Ionositol (1,3,4,5,6) P5

Ionositol (1,3,4,5,6) P5

SCHEMBL406795

O=P(O)(O)O[C@@H]1[C@@H](OP(=O)(O)O)[C@H](OP(=O)(O)O)[C@H](O)[C@H](OP(=O)(O)O)[C@H]1OP(=O)(O)O

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
ITPR3 Q14573 8/20 0.94
ITPR2 Q14571 4/20 0.94
ITPR1 Q14643 4/20 0.94
INPPL1 O15357 1/20 0.94
AKT1 P31749 1/20 0.94
INPP5A Q14642 2/20 0.84
SMPD1 P17405 1/20 0.83

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
Ionositol (1,3,4,5,6) P5 SCHEMBL29635093 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL29635038 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL29635044 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL2710469 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL15209904 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL406796 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL5159171 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL30469421 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL13951027 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1
Ionositol (1,3,4,5,6) P5 SCHEMBL357421 1.00 ITPR3 (0.94) ITPR3ITPR2ITPR1INPPL1AKT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12569555-B2 Organically modified mineral micro-particles, methods of preparing the same and uses thereof CRODA INTERNATIONAL PLC (GB) 2026-03-10 US claimed
US-20250368948-A1 PRODUCT, SYSTEM AND METHOD OF CELL CULTIVATION BTL Healthcare Technologies a,s. 2025-12-04 US claimed
EP-3883655-B1 EMULSIONS WITH A HIGH INTERNAL OIL PHASE OREAL (FR) 2025-02-19 EP claimed
CN-119352003-A Aluminum pop can cover material passivating agent for water-based paint and preparation method thereof 广州和力表面处理技术有限公司 2025-01-24 CN claimed
CN-119310212-A Liquid quality method for rapidly detecting phytic acid and degradation products thereof in underground water 中国矿业大学 2025-01-14 CN claimed
EP-3699271-B1 GRANULE AND PELLET COMPOSITIONS COMPRISING PHYTASE AND PHYTIC ACID AND PREPARATION METHOD DANISCO US INC (US) 2024-09-25 EP claimed
EP-3989914-B1 COMPOSITION COMPRISING INGREDIENTS FOR DIC-GEL AND POLYOL OREAL (FR) 2024-07-24 EP claimed
CN-112135791-B Organically modified mineral particles, method for the production and use thereof 禾大国际股份公开有限公司 2024-01-26 CN claimed
EP-3974454-B1 METHOD FOR PREPARING HIGH-PURITY SUGAMMADEX SODIUM HEFEI BOSIKC PHARMTECH CO LTD (CN) 2024-01-10 EP claimed
US-11833234-B2 Emulsions with a high internal oil phase L'OREAL (FR) 2023-12-05 US claimed
EP-0350973-B1 Means and product for the diagnosis and therapy of tumours and for the treatment of weaknesses of the cellular and humoral immune system EHRENFELD UDO (DE) 1997-11-05 EP claimed
US-5059591-A polyene macroloid antibiotics, anthracyclines and cisplatin bonded with ligands, such as phospholipids and sterols THE LIPOSOME COMPANY, INC. (US) 1991-10-22 US claimed
EP-0180581-B1 DRUG PREPARATIONS OF REDUCED TOXICITY THE LIPOSOME COMPANY, INC. (US) 1991-08-07 EP claimed
EP-0180581-A4 DRUG PREPARATIONS OF REDUCED TOXICITY. LIPOSOME CO INC (US) 1988-04-27 EP claimed
US-4652449-A Encapsulating biological active substances into erythrocytes CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 1987-03-24 US claimed
EP-0101341-B1 PROCESS AND DEVICE FOR THE ENCAPSULATION IN ERYTHROCYTES OF AT LEAST ONE BIOLOGICALLY ACTIVE SUBSTANCE, IN PARTICULAR HEMOGLOBIN ALLOSTERIC EFFECTORS, AND ERYTHROCYTES SO OBTAINED Etablissement Public dit: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 1986-11-05 EP claimed
EP-0180581-A1 DRUG PREPARATIONS OF REDUCED TOXICITY. LIPOSOME CO INC (US) 1986-05-14 EP claimed
WO-1985005030-A1 DRUG PREPARATIONS OF REDUCED TOXICITY THE LIPOSOME COMPANY, INC. (US) 1985-11-21 WO claimed
US-4321259-A Controlled improvement of the O2 -release by intact erythrocytes STUDIENGESELLSCHAFT KOHLE MBH (DE) 1982-03-23 US claimed
EP-0001104-B1 MODIFIED INTACT ERYTHROCYTES, BLOOD OR BLOOD PRESERVES CONTAINING THEM AND PROCESS FOR THEIR PREPARATION Studiengesellschaft Kohle mbH (DE) 1981-05-20 EP 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-11833234-B2 Emulsions with a high internal oil phase OSTC, INO80C, F12 ITPR3 442/4885ITPR2 753/4885ITPR1 611/4885
US-12569555-B2 Organically modified mineral micro-particles, methods of preparing the same and uses thereof IPMK, ITPA, ITPR1 ITPR3 5/4885ITPR2 6/4885ITPR1 3/4885

“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.