Adenosine Diphosphate

Adenosine Diphosphate

SCHEMBL29723933

Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)([O-])OP(=O)([O-])O)[C@@H](O)[C@H]1O.[Na+].[Na+]

nearest known ligand 0.78

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Adenosine Diphosphate. 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
P2RY1 known ✓ P47900 9/20 0.78
P2RY2 known ✓ P41231 3/20 0.78
ADORA1 known ✓ P30542 1/20 0.77
PDE4D known ✓ Q08499 1/20 0.77
PDE3A known ✓ Q14432 1/20 0.77
SRC P12931 2/20 0.78
SMN1; SMN2 Q16637 2/20 0.78
P2RX1 P51575 2/20 0.78
P2RX3 P56373 2/20 0.78
P2RX4 Q99571 1/20 0.78
P2RX2 Q9UBL9 1/20 0.78
ALDH1A1 P00352 1/20 0.78
P2RY11 Q96G91 3/20 0.77
TRPM2 O94759 2/20 0.77
DNPH1 O43598 1/20 0.77
PRKAB2 O43741 1/20 0.77
LDHA P00338 1/20 0.77
ADRB2 P07550 1/20 0.77
FBP1 P09467 1/20 0.77
PRKAG1 P54619 1/20 0.77

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
Adenosine Diphosphate SCHEMBL4734035 1.00 P2RY1 (0.78) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Diphosphate SCHEMBL30936667 0.99 P2RY1 (0.76) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Diphosphate SCHEMBL11579601 0.99 P2RY1 (0.76) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Diphosphate SCHEMBL29803182 0.99 P2RY1 (0.76) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Triphosphate SCHEMBL30839398 0.98 P2RY1 (0.75) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Triphosphate SCHEMBL1496269 0.98 P2RY1 (0.75) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Diphosphate SCHEMBL29444634 0.98 P2RY1 (0.78) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Diphosphate SCHEMBL28284912 0.98 P2RY1 (0.78) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Triphosphate SCHEMBL27568797 0.96 P2RY1 (0.73) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Triphosphate SCHEMBL30819483 0.96 P2RY1 (0.75) P2RY1P2RY2SRCSMN1; SMN2P2RX1

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022127326-A1 PROTEIN AND MULTI-STAGE POROUS METAL-ORGANIC FRAMEWORK COMPLEX, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 华南理工大学 2022-06-23 WO claimed
US-20260043061-A1 ENZYMATICALLY MEDIATED REACTIVE CRYSTALLIZATION OF STEVIOL GLYCOSIDES ARZEDA CORP (US) 2026-02-12 US disclosed
EP-4608984-A2 ENZYMATICALLY MEDIATED REACTIVE CRYSTALLIZATION OF STEVIOL GLYCOSIDES Arzeda Corp. (US) 2025-09-03 EP disclosed
CN-119859664-A Preparation method of glutathione 浙江工业大学 2025-04-22 CN disclosed
WO-2024216536-A1 METHOD FOR PREPARING RIBONUCLEOSIDE OR DERIVATIVE THEREOF, AND BIOLOGICAL ENZYME PREPARATION AND APPLICATION THEREOF 百瑞全球有限公司 2024-10-24 WO disclosed
US-20240301460-A1 ENZYMATIC SYNTHESIS OF 4'-ETHYNYL NUCLEOSIDE ANALOGS MERCK SHARP & DOHME LLC (US) 2024-09-12 US disclosed
US-12037623-B2 Enzymatic synthesis of 4′-ethynyl nucleoside analogs Merck, Sharp & Dohme LLC (US) 2024-07-16 US disclosed
CN-118147269-A High-flux enzymology normalization analysis method 中国科学院东北地理与农业生态研究所 2024-06-07 CN disclosed
CN-118126204-A Application of haw polysaccharide in preventing and treating non-alcoholic fatty liver and related diseases 云南农业大学 2024-06-04 CN disclosed
WO-2024092110-A2 ENZYMATICALLY MEDIATED REACTIVE CRYSTALLIZATION OF STEVIOL GLYCOSIDES ARZEDA CORP. (US) 2024-05-02 WO disclosed
US-20230183286-A1 NOVEL 3' END CAPS, 5' END CAPS AND COMBINATIONS THEREOF FOR THERAPEUTIC RNA NOVARTIS AG (CH) 2023-06-15 US disclosed
US-11466048-B2 3′ end caps, 5′ end caps and combinations thereof for therapeutic RNA NOVARTIS AG (CH) 2022-10-11 US disclosed
US-20220228184-A1 ENZYMATIC SYNTHESIS OF 4'-ETHYNYL NUCLEOSIDE ANALOGS MERCK SHARP & DOHME CORP. (US) 2022-07-21 US disclosed
WO-2022127326-A1 PROTEIN AND MULTI-STAGE POROUS METAL-ORGANIC FRAMEWORK COMPLEX, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 华南理工大学 2022-06-23 WO 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-12037623-B2 Enzymatic synthesis of 4′-ethynyl nucleoside analogs GALE, ENGASE, RNGTT P2RY1 3452/4885P2RY2 3719/4885ADORA1 1578/4885
US-20230183286-A1 NOVEL 3' END CAPS, 5' END CAPS AND COMBINATIONS THEREOF FOR THERAPEUTIC RNA RNGTT, NSUN2, NSUN3 P2RY1 3340/4885P2RY2 3347/4885ADORA1 1904/4885
US-20260043061-A1 ENZYMATICALLY MEDIATED REACTIVE CRYSTALLIZATION OF STEVIOL GLYCOSIDES MGAM, UGDH, UGGT1 P2RY1 914/4885P2RY2 549/4885ADORA1 3143/4885
US-20240301460-A1 ENZYMATIC SYNTHESIS OF 4'-ETHYNYL NUCLEOSIDE ANALOGS GALE, ENGASE, RNGTT P2RY1 3464/4885P2RY2 3736/4885ADORA1 1571/4885
US-11466048-B2 3′ end caps, 5′ end caps and combinations thereof for therapeutic RNA RNGTT, NSUN3, NSUN2 P2RY1 2998/4885P2RY2 2954/4885ADORA1 1767/4885
US-20220228184-A1 ENZYMATIC SYNTHESIS OF 4'-ETHYNYL NUCLEOSIDE ANALOGS GALE, ENGASE, RNGTT P2RY1 3464/4885P2RY2 3736/4885ADORA1 1571/4885

“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.