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ACTIVE PHARMA INGREDIENTS

2 API Suppliers, 1 USDMF, 2 NDC API, 1 Listed Suppliers

2 API Suppliers
1 USDMF
2 NDC API
1 Listed Suppliers

FINISHED DOSAGE FORMULATIONS

6 FDF Dossiers, 5 FDA Orange Book, 1 Europe

6 FDF Dossiers
5 FDA Orange Book
1 Europe

RELATED EXCIPIENT COMPANIES

2 BASF, 1 Gangwal Chemicals, 2 Microlex e.U, 4 Roquette

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2 BASF
1 Gangwal Chemicals
2 Microlex e.U
4 Roquette

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5 Film Formers & Plasticizers, 5 Coating Systems & Additives, 3 Lubricants & Glidants, 2 Fillers, Diluents & Binders, 1 Granulation, 1 Direct Compression, 1 Topical, 1 Thickeners and Stabilizers

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5 Film Formers & Plasticizers
5 Coating Systems & Additives
3 Lubricants & Glidants
2 Fillers, Diluents & Binders
1 Granulation
1 Direct Compression
1 Topical
1 Thickeners and Stabilizers

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow

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1 DATA COMPILATION #PharmaFlow

GLOBAL SALES INFORMATION

7 Annual Reports

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7 Annual Reports

PATENTS & EXCLUSIVITIES

1 US Patents

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1 US Patents

REF. STANDARDS & IMPURITIES

1 Others

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1 Others

Synopsis

ACTIVE PHARMA INGREDIENTS

API Suppliers

USDMF

CEP/COS

JDMF

EU WC

KDMF

NDC API

VMF

Listed Suppliers

API REF. PRICE (USD/KG)

$ 0

MARKET PLACE

API

FDF

0INTERMEDIATES

FINISHED DOSAGE FORMULATIONS

FDF Dossiers

FDA Orange Book

Europe

Canada

Australia

South Africa

Listed Dossiers

0 DRUGS IN DEVELOPMENT

DRUG PRODUCT COMPOSITIONS

REF. STANDARDS OR IMPURITIES

EDQM

USP

Others

PATENTS & EXCLUSIVITIES

US Patents

US Exclusivities

Health Canada Patents

DIGITAL CONTENT

Data Compilation #PharmaFlow

Stock Recap #PipelineProspector

Weekly News Recap #Phispers

News #PharmaBuzz

GLOBAL SALES INFORMATION

US Medicaid (USD)

Annual Reports (USD Million)

666

Finished Drug Prices

9 RELATED EXCIPIENT COMPANIES

19EXCIPIENTS BY APPLICATIONS

Chemistry

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Also known as: 220810-26-4, Vantas, Histrelin (acetate), Schembl18715, Chembl1200509, Dtxsid30176580

Molecular Formula

C₆₈H₉₀N₁₈O₁₄

Molecular Weight

1383.6 g/mol

InChI Key

OWAUGAMNPZHEOJ-YKZVIGSYSA-N

Histrelin Acetate is the acetate salt form of histrelin, a long-acting, synthetic nonapeptide analog of gonadotropin-releasing hormone (GnRH) with potential anti-tumor activity. Upon administration, histrelin binds to and activates GnRH receptors; prolonged administration results in pituitary GnRH receptor desensitization and inhibition of follicle stimulating hormone (FSH) and luteinizing hormone (LH) secretion, leading to a significant decline in testosterone production in males and may inhibit androgen receptor-positive tumor progression; in females, prolonged administration results in decreased estradiol production.

1 2D Structure

Histrelin Acetate

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

acetic acid;(2S)-N-[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2R)-3-(1-benzylimidazol-4-yl)-1-[[(2S)-1-[[(2S)-5-(diaminomethylideneamino)-1-[(2S)-2-(ethylcarbamoyl)pyrrolidin-1-yl]-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]-5-oxopyrrolidine-2-carboxamide

2.1.2 InChI

InChI=1S/C66H86N18O12.C2H4O2/c1-4-70-64(95)55-17-11-25-84(55)65(96)48(16-10-24-71-66(67)68)76-58(89)49(26-38(2)3)77-62(93)53(30-43-34-83(37-74-43)33-40-12-6-5-7-13-40)81-59(90)50(27-39-18-20-44(86)21-19-39)78-63(94)54(35-85)82-60(91)51(28-41-31-72-46-15-9-8-14-45(41)46)79-61(92)52(29-42-32-69-36-73-42)80-57(88)47-22-23-56(87)75-47;1-2(3)4/h5-9,12-15,18-21,31-32,34,36-38,47-55,72,85-86H,4,10-11,16-17,22-30,33,35H2,1-3H3,(H,69,73)(H,70,95)(H,75,87)(H,76,89)(H,77,93)(H,78,94)(H,79,92)(H,80,88)(H,81,90)(H,82,91)(H4,67,68,71);1H3,(H,3,4)/t47-,48-,49-,50-,51-,52-,53+,54-,55-;/m0./s1

2.1.3 InChI Key

OWAUGAMNPZHEOJ-YKZVIGSYSA-N

2.1.4 Canonical SMILES

CCNC(=O)C1CCCN1C(=O)C(CCCN=C(N)N)NC(=O)C(CC(C)C)NC(=O)C(CC2=CN(C=N2)CC3=CC=CC=C3)NC(=O)C(CC4=CC=C(C=C4)O)NC(=O)C(CO)NC(=O)C(CC5=CNC6=CC=CC=C65)NC(=O)C(CC7=CN=CN7)NC(=O)C8CCC(=O)N8.CC(=O)O

2.1.5 Isomeric SMILES

CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC2=CN(C=N2)CC3=CC=CC=C3)NC(=O)[C@H](CC4=CC=C(C=C4)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC5=CNC6=CC=CC=C65)NC(=O)[C@H](CC7=CN=CN7)NC(=O)[C@@H]8CCC(=O)N8.CC(=O)O

2.2 Synonyms

2.2.1 Depositor-Supplied Synonyms

1. 220810-26-4

2. Vantas

3. Histrelin (acetate)

4. Schembl18715

5. Chembl1200509

6. Dtxsid30176580

7. Mfcd00918679

8. 767h828

9. (des-gly10,d-his(bzl)6,pro-nhet9)-lhrh Acetate

2.3 Create Date

2008-12-10

3 Chemical and Physical Properties

Molecular Formula	C₆₈H₉₀N₁₈O₁₄
Molecular Weight	1383.6 g/mol
Hydrogen Bond Donor Count	16
Hydrogen Bond Acceptor Count	17
Rotatable Bond Count	34
Exact Mass	1382.68838962 g/mol
Monoisotopic Mass	1382.68838962 g/mol
Topological Polar Surface Area	487 Å²
Heavy Atom Count	100
Formal Charge	0
Complexity	2690
Isotope Atom Count	0
Defined Atom Stereocenter Count	9
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	2

4 Drug and Medication Information

4.1 Drug Information

1 of 2
Drug Name	Vantas
PubMed Health	histrelin
Drug Classes	Endocrine-Metabolic Agent
Active Ingredient	Histrelin acetate
Dosage Form	Implant
Route	Subcutaneous
Strength	50mg
Market Status	Prescription
Company	Endo Pharm

2 of 2
Drug Name	Vantas
PubMed Health	histrelin
Drug Classes	Endocrine-Metabolic Agent
Active Ingredient	Histrelin acetate
Dosage Form	Implant
Route	Subcutaneous
Strength	50mg
Market Status	Prescription
Company	Endo Pharm