Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Myrcene. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 1/20 | 0.95 |
| ▸ | KMT2A | Q03164 | 3/20 | 0.46 |
| ▸ | ALOX15 | P16050 | 4/20 | 0.43 |
| ▸ | MEN1 | O00255 | 2/20 | 0.43 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.43 |
| ▸ | MAPT | P10636 | 2/20 | 0.41 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.41 |
| ▸ | UGT1A1 | P22309 | 1/20 | 0.41 |
| ▸ | SQLE | Q14534 | 4/20 | 0.40 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.39 |
| ▸ | ATM | Q13315 | 1/20 | 0.39 |
| ▸ | POLB | P06746 | 1/20 | 0.38 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Myrcene SCHEMBL11311399 | 1.00 | TSHR (0.95) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL3987529 | 0.98 | TSHR (1.00) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL21622 | 0.98 | TSHR (1.00) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL1867602 | 0.98 | TSHR (1.00) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL7011582 | 0.95 | TSHR (0.95) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL9709867 | 0.95 | TSHR (0.95) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL27480668 | 0.95 | TSHR (0.95) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL28396515 | 0.95 | TSHR (0.95) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL11291940 | 0.95 | TSHR (0.95) | TSHRKMT2AALOX15MEN1CYP3A4 | |
| Myrcene SCHEMBL28030445 | 0.95 | TSHR (0.95) | TSHRKMT2AALOX15MEN1CYP3A4 |
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 31 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| JP-60094976-A | — | — | None | — | — | JP | disclosed |
| JP-59225177-A | — | — | None | — | — | JP | disclosed |
| WO-2019030059-A1 | BISSILYLAMINOSILYL-FUNCTIONALIZED CONJUGATED DIENES AND METHODS FOR THEIR PREPARATION | SYNTHOS DWORY 7 SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA SPOLKA JAWNA (PL) | 2019-02-14 | — | — | WO | disclosed |
| US-5175346-A | Catalyst mixture of cuprous chloride and quaternary ammonium salt | RHONE-POULENC SANTE (FR) | 1992-12-29 | — | — | US | disclosed |
| US-4761507-A | Isomerization of linalyl halides with quaternary salts | UNION CAMP CORPORATION (US) | 1988-08-02 | — | — | US | disclosed |
| US-4754087-A | REACTING HYDROGEN HALIDE WITH TERMINAL CONJUGATED DIENE USING CUPROUS HALIDE-SALT CATALYST | RHONE-POULENC SANTE (FR) | 1988-06-28 | — | — | US | disclosed |
| US-4704489-A | TO GERANYL AND NERYL HALIDE | UNION CAMP CORPORATION (US) | 1987-11-03 | — | — | US | disclosed |
| US-4704485-A | ORGANIC QUATERNARY SALT | UNION CAMP CORPORATION (US) | 1987-11-03 | — | — | US | disclosed |
| EP-0132543-B1 | ISOMERIZATION OF ALLYLIC HALIDES WITH QUATERNARY SALTS | Union Camp Corporation (US) | 1986-10-08 | — | — | EP | disclosed |
| EP-0144498-A2 | Isomerization of allylic halides with alcohols | Union Camp Corporation (US) | 1985-06-19 | — | — | EP | disclosed |
| US-4244890-A | PREPARED BY CYCLIZATION OF NERYL AND GERANYL AMINES | SCM CORPORATION (US) | 1981-01-13 | — | — | US | disclosed |
| US-4228313-A | TO PREPARE A REARRANGED UNSATURATED HYDROCARBON | SCM CORPORATION (US) | 1980-10-14 | — | — | US | disclosed |
| US-4221742-A | Coupling reaction involving a Grignard and allylic halide | SCM CORPORATION (US) | 1980-09-09 | — | — | US | disclosed |
| US-4179468-A | Cyclic terpenoid onium salts, their preparation and uses | SCM CORPORATION (US) | 1979-12-18 | — | — | US | disclosed |
| US-4174406-A | Terpenylaminoalkanol fish toxicants | SCM CORPORATION (US) | 1979-11-13 | — | — | US | disclosed |
| US-RE29829-E | Insect repellent compositions and process having an N-substituted hydroxyalkyl amine as an active ingredient | SCM CORPORATION (US) | 1978-11-07 | — | — | US | disclosed |
| US-4056573-A | COUPLING, HYDROGENATION, SAPONIFICATION, ACID SCAVENGER, CUPROUS SALTN | SCM CORPORATION (US) | 1977-11-01 | — | — | US | disclosed |
| US-3975541-A | Insect repellent compositions having an N-substituted hydroxyalkyl amine as an active ingredient | SCM CORPORATION (US) | 1976-08-17 | — | — | US | disclosed |
| US-3933915-A | Insect repellent compositions and process having an N-substituted hydroxyalkyl amine as an active ingredient | SCM CORPORATION (US) | 1976-01-20 | — | — | US | disclosed |
| US-3932539-A | Process for preparing unsaturated terpene alcohols | SCM CORPORATION (US) | 1976-01-13 | — | — | US | disclosed |