Valspodar

Valspodar

SCHEMBL17879

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nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCB1

The experimentally established mechanism targets of Valspodar. 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
ABCB1 known ✓ P08183 14/20 1.00
ABCC1 P33527 2/20 1.00
ABCC2 Q92887 2/20 1.00
PPIA P62937 4/20 0.69
PPP3CA Q08209 3/20 0.69
FKBP1B P68106 2/20 0.69
MEN1 O00255 1/20 0.69
NPC1 O15118 1/20 0.69
ABCC3 O15438 1/20 0.69
GMNN O75496 1/20 0.69
USP2 O75604 1/20 0.69
SLCO2B1 O94956 1/20 0.69
ABCB11 O95342 1/20 0.69
LMNA P02545 1/20 0.69
POLB P06746 1/20 0.69
CYP3A4 P08684 1/20 0.69
MAPT P10636 1/20 0.69
RARB P10826 1/20 0.69
CYP2C9 P11712 1/20 0.69
CYP3A5 P20815 1/20 0.69

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
Valspodar SCHEMBL19499881 1.00 ABCB1 (1.00) ABCB1ABCC1ABCC2PPIAPPP3CA
Valspodar SCHEMBL19639131 1.00 ABCB1 (1.00) ABCB1ABCC1ABCC2PPIAPPP3CA
Valspodar SCHEMBL19639132 1.00 ABCB1 (1.00) ABCB1ABCC1ABCC2PPIAPPP3CA
Valspodar SCHEMBL18671913 1.00 ABCB1 (1.00) ABCB1ABCC1ABCC2PPIAPPP3CA
Valspodar SCHEMBL21118455 1.00 ABCB1 (1.00) ABCB1ABCC1ABCC2PPIAPPP3CA
Valspodar SCHEMBL24062361 1.00 ABCB1 (1.00) ABCB1ABCC1ABCC2PPIAPPP3CA
SCHEMBL29307747 0.97 ABCB1 (0.95) ABCB1ABCC1ABCC2PPIAPPP3CA
SCHEMBL22882366 0.96 ABCB1 (0.92) ABCB1ABCC1ABCC2PPIAPPP3CA
SCHEMBL25087720 0.96 ABCB1 (0.92) ABCB1ABCC1ABCC2PPIAPPP3CA
SCHEMBL24406589 0.95 ABCB1 (0.91) ABCB1ABCC1ABCC2PPIAPPP3CA

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

Appears in 6224 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12364682-B2 Use of tegaserod in preparation of anti-tumor drug QINGDAO HAIJI BIOMEDICINE CO., LTD. (CN) 2025-07-22 US claimed
US-20250152591-A1 TREATMENT OF HEMATOLOGICAL MALIGNANCIES WITH MENIN INHIBITORS AND P-GLYCOPROTEIN INHIBITORS KURA ONCOLOGY INC (US) 2025-05-15 US claimed
US-20250059301-A1 Fusion Protein Construct NORTHWESTERN UNIVERSITY 2025-02-20 US claimed
WO-2025027194-A1 A METHOD OF PREPARING AN AQUEOUS DISPERSION OF NANOPARTICLES IQ MEDICAL GMBH (DE) 2025-02-06 WO claimed
WO-2025027196-A1 A METHOD OF PRODUCING NANOPARTICLES OF A DEFINED SIZE IQ MEDICAL GMBH (DE) 2025-02-06 WO claimed
EP-4501320-A1 A METHOD OF PREPARING AN AQUEOUS DISPERSION OF NANOPARTICLES IQ medical GmbH (DE) 2025-02-05 EP claimed
US-20240415940-A1 HYALURONIDASE POLYPEPTIDE FOR USE IN THE TREATMENT OR PROPHYLAXIS OF A NEURODEGENERATIVE DISEASE PHARMACT HOLDING AG (CH) 2024-12-19 US claimed
EP-4472637-A1 TREATMENT OF HEMATOLOGICAL MALIGNANCIES WITH MENIN INHIBITORS AND P-GLYCOPROTEIN INHIBITORS Kura Oncology, Inc. (US) 2024-12-11 EP claimed
EP-4419125-A1 HYALURONIDASE POLYPEPTIDE FOR USE IN THE TREATMENT OR PROPHYLAXIS OF A NEURODEGENERATIVE DISEASE Pharmact Holding AG (CH) 2024-08-28 EP claimed
US-20240156808-A1 Compositions and methods to improve the therapeutic benefit of suboptimally chemical compounds and biological therapies including substituted camptothecins such as irinotecan and topotecan for the treatment of benign and neoplastic hyperproliferative disease conditions, infections, inflammatory and immunological diseases EDISON ONCOLOGY (US) 2024-05-16 US claimed
EP-1260233-A1 P-GLYCOPROTEIN MODIFIER-CONTAINING MEDICINAL COMPOSITIONS TO BE DELIVERED TO THE LARGE INTESTINE HISAMITSU PHARMACEUTICAL CO. INC. (JP) 2002-11-27 EP claimed
US-20020156124-A1 Chemotherapeutic microemulsion compositions of paclitaxel with improved oral bioavailability PHARMACIA & UPJOHN COMPANY 2002-10-24 US claimed
US-20020142950-A1 Methods for enhancing the bioavailability of a drug PRAECIS PHARMACEUTICALS, INC. 2002-10-03 US claimed
WO-2002064132-A2 CHEMOTHERAPEUTIC MICROEMULSION COMPOSITIONS OF PACLITAXEL WITH IMPROVED ORAL BIOAVAILABILITY PHARMACIA & UPJOHN COMPANY (US) 2002-08-22 WO claimed
EP-1232260-A2 POLYMORPHISMS IN THE HUMAN MDR-1 GENE AND APPLICATIONS THEREOF EPIDAUROS AG Biotechnologie Aktiengesellschaft (DE) 2002-08-21 EP claimed
WO-2002056692-A1 METHODS FOR MODULATING TUMOR GROWTH AND METASTASIS BRISTOL-MYERS SQUIBB COMPANY (US) 2002-07-25 WO claimed
US-20020016293-A1 Flavopiridol drug combinations and methods with reduced side effects NIH - DEITR 2002-02-07 US claimed
WO-2001080896-A2 FLAVOPIRIDOL DRUG COMBINATIONS AND METHODS WITH REDUCED SIDE EFFECTS ARCH DEVELOPMENT CORPORATION (US) 2001-11-01 WO claimed
WO-2001058470-A2 METHODS FOR ENHANCING THE BIOAVAILABILITY OF A DRUG PRAECIS PHARMACEUTICALS INCORPORATED (US) 2001-08-16 WO claimed
WO-2001009183-A2 POLYMORPHISMS IN THE HUMAN MDR-1 GENE AND APPLICATIONS THEREOF EPIDAUROS (DE) 2001-02-08 WO claimed