Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL950956

O=C(O)C(O)C(O)C(=O)O.c1ccccc1.c1ccccc1

nearest known ligand 0.83

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CHRM1CHRM2CHRM3CHRM4ESR1ESR2GABRA1GABRB1GABRG2GBA1HRH1HTR1DHTR2AOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cadaverine Tartrate. 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
ESR2 known ✓ Q92731 1/20 0.36
TSHR P16473 3/20 0.83
TP53 P04637 1/20 0.44
LMNA P02545 4/20 0.43
MAPK1 P28482 1/20 0.43
KDM4E B2RXH2 2/20 0.41
CYP2C9 P11712 1/20 0.41
PDE4A P27815 1/20 0.41
NFKB1 P19838 1/20 0.39
CYP2C19 P33261 1/20 0.39
CYP2D6 P10635 1/20 0.38
SRC P12931 1/20 0.38
HIF1A Q16665 1/20 0.38
ALDH1A1 P00352 1/20 0.38
THRB P10828 1/20 0.38
RECQL P46063 1/20 0.38
OR51E2 Q9H255 1/20 0.37
POLB P06746 1/20 0.36
PKM P14618 1/20 0.36
PTPN1 P18031 1/20 0.36

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
Cadaverine Tartrate SCHEMBL9763204 1.00 TSHR (0.83) TSHRTP53LMNAMAPK1KDM4E
Cadaverine Tartrate SCHEMBL31427568 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Cadaverine Tartrate SCHEMBL1431070 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Tartaric Acid SCHEMBL29430365 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Cadaverine Tartrate SCHEMBL22768 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Tartaric Acid SCHEMBL5762 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Cadaverine Tartrate SCHEMBL1062721 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Cadaverine Tartrate SCHEMBL116846 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Cadaverine Tartrate SCHEMBL848 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9
Cadaverine Tartrate SCHEMBL29382062 0.91 TSHR (1.00) TSHRTP53LMNAKDM4ECYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10577403-B2 Modified polynucleotides for the production of secreted proteins MODERNATX, INC. (US) 2020-03-03 US disclosed
US-20190315824-A1 MODIFIED POLYNUCLEOTIDES FOR THE PRODUCTION OF SECRETED PROTEINS MODERNATX, INC. (US) 2019-10-17 US disclosed
US-8466296-B2 Compounds and processes for preparing substituted aminomethyl-2,3,8,9-tetrahydro-7H-1,4-dioxino[2,3-e]indol-8-ones LIGAND PHARMACEUTICALS (US) 2013-06-18 US disclosed
US-20110021455-A1 STERILISED SUCRALFATE GEL PIERRE FABRE DERMO-COSMETIQUE (FR) 2011-01-27 US disclosed
US-20100217012-A1 COMPOUNDS AND PROCESSES FOR PREPARING SUBSTITUTED AMINOMETHYL-2,3,8,9-TETRAHYDRO-7H-1,4-DIOXINO[2,3-e]INDOL-8-ONES NEUROGEN CORPORATION (US) 2010-08-26 US disclosed
US-5962737-A REACTING BENZALDEHYDE WITH NITROALKANE IN PRESENCE OF A TERTARY AMINE; THEN REDUCING USING LITHIUM ALUMINUM HYDRIDE WEST DANIEL DAVID (US) 1999-10-05 US disclosed
US-5830509-A Microparticle complexes with 2-amino-1-phenylpropanol materials NATURALLY SCIENTIFIC, INC. 1998-11-03 US disclosed
EP-0107825-A1 1,3,4,6,7,11b-Hexahydro-7-aryl-2H-pyrazino (2,1-alpha) isoquinolines useful as intermediates and pharmaceutical compounds and methods of preparation PENNWALT CORPORATION (US) 1984-05-09 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 (3 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-20190315824-A1 MODIFIED POLYNUCLEOTIDES FOR THE PRODUCTION OF SECRETED PROTEINS MSH2, POLRMT, SARNP ESR2 4252/4885TSHR 1159/4885TP53 370/4885
US-10577403-B2 Modified polynucleotides for the production of secreted proteins MSH2, POLRMT, SARNP ESR2 4252/4885TSHR 1159/4885TP53 370/4885
US-20100217012-A1 COMPOUNDS AND PROCESSES FOR PREPARING SUBSTITUTED AMINOMETHYL-2,3,8,9-TETRAHYDRO-7H-1,4-DIOXINO[2,3-e]INDOL-8-ONES MTNR1A, HTR3C, MTNR1B ESR2 363/4885TSHR 42/4885TP53 4158/4885

“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.