIONS FOR THE INHIBITION OF PIN1 BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2013-12-12 WO claimed
WO-2012162698-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF IMMUNE DISORDERS BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2012-11-29 WO claimed
US-20100144618-A1 Compositions containing an intestinal trefoil peptide and a mucoadhesive PODOLSKY DANIEL K 2010-06-10 US claimed
US-20090226431-A1 Treatment of Cancer and Other Diseases VIANOVA LABS, INC. 2009-09-10 US claimed
US-20060189526-A1 COMPOSITIONS CONTAINING AN INTESTINAL TREFOIL PEPTIDE AND A MUCOADHESIVE THE GENERAL HOSPITAL CORPORATION 2006-08-24 US claimed
US-20060188471-A1 METHODS OF TREATING EPITHELIAL LESIONS THE GENERAL HOSPITAL CORPORATION 2006-08-24 US claimed
WO-2005004881-A1 USE OF RIBOFURANOSE DERIVATIVES AGAINST INFLAMMATORY BOWEL DISEASES ICN PHARMACEUTICALS SWITZERLAND LTD. (CH) 2005-01-20 WO claimed

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-20260083840-A1 METHODS FOR ABLATING MYELOID DERIVED SUPPRESSOR CELLS USING NEO-201 ANTIBODY CD47, SIGLEC9, LGALS1 LMNA 4078/4885SMN1; SMN2 2364/4885ALDH1A1 2065/4885
US-20090226431-A1 Treatment of Cancer and Other Diseases CYP46A1, CYP27A1, HMGCR LMNA 3457/4885SMN1; SMN2 4623/4885ALDH1A1 2790/4885

“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.