Vindesine

Vindesine

SCHEMBL29370847

CC[C@]1(O)C[C@@H]2CN(CCc3c([nH]c4ccccc34)[C@@](C(=O)OC)(c3cc4c(cc3OC)N(C)[C@H]3[C@@](O)(C(N)=O)[C@H](O)[C@]5(CC)C=CCN6CC[C@]43[C@@H]65)C2)C1.O=S(=O)(O)O

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Vindesine. 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
TUBB4A known ✓ P04350 12/20 0.85
TUBB known ✓ P07437 12/20 0.85
TUBA3C known ✓ P0DPH7 12/20 0.85
TUBA1B known ✓ P68363 12/20 0.85
TUBA4A known ✓ P68366 12/20 0.85
TUBB4B known ✓ P68371 12/20 0.85
TUBB3 known ✓ Q13509 12/20 0.85
TUBB2A known ✓ Q13885 12/20 0.85
TUBB8 known ✓ Q3ZCM7 12/20 0.85
TUBA3E known ✓ Q6PEY2 12/20 0.85
TUBA1A known ✓ Q71U36 12/20 0.85
TUBA1C known ✓ Q9BQE3 12/20 0.85
TUBB6 known ✓ Q9BUF5 12/20 0.85
TUBB2B known ✓ Q9BVA1 12/20 0.85
TUBB1 known ✓ Q9H4B7 12/20 0.85
MLNR O43193 1/20 0.96
PTGS2 P35354 1/20 0.96
KCNH2 Q12809 1/20 0.96
GHSR Q92847 1/20 0.96
MAPT P10636 5/20 0.85

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
Vindesine SCHEMBL4285 1.00 MLNR (0.96) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL1650601 1.00 MLNR (0.96) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL28250735 1.00 MLNR (0.96) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL28177485 1.00 MLNR (0.96) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL29895728 1.00 MLNR (0.96) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL28186617 1.00 MLNR (0.96) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL11481610 0.99 MLNR (0.95) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL28212242 0.99 MLNR (0.95) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL16553307 0.99 MLNR (0.95) MLNRPTGS2KCNH2GHSRTUBB4A
Vindesine SCHEMBL15866615 0.98 MLNR (1.00) MLNRPTGS2KCNH2GHSRTUBB4A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250171497-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME BAUSCH HEALTH IRELAND LIMITED (IE) 2025-05-29 US disclosed
US-12311035-B2 Glymphatic delivery by manipulating plasma osmolarity UNIVERSITY OF ROCHESTER (US) 2025-05-27 US disclosed
US-20250049881-A1 FORMULATIONS OF GUANYLATE CYCLSE C AGONISTS AND METHODS OF USE JPMORGAN CHASE BANK, N.A. 2025-02-13 US disclosed
US-20250009824-A1 Oncolytic Immunotherapy by Tumor Micro-Environment Remodeling KALIVIR IMMUNOTHERAPEUTICS, INC. 2025-01-09 US disclosed
US-12146003-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same BAUSCH HEALTH IRELAND LIMITED (IE) 2024-11-19 US disclosed
EP-4424697-A2 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME Bausch Health Ireland Limited (IE) 2024-09-04 EP disclosed
US-20240287137-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME JPMORGAN CHASE BANK, N.A. 2024-08-29 US disclosed
EP-3004138-B1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME BAUSCH HEALTH IRELAND LTD (IE) 2024-03-13 EP disclosed
EP-4309673-A2 FORMULATIONS OF GUANYLATE CYCLASE C AGONISTS AND METHODS OF USE Bausch Health Ireland Limited (IE) 2024-01-24 EP disclosed
US-11834521-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same BAUSCH HEALTH IRELAND LIMITED (IE) 2023-12-05 US disclosed
US-20220280423-A1 GLYMPHATIC DELIVERY BY MANIPULATING PLASMA OSMOLARITY UNIVERSITY OF ROCHESTER (US) 2022-09-08 US disclosed
CN-108348578-B Methods for treating myeloproliferative disorders 阿塞勒隆制药公司 2022-08-09 CN disclosed
EP-4025251-A1 METHODS OF TREATMENT USING A GENETICALLY MODIFIED AUTOLOGOUS T-CELL IMMUNOTHERAPY PACT Pharma, Inc. (US) 2022-07-13 EP disclosed
US-20220152204-A1 PHOTOIMMUNOTHERAPY AND PHARMACEUTICAL AGENT USED THEREFOR SHIMADZU CORPORATION (JP) 2022-05-19 US disclosed
US-11319346-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same BAUSCH HEALTH IRELAND LIMITED (IE) 2022-05-03 US disclosed
US-20220119449-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME BAUSCH HEALTH IRELAND LIMITED (IE) 2022-04-21 US disclosed
EP-2459167-B2 SUBCUTANEOUS ANTI-HER2 ANTIBODY FORMULATION HOFFMANN LA ROCHE (CH) 2022-03-02 EP disclosed
US-20220047672-A1 COMPOSITIONS AND METHODS INVOLVING LAYILIN UNIV CALIFORNIA (US) 2022-02-17 US disclosed
EP-3946631-A1 PHOTOIMMUNOTHERAPY AND PHARMACEUTICAL AGENT USED THEREFOR Shimadzu Corporation (JP) 2022-02-09 EP disclosed
US-20220031867-A1 GLYMPHATIC DELIVERY BY MANIPULATING PLASMA OSMOLARITY NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2022-02-03 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 (6 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-12146003-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same GUCY1A1, GUCY1A2, GUCY1B1 TUBB4A 3349/4885TUBB 3481/4885TUBA3C 3064/4885
US-20250171497-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 TUBB4A 3349/4885TUBB 3481/4885TUBA3C 3064/4885
US-20220119449-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 TUBB4A 3349/4885TUBB 3481/4885TUBA3C 3064/4885
US-20240287137-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 TUBB4A 3349/4885TUBB 3481/4885TUBA3C 3064/4885
US-11319346-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same GUCY1A1, GUCY1A2, GUCY1B1 TUBB4A 3349/4885TUBB 3481/4885TUBA3C 3064/4885
US-11834521-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same GUCY1A1, GUCY1A2, GUCY1B1 TUBB4A 3349/4885TUBB 3481/4885TUBA3C 3064/4885

“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.