Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL6595413

C[C@@H](N)Cc1cc(C#N)c2c(c1)CCN2CCCOC(=O)c1ccccc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.38

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
ADRA1D known ✓ P25100 13/20 0.38
ADRA1A known ✓ P35348 13/20 0.38
ADRA1B known ✓ P35368 13/20 0.38
ADRB2 known ✓ P07550 1/20 0.36
ADRA2A known ✓ P08913 1/20 0.36
ADRA2B known ✓ P18089 1/20 0.36
ADRA2C known ✓ P18825 1/20 0.36
HTR1D known ✓ P28221 1/20 0.36
HRH1 known ✓ P35367 1/20 0.36
OPRM1 known ✓ P35372 1/20 0.36
SLC6A3 known ✓ Q01959 1/20 0.36
SCN1A P35498 1/20 0.36
SCN2A Q99250 1/20 0.36
SCN3A Q9NY46 1/20 0.36
DRD3 P35462 2/20 0.36
HTR1A P08908 1/20 0.36
DRD2 P14416 1/20 0.36
DRD1 P21728 1/20 0.36
DRD4 P21917 1/20 0.36
PTGS1 P23219 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 SCHEMBL29120481 1.00 ADRA1D (0.38) ADRA1DADRA1AADRA1BSCN1ASCN2A
Tartaric Acid SCHEMBL29358996 1.00 ADRA1D (0.38) ADRA1DADRA1AADRA1BSCN1ASCN2A
Cadaverine Tartrate SCHEMBL13730985 1.00 ADRA1D (0.38) ADRA1DADRA1AADRA1BSCN1ASCN2A
Cadaverine Tartrate SCHEMBL28639321 1.00 ADRA1D (0.38) ADRA1DADRA1AADRA1BSCN1ASCN2A
SCHEMBL16422049 0.96 ADRA1D (0.40) ADRA1DADRA1AADRA1BSCN1ASCN2A
SCHEMBL6597896 0.96 ADRA1D (0.40) ADRA1DADRA1AADRA1BSCN1ASCN2A
SCHEMBL1822655 0.96 ADRA1D (0.40) ADRA1DADRA1AADRA1BSCN1ASCN2A
SCHEMBL17516024 0.89 ADRA1D (0.39) ADRA1DADRA1AADRA1BSCN1ASCN2A
SCHEMBL13729910 0.88 ADRA1D (0.40) ADRA1DADRA1AADRA1BDRD3ADRB2
SCHEMBL22728212 0.87 ADRA1D (0.33) ADRA1DADRA1AADRA1BSCN1ASCN2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111116448-B Preparation method of indole derivative 北京鑫开元医药科技有限公司 2022-01-04 CN claimed
CN-111116448-A Preparation method of indole derivative 北京鑫开元医药科技有限公司 2020-05-08 CN claimed
CN-116242919-A Detection method of palladium element in silodosin bulk drug and preparation thereof and application of detection method 上海硕方医药科技有限公司 2023-06-09 CN disclosed
CN-111116448-B Preparation method of indole derivative 北京鑫开元医药科技有限公司 2022-01-04 CN disclosed
CN-111116448-A Preparation method of indole derivative 北京鑫开元医药科技有限公司 2020-05-08 CN disclosed
US-9932308-B2 Method for producing indoline compound UBE INDUSTRIES, LTD. (JP) 2018-04-03 US disclosed
US-20170197917-A1 METHOD FOR PRODUCING INDOLINE COMPOUND UBE INDUSTRIES, LTD. (JP) 2017-07-13 US disclosed
EP-3103794-A1 METHOD FOR PRODUCING INDOLINE COMPOUND UBE Industries, Ltd. (JP) 2016-12-14 EP disclosed
WO-2012147107-A2 NOVEL & IMPROVED PROCESSES FOR THE PREPARATION OF INDOLINE DERIVATIVES AND ITS PHARMACEUTICAL COMPOSITION MSN LABORATORIES LIMITED (IN) 2012-11-01 WO disclosed
WO-2012147019-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF SILODOSIN ORCHID CHEMICALS AND PHARAMCEUTICALS LIMITED (IN) 2012-11-01 WO disclosed
US-20040235932-A1 Ophthalmic pharmaceutical compositions Outdoor Wireless Networks LLC 2004-11-25 US disclosed
EP-1415666-A1 MEDICINAL COMPOSITIONS FOR OPTHALMIC USE Kissei Pharmaceutical Co., Ltd. (JP) 2004-05-06 EP disclosed
EP-1057813-B1 INDOLE DERIVATIVES AND MEDICINAL COMPOSITIONS CONTAINING THE SAME KISSEI PHARMACEUTICAL (JP) 2004-04-21 EP disclosed
US-6310086-B1 PREVENTION OR TREATMENT OF GLAUCOMA OR OCULAR HYPERTENSION KISSEI PHARMACEUTICAL CO., LTD. (JP) 2001-10-30 US disclosed
EP-1057813-A1 INDOLE DERIVATIVES AND MEDICINAL COMPOSITIONS CONTAINING THE SAME Kissei Pharmaceutical Co., Ltd. (JP) 2000-12-06 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 (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-20170197917-A1 METHOD FOR PRODUCING INDOLINE COMPOUND INMT, TPH1, INPP5A ADRA1D 809/4885ADRA1A 847/4885ADRA1B 817/4885
US-20040235932-A1 Ophthalmic pharmaceutical compositions ADRA1A, ADORA1, ADRA1D ADRA1D 3/4885ADRA1A 1/4885ADRA1B 5/4885

“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.