Adenosine Phosphate

Adenosine Phosphate

SCHEMBL145417

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

nearest known ligand 0.83

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 Phosphate. 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 0.83
▸ P2RY2 known ✓ P41231 3/20 0.83
▸ ADORA1 known ✓ P30542 1/20 0.83
▸ PDE4D known ✓ Q08499 1/20 0.83
▸ PDE3A known ✓ Q14432 1/20 0.83
▸ P2RY11 Q96G91 3/20 0.83
▸ SRC P12931 2/20 0.83
▸ SMN1; SMN2 Q16637 2/20 0.83
▸ TRPM2 O94759 2/20 0.83
▸ TAS1R3 Q7RTX0 2/20 0.83
▸ TAS1R1 Q7RTX1 2/20 0.83
▸ DNPH1 O43598 1/20 0.83
▸ PRKAB2 O43741 1/20 0.83
▸ LDHA P00338 1/20 0.83
▸ ADRB2 P07550 1/20 0.83
▸ FBP1 P09467 1/20 0.83
▸ PRKAG1 P54619 1/20 0.83
▸ PRKAA2 P54646 1/20 0.83
▸ KCNH2 Q12809 1/20 0.83
▸ PRKAA1 Q13131 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
Adenosine Phosphate SCHEMBL1356934 1.00 P2RY1 (0.83) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL29364783 1.00 P2RY1 (0.83) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL353218 1.00 P2RY1 (0.83) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL9068130 0.99 P2RY1 (0.81) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL1164292 0.99 P2RY1 (0.81) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL23093554 0.99 P2RY1 (0.81) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL5600449 0.99 P2RY1 (0.81) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL7064977 0.99 P2RY1 (0.81) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL5434021 0.99 P2RY1 (0.81) P2RY1P2RY11P2RY2SRCSMN1; SMN2
Adenosine Phosphate SCHEMBL1164224 0.99 P2RY1 (0.81) P2RY1P2RY11P2RY2SRCSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026043843-A1 TETRAHYDROPYRIMIDINE (THP) IONIZABLE LIPIDS FOR EFFICIENT MRNA DELIVERY THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION ON BEHALF OF THE UNIVERSITY OF NEVADA, (US) 2026-02-26 — — WO claimed
WO-2024215771-A1 SUBSTITUTED PHENYL ETHYNYL PYRIMIDINES AS POTENT INHIBITORS OF ALPHAVIRUSES SOUTHERN RESEARCH INSTITUTE (US) 2024-10-17 — — WO claimed
EP-4262812-A1 6-AZA-NUCLEOSIDE PRODRUGS AS ANTIVIRAL AGENTS FOR TREATING VIRUS INFECTIONS Southern Research Institute (US) 2023-10-25 — — EP claimed
WO-2023122212-A2 SUBSTITUTED PHENYL ETHYNYL PYRIDINE CARBOXAMIDES AS POTENT INHIBITORS OF SARS VIRUS SOUTHERN RESEARCH INSTITUTE (US) 2023-06-29 — — WO claimed
EP-4125845-A1 NOVEL 2-PYRIMIDONE ANALOGS AS POTENT ANTIVIRAL AGENTS AGAINST ALPHAVIRUSES Southern Research Institute (US) 2023-02-08 — — EP claimed
EP-4021413-A1 LIPOSOMAL TROPONOID COMPOUND FORMULATIONS United States Government as Represented by The Department of Veterans Affairs (US) 2022-07-06 — — EP claimed
WO-2022133323-A1 6-AZA-NUCLEOSIDE PRODRUGS AS ANTIVIRAL AGENTS FOR TREATING VIRUS INFECTIONS SOUTHERN RESEARCH INSTITUTE (US) 2022-06-23 — — WO claimed
CN-114469912-A Use of endoxinolate in preparation of medicine for treating diseases caused by novel coronavirus 中山亿维迪科技有限公司 2022-05-13 — — CN claimed
CN-114432282-A Application of tamoxifen in preparation of novel coronavirus resistant drugs 武汉大学 2022-05-06 — — CN claimed
CN-114432287-A Application of ITF2357 in preparation of medicine for preventing and treating coronavirus 中国科学院深圳先进技术研究院 2022-05-06 — — CN claimed
US-20040131628-A1 Nucleic acids for the treatment of disorders associated with microorganisms BRATZLER ROBERT L (US) 2004-07-08 — — US claimed
EP-1434602-A2 CPG FORMULATIONS AND RELATED METHODS Merial Limited (US) 2004-07-07 — — EP claimed
US-20040092583-A1 Treatment for inhibiting neoplastic lesions SHANAHAN-PRENDERGAST ELIZABETH (IE) 2004-05-13 — — US claimed
US-20040077601-A1 Methods and compositions relating to isoleucine boroproline compounds POINT THERAPEUTICS, INC. 2004-04-22 — — US claimed
WO-2004004658-A2 METHODS AND COMPOSITIONS RELATING TO ISOLEUCINE BOROPROLINE COMPOUNDS POINT THERAPEUTICS, INC. (US) 2004-01-15 — — WO claimed
EP-1351678-A2 TREATMENT FOR INHIBITING NEOPLASTIC LESIONS USING INCENSOLE AND/OR FURANOGERMACRENS Shanahan-Prendergast, Elizabeth (IE) 2003-10-15 — — EP claimed
US-6576636-B2 Treating a noncentral nervous system by administering a covalent conjugate of a C8-26, unbranched, naturally occurring fatty acid and a drug, provided the drug is not an adenosine receptor agonist/antagonist; anticarcinogenics PROTARGA, INC. 2003-06-10 — — US claimed
WO-2003030934-A2 CPG FORMULATIONS AND RELATED METHODS MERIAL LIMITED (US) 2003-04-17 — — WO claimed
WO-2002053138-A2 TREATMENT FOR INHIBITING NEOPLASTIC LESIONS USING INCENSOLE AND/OR FURANOGERMACRENS SHANAHAN-PRENDERGAST ELISABETH (IE) 2002-07-11 — — WO claimed
WO-2001097749-A2 THE USE OF SYNTHETIC, NON-HORMONAL 21-AMINOSTEROIDS AND THEREOF KOTZE, GAVIN, SALOMON (ZA) 2001-12-27 — — 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 (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-20040092583-A1 Treatment for inhibiting neoplastic lesions VHL, IDH2, AIFM2 P2RY1 933/4885P2RY2 832/4885ADORA1 3912/4885
US-20040077601-A1 Methods and compositions relating to isoleucine boroproline compounds BCAT1, BCAT2, APOB P2RY1 3990/4885P2RY2 4349/4885ADORA1 2695/4885

“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.

Send feedback