Vinpocetine

Vinpocetine

SCHEMBL7937775

CCOC(=O)C1=C[C@]2(CC)CCCN3CCc4c(n1c1ccccc41)[C@@H]32.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Vinpocetine. 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
▸ CHRM2 known ✓ P08172 1/20 0.98
▸ ADRA2A known ✓ P08913 1/20 0.98
▸ ADRA2B known ✓ P18089 1/20 0.98
▸ ADRA2C known ✓ P18825 1/20 0.98
▸ SLC6A4 known ✓ P31645 1/20 0.98
▸ DRD3 known ✓ P35462 1/20 0.98
▸ HTR2B known ✓ P41595 1/20 0.98
▸ SLC6A3 known ✓ Q01959 1/20 0.98
▸ PDE4D known ✓ Q08499 1/20 0.98
▸ KCNH2 known ✓ Q12809 1/20 0.98
▸ HRH3 known ✓ Q9Y5N1 1/20 0.98
▸ PDE1A P54750 18/20 0.98
▸ MEN1 O00255 2/20 0.98
▸ LMNA P02545 2/20 0.98
▸ KMT2A Q03164 2/20 0.98
▸ HIF1A Q16665 2/20 0.98
▸ CYP3A4 P08684 2/20 0.98
▸ KDM4E B2RXH2 1/20 0.98
▸ NR1I2 O75469 1/20 0.98
▸ ALDH1A1 P00352 1/20 0.98

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
Vinpocetine SCHEMBL20495312 1.00 PDE1A (0.98) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL50081 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL6246968 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL7947532 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL20077534 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL160952 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL21098929 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL21370424 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL20077503 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A
Vinpocetine SCHEMBL10571708 0.99 PDE1A (1.00) PDE1AMEN1LMNAKMT2AHIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2018162395-A1 VINPOCETINE HYDROCHLORIDE CO-CRYSTALS LINNEA SA (CH) 2018-09-13 — — WO claimed
WO-2018162394-A1 VINPOCETINE HYDROCHLORIDE CRYSTALLINE FORMS LINNEA SA (CH) 2018-09-13 — — WO claimed
CN-115806547-A Selected compounds for targeted degradation of BRD9 C4医药公司 2023-03-17 — — CN disclosed
CN-114746095-A HCK as therapeutic target of MYD88 mutant disease 达纳-法伯癌症研究所有限公司 2022-07-12 — — CN disclosed
CN-112996519-A Compositions and methods for organ-specific delivery of nucleic acids 德克萨斯大学系统董事会 2021-06-18 — — CN disclosed
CN-112955124-A Oral film compositions and dosage forms having precise active dissolution profiles 阿奎蒂夫疗法公司 2021-06-11 — — CN disclosed
CN-112778155-A Turcatecol derivatives and uses thereof 万春药业公司 2021-05-11 — — CN disclosed
WO-2018162394-A1 VINPOCETINE HYDROCHLORIDE CRYSTALLINE FORMS LINNEA SA (CH) 2018-09-13 — — WO disclosed
WO-2018162394-A1 VINPOCETINE HYDROCHLORIDE CRYSTALLINE FORMS LINNEA SA (CH) 2018-09-13 — — WO disclosed
WO-2018162395-A1 VINPOCETINE HYDROCHLORIDE CO-CRYSTALS LINNEA SA (CH) 2018-09-13 — — WO disclosed
WO-2018162395-A1 VINPOCETINE HYDROCHLORIDE CO-CRYSTALS LINNEA SA (CH) 2018-09-13 — — WO disclosed
US-20140221286-A1 SODIUM CHANNEL BLOCKERS REDUCE GLUCAGON SECRETION GILEAD SCIENCES, INC. 2014-08-07 — — US disclosed
US-6290994-B1 Beverage containing caffeine or theobromine and vinpocetine citrate for stimulating cerebral activity DECOX, S.L. (ES) 2001-09-18 — — US disclosed
EP-0760240-A1 NOVEL COMPOSITION STIMULATING THE CEREBRAL ACTIVITY AND BASED ON ALCALOIDS HAVING AN EBURNAMENINE NUCLEUS, AND PREPARATION METHODS Decox, S.L. (ES) 1997-03-05 — — EP disclosed
EP-0202051-B1 THERAPEUTIC COMPOSITIONS FOR ORAL ADMINISTRATION AMERICAN HOME PRODUCTS CORPORATION (US) 1991-08-21 — — EP disclosed
US-4904476-A TIMED RELEASE CAPSULES OF SPHEROIDS CONTAINING ISOSORBIDE DINITRATE; POWDER BLEND WITH CELLULOSE; ACRYLATE COATED; CARDIOVASCULAR DISORDERS AMERICAN HOME PRODUCTS CORPORATION (US) 1990-02-27 — — US disclosed
US-4794001-A CAPSULES CONTAINING SPHEROIDS OR POWDERS; COATED AND UNCOATED AMERICAN HOME PRODUCTS CORPORATION (US) 1988-12-27 — — US disclosed
US-4728512-A TIME-RELEASE CAPSULES AMERICAN HOME PRODUCTS CORPORATION (US) 1988-03-01 — — US disclosed
EP-0202051-A2 Therapeutic compositions for oral administration AMERICAN HOME PRODUCTS CORPORATION (US) 1986-11-20 — — EP 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 (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-20140221286-A1 SODIUM CHANNEL BLOCKERS REDUCE GLUCAGON SECRETION IAPP, SCNN1B, GLP1R CHRM2 1561/4885ADRA2A 186/4885ADRA2B 121/4885

“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.

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