SCHEMBL29356399

SCHEMBL29356399

Nc1ccn([C@@H]2OC(COP(=O)([O-])OP(=O)([O-])[O-])[C@@H](O)C2O)c(=O)n1.[Na+].[Na+].[Na+]

nearest known ligand 0.81

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
P2RY2 known ✓ P41231 4/20 0.66
P2RY4 known ✓ P51582 2/20 0.66
THRB known ✓ P10828 1/20 0.62
P2RY6 known ✓ Q15077 2/20 0.60
TSHR P16473 1/20 0.81
GLA P06280 1/20 0.81
ST6GAL1 P15907 10/20 0.71
LMNA P02545 1/20 0.62
MTOR P42345 1/20 0.62
MDM2 Q00987 1/20 0.62
NCOA1 Q15788 1/20 0.62
NCOA3 Q9Y6Q9 1/20 0.62
NT5E P21589 1/20 0.57

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
SCHEMBL5407898 1.00 TSHR (0.81) TSHRGLAST6GAL1P2RY2P2RY4
Potassium Ion SCHEMBL10585798 0.99 TSHR (0.80) TSHRGLAST6GAL1P2RY2P2RY4
Cystetine Triphosphate SCHEMBL9101211 0.98 TSHR (0.81) TSHRGLAST6GAL1P2RY2P2RY4
Cystetine Triphosphate SCHEMBL31405617 0.97 TSHR (0.80) TSHRGLAST6GAL1P2RY2P2RY4
Cystetine Triphosphate SCHEMBL10826769 0.97 TSHR (0.80) TSHRGLAST6GAL1P2RY2P2RY4
SCHEMBL11616961 0.94 TSHR (0.78) TSHRGLAST6GAL1P2RY2P2RY4
Cystetine Triphosphate SCHEMBL2194120 0.92 TSHR (0.79) TSHRGLAST6GAL1P2RY2P2RY4
Cystetine Triphosphate SCHEMBL11613107 0.92 TSHR (0.79) TSHRGLAST6GAL1P2RY2P2RY4
Choline SCHEMBL503814 0.92 TSHR (0.81) TSHRGLAST6GAL1P2RY2P2RY4
Cytarabine 5'-Phosphate SCHEMBL859798 0.92 TSHR (0.74) TSHRGLAST6GAL1P2RY2P2RY4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12600997-B2 Fermentative production of sialylated saccharides CHR. HANSEN A/S (DK) 2026-04-14 US claimed
EP-4686760-A1 SIALYLTRANSFERASES FOR THE SYNTHESIS OF SIALYLATED GLYCANS, GLYCOCONJUGATES AND GLYCOPROTEINS Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2026-02-04 EP claimed
US-20250263678-A1 COMPOSITIONS AND METHODS FOR DELIVERY OF RNA REJUVENATION TECHNOLOGIES, INC. (US) 2025-08-21 US claimed
EP-3350333-B2 POLYNUCLEOTIDES CONTAINING A STABILIZING TAIL REGION MODERNATX INC (US) 2025-08-06 EP claimed
US-20250243525-A1 BIOCATALYTIC MANUFACTURE OF SUGAR NUCLEOTIDES ZYMTRONIX CATALYTIC SYSTEMS, INC. (US) 2025-07-31 US claimed
US-12275973-B2 Enzymatic method for preparation of CMP-Neu5Ac Max-Planck-Gesellschaft zur Förderung der Wissenschaften e. V. (DE) 2025-04-15 US claimed
CN-119552932-A Preparation method of cytidine-5' -diphosphate 上海日冠生物科技有限公司 2025-03-04 CN claimed
EP-3337488-B1 TREATMENT AND PREVENTION OF NEISSERIA GONORRHOEAE INFECTION USING CMP-ACTIVATED NONULOSONATE ANALOG COMPOUNDS NAT RES COUNCIL CANADA (CA) 2024-12-18 EP claimed
US-20240352497-A1 ENZYMATIC METHOD FOR PREPARATION OF CMP-NEU5AC MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN E.V. (DE) 2024-10-24 US claimed
US-20240327447-A1 CHEMICAL SYNTHESIS OF CYTIDINE-5'-MONOPHOSPHO-N-GLYCYL-SIALIC ACID 89BIO, INC. (US) 2024-10-03 US claimed
WO-2023122616-A1 CHEMICAL SYNTHESIS OF CYTIDINE-5'-MONOPHOSPHO-N-GLYCYL-SIALIC ACID 89BIO, INC. (US) 2023-06-29 WO claimed
US-20230174991-A1 KDO-FREE PRODUCTION HOSTS FOR OLIGOSACCHARIDE SYNTHESIS INBIOSE N.V. (BE) 2023-06-08 US claimed
WO-2023026449-A1 METHOD FOR PRODUCING CYTIDINE 5'-DIPHOSPHATE COMPOUND 協和発酵バイオ株式会社 2023-03-02 WO claimed
WO-2023027178-A1 METHOD FOR PRODUCING CYTIDINE-5'-DIPHOSPHATE COMPOUND 協和発酵バイオ株式会社 2023-03-02 WO claimed
CN-115644334-A Preparation method of ginseng and gorgon fruit fermented beverage 江西水圣实业有限公司 2023-01-31 CN claimed
WO-2022263489-A1 NUCLEOSIDE-5 -OLIGOPHOSPHATES HAVING A CATIONICALLY-MODIFIED NUCLEOBASE F. HOFFMANN-LA ROCHE AG (CH) 2022-12-22 WO claimed
EP-4103730-A1 ENZYMATIC METHOD FOR PREPARATION OF CMP-NEU5AC Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2022-12-21 EP claimed
US-20220396761-A1 VIABLE BACTERIAL HOST CELL INBIOSE N.V. (BE) 2022-12-15 US claimed
EP-3575404-B1 FERMENTATIVE PRODUCTION OF SIALYLATED SACCHARIDES CHR HANSEN HMO GMBH (DE) 2022-10-19 EP claimed
WO-2022147039-A1 COMPOSITIONS AND METHODS FOR DELIVERY OF RNA REJUVENATION TECHNOLOGIES INC. (US) 2022-07-07 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 (3 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-20250263678-A1 COMPOSITIONS AND METHODS FOR DELIVERY OF RNA RNASE1, POLRMT, TERT P2RY2 4635/4885P2RY4 4783/4885THRB 897/4885
US-12600997-B2 Fermentative production of sialylated saccharides RNGTT, NANS, ENGASE P2RY2 3098/4885P2RY4 2219/4885THRB 913/4885
US-20240327447-A1 CHEMICAL SYNTHESIS OF CYTIDINE-5'-MONOPHOSPHO-N-GLYCYL-SIALIC ACID NEU2, NEU1, FUT5 P2RY2 839/4885P2RY4 822/4885THRB 4667/4885

“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.