SCHEMBL29425230

SCHEMBL29425230

CC(=O)NC1C(O)CC(OP(=O)([O-])OC[C@H]2O[C@@H](n3ccc(N)nc3=O)[C@H](O)[C@@H]2O)(C(=O)O)OC1C(O)C(O)CO.[Na+]

nearest known ligand 0.56

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 3)

geneUniProtsupporting neighboursconfidence
ST6GAL1 P15907 15/20 0.56
TSHR P16473 1/20 0.50
GLA P06280 1/20 0.50

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
SCHEMBL29377374 1.00 ST6GAL1 (0.56) ST6GAL1TSHRGLA
SCHEMBL29425217 1.00 ST6GAL1 (0.56) ST6GAL1TSHRGLA
SCHEMBL4181237 0.95 ST6GAL1 (0.56) ST6GAL1TSHRGLA
SCHEMBL607765 0.95 ST6GAL1 (0.56) ST6GAL1TSHRGLA
SCHEMBL584780 0.95 ST6GAL1 (0.56) ST6GAL1TSHRGLA
SCHEMBL29636269 0.95 ST6GAL1 (0.56) ST6GAL1TSHRGLA
SCHEMBL23188753 0.93 ST6GAL1 (0.49) ST6GAL1TSHRGLA
SCHEMBL122854 0.93 ST6GAL1 (0.49) ST6GAL1TSHRGLA
SCHEMBL18812503 0.93 ST6GAL1 (0.49) ST6GAL1TSHRGLA
SCHEMBL13210237 0.93 ST6GAL1 (0.49) ST6GAL1TSHRGLA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4702138-A1 PRODUCTION OF A NEGATIVELY CHARGED OLIGOSACCHARIDE BY A CELL Inbiose N.V. (BE) 2026-03-04 EP claimed
US-20250197905-A1 LEGIONAMINIC ACID GLYCOSYLTRANSFERASES FOR CHEMOENZYMATIC SYNTHESIS OF GLYCANS AND GLYCOCONJUGATES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2025-06-19 US claimed
CN-120020261-A Method for total synthesis of N-glycan 中国科学院上海药物研究所 2025-05-20 CN claimed
CN-119384513-A Novel sialyltransferases for in vivo synthesis of LST-c 帝斯曼知识产权资产管理有限公司 2025-01-28 CN claimed
WO-2024223815-A1 PRODUCTION OF A NEGATIVELY CHARGED OLIGOSACCHARIDE BY A CELL INBIOSE N.V. (BE) 2024-10-31 WO claimed
EP-4448734-A1 PRODUCTION OF ALPHA-1,3-FUCOSYLATED COMPOUNDS Inbiose N.V. (BE) 2024-10-23 EP claimed
EP-4448781-A1 PRODUCTION OF ALPHA-1,4-FUCOSYLATED COMPOUNDS Inbiose N.V. (BE) 2024-10-23 EP claimed
EP-4370664-A1 LACTO-N-BIOSE CONVERTING FUCOSYLTRANSFERASES Inbiose N.V. (BE) 2024-05-22 EP claimed
EP-4347856-A2 METHODS FOR PRODUCING TRYPTAMINE DERIVATIVES Octarine Bio ApS (DK) 2024-04-10 EP claimed
CN-117222736-A Cellular production of biological products 因比奥斯公司 2023-12-12 CN claimed
WO-2023110994-A1 PRODUCTION OF ALPHA-1,4-FUCOSYLATED COMPOUNDS INBIOSE N.V. (BE) 2023-06-22 WO claimed
EP-4192969-A1 PRODUCTION OF AN OLIGOSACCHARIDE MIXTURE BY A CELL Inbiose N.V. (BE) 2023-06-14 EP claimed
EP-4192945-A1 CELLULAR PRODUCTION OF SIALYLATED DI- AND/OR OLIGOSACCHARIDES Inbiose N.V. (BE) 2023-06-14 EP claimed
CN-116249781-A Production of biological products containing GlcNAc in cells 因比奥斯公司 2023-06-09 CN claimed
CN-116096911-A Production of oligosaccharide mixtures by cells 因比奥斯公司 2023-05-09 CN claimed
WO-2023285650-A1 LACTO-N-BIOSE CONVERTING FUCOSYLTRANSFERASES INBIOSE N.V. (BE) 2023-01-19 WO claimed
CN-115552026-A Enzymatic method for preparing CMP-Neu5Ac 马克斯·普朗克科学促进学会 2022-12-30 CN claimed
WO-2022248635-A2 METHODS FOR PRODUCING TRYPTAMINE DERIVATIVES. OCTARINE BIO APS (DK) 2022-12-01 WO claimed
WO-2022152915-A1 EXTRACELLULAR PRODUCTION OF GLYCOSYLATED PRODUCTS INBIOSE N.V. (BE) 2022-07-21 WO claimed
CN-114207108-A Genetically modified host cells producing glycosylated cannabinoids 奥克塔林生物制剂公司 2022-03-18 CN 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 (1 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-20250197905-A1 LEGIONAMINIC ACID GLYCOSYLTRANSFERASES FOR CHEMOENZYMATIC SYNTHESIS OF GLYCANS AND GLYCOCONJUGATES FNTA, MAGT1, FNTB ST6GAL1 30/4885TSHR 2722/4885GLA 451/4885

“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.